Cards from USMLE-Rx (First Aid) Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

What is the first step to manage increased ICP in a patient who has lost consciousness and has a suspected intracranial hemorrhage

A

Intubate and ventilate the patient to protect the airway.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

How can a child inherit two copies of an allele from the same parent?

A

Uniparental disomy due to nondisjuction I/II error

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the neuropathology shown on the image?

A

Lewy bodies, seen in Lewy Body dementia or secondary to Parkison’s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What autoantibodies could cause a macrocytic anemia?

A

Pernicious anemia due to autoantibodies to gastric parietal cells causing malabsorption of vitamin B12. Often co-occurs with Hashimoto’s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What types of cancer are associated with hereditary loss of function of the RB1 gene?

A

Retinoblastoma, osteosarcoma, melanoma, brain cancer.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the mechanism of action of Octreotide? What conditions does it treat?

A

It is a somatostatin analogue used to treat esophageal varices, acromegaly, carcinoid syndrome, VIPomas.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How do you distinguish between disseminated intravascular coagulation (DIC) and immune thrombocytopenic purpura on labs?

A

DIC will have thrombocytopenia AND elevated INR and elevated PTT, whereas the most commonly for ITP there will only be isolated thrombocytopenia (platelets <150,000/mm^3)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Where are the LMNs located in the spinal cord?

A

In the anterior horns.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the function of oxyphils and where are they located?

A

Oxyphils are present in the parathyroid gland and may contribute to PTH secretion (but classically PTH is secreted by parathyroid chief cells).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What changes to thyroid hormone occur in pregnancy? What is the mechanism of these changes?

A

Overall, pregnant persons remain euthyroid because even though estrogen stimulates liver synthesis of thyroxine-binding globulin, which in turn leads to more total T4, but the amount of free T4 remains the same.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What finding on urinalysis indicates kidney involvement (pyelonephritis)?

A

WBC casts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the most common cause of cancer mortality in the US?

A

Lung Cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What organism would cause characteristic “crackling” on palpation of a swollen, tender, red injured area?

A

Clostridium perfirindens; crackling comes from the subcutaneous gas production; the bacteria produces a phospholipase which cleaves lecthin in plasma membranes of cells.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

A presentation of bilateral juvenile cateracts and bilateral hearing loss suggests which condition?

A

Neurofibromatosis type 2 (NF-2), due to a LoF mutation on chromosome 22, increasing the risk of multisystem cancer.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the location of the major blood supply to the uterus?

A

The uterine arteries and veins run along the cardinal ligament of the uterus attaching to the uterine walls above the level of the cervix.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How is gout and pseudogout differentiated on microscopy of arthrocenteis?

A

Gout = negatively birefringent needle-shaped crystals.

Psudogout = positively birefringent rhomboid crystals.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What glomerular abnormalities would be consistent with Henoch-Schonlein Purpura (HSP)?

A

Presence of mesangial IgA deposits.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What study type could be used to calculate relative risk for developing a given disease based on exposures?

A

Prospective cohort study.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Elevated levels of ketoacids in a newborn with neurologic symptoms is suggestive of what condition?

A

Maple Syrup Urine Disease—caused by deficiency in branched-chain alpha-ketoacid dehydrogenase leading to inability to metabolize isoleu, leu and val.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What is the mechanism of action of Flucytosine?

A

It is converted to 5-FU in fungal cells, thus interfering selectively with fungal DNA synthesis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

How do glucocorticoids block inflammation?

A

By inhibiting phospholipase A2, which stops the production of arachidonic acid, which acts downstream to cause prostacyclin and prostaglandin release.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Which bugs are the top causes of PID?

A

Chlamydia trachomatis and Neisseria gonorrhoeae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

What class of GPCR receptors could contribute to postural hypotension? What is the mechanism of action?

A

alpha-1 (a1) receptor blockade, with resultant decrease in phospholipase C and decrease in calcium release. A1 vasoconstricts, B2 vasodilates.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What symptoms suggest giant cell arteritis? What is GCA often accompanied by?

A

Polymyalgia rheumatica (fatigue and stiffness esp with proximal muscle weakness in hip and shoulder) often accompanies GCA; GCA symptoms include unilateral headache and vision changes (classic patient is older female).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Name one way that cancer cells can escape immune detection.

A

MHC-I downregulation (note that MHC II downregulation does not play a role in immune evasion in cancer).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

Which phospholipid is missing in neonatal respiratory distress syndrome?

A

phosphatidylcholine—the primary component of pulmonary surfactant?.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Pesticide exposure (organophosphates) would lead to what kind of symptoms? How would these be treated?

A

Symptoms: DUMBBELLS (diarrhea, urination, miosis, bronchospasm, bradycardia, excitation of skeletal muscle, lacrimation, sweating, salivation (cholinergic excess, is wet). Treated with atropine which blocks muscarinic receptors and pralidoxime in addition to binding and displacing the organophosphates from acetylcholinesterases.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

What is a differential for a rash which begins initially on the soles and palms?

A
  1. Rocky Mountain spotted fever (caused by Rickettsia ricketsii, transmitted by ticks)
  2. Meningococcemia
  3. Secondary syphilis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

What organism is associated with Guillain Barre Syndrome? What are its chacteristics?

A

Campylobacter jejuni: grows hot (42C), is a gram negative, S shaped, oxidase positive.

GBS -> rapidly progressive, ascending paralysis with muscle weakness originating in the distal lower extremities.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

What is a hapten?

A

A hapten is a moleule which can only activate an immune response when it is bound by a protein (e.g. in penicillin induced autoimmune hemolytic anemia).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

Which opioid receptors are responsible for the effects of heroin?

A

mu-receptors.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
32
Q

What is the characteristic rash in impetigo? Which organism(s) cause it?

A

Impetigo is either bullous (Staph aureus) or nonbullous (Group-A Strep OR staph aureus). The classic rash is erythematous with multiple vesicles which produce honey-coloured plaques on rupture.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
33
Q

Polyomavirus JC / JC virus presents in which population and with what symptoms?

A

JC virus can cause progressive multifocal leukoencephalopathy in patients which are immunosuppressed.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
34
Q

What changes on labs are expected in disseminated intravascular coagulation?

A

Decreased platelet count, higher bleeding time, prothrombin and partial thromboplastin (PT/PTT) time.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
35
Q

What are findings on urinalisys for post-strep glomerulonephritis? (or nephritic syndrome more generally)

A

hematuria (may have RBC casts), HTN, edema, moderate but not crazy (3.5g+) proteinuria.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
36
Q

What would explain a paradoxical high TSH and high T3 level in the context of low iodine uptake?

A

Exogenous levothyroxine (causing thyrotoxicosis factitia).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
37
Q

What are classic findings on light microscopy from a kidney biopsy in a patient with Goodpasture’s Syndrome?

A

Auto antibodies against collagen IV in glomerular basement membranes leading to glomerulonephritis (crescent formation + fibrosis). This is a nephritic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
38
Q

How would you clinically differentiate between spontaneous pneumo and tension pneumo?

A

Tension pneumo is typically associated with trauma to the chest wall which will develop tachycardia and tachypnea and eventually cardiac arrest. As well, the trachea should deviate away from the pneumo and there will be increased JVP.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
39
Q

What are the symptoms and associated organisms for reactive arthritis?

A

Typically occurs 2-3w post-infection with Shigella, yersinia, chlamydia, campylobacter, salmonella. Symptoms include asymmetric seronegative oligoarthritis, coupled with conjunctivitis and urethritis (can’t see, can’t pee, can’t bend my knee).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
40
Q

What is the impact of prostaglandin E2 on renal perfusion?

A

PgE2 causes afferent vasodilation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
41
Q

What are some examples of anti-VEGF therapies? What diseases do they treat?

A
  1. Macular degeneration (ranibizumab, pegaptanib, aflibercept)
  2. colon, breast, non-small cell lung cancer (bevacizumab)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
42
Q

Which viruses contain hemagglutinin?

A

Influenza viruses and measles virus.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
43
Q

What is the mechanism of activity of digoxin?

A

Na+intracellular concentrations increase because digoxin inhibits Na/K pump. As Na+ increases, it inhibits Na/Ca++ pump activity, causing intracelullar concentrations of Ca++ to rise (increasing contractility).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
44
Q

What is the most common cause of hereditary thrombophilia?

A

factor V Leiden mutation, causing inability of protein C to inactivate factor V, leading to continuous activation of coag pathway.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
45
Q

What pituitary condition is associated with postpartum fatigue, weight loss, amenorrhea and failure to breastfeed?

A

Sheehan syndrome (postpartum hypopituitarism) -> global decrease in prolactin, GH, FSH/LH, TSH, ACTH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
46
Q

Necrotic inflammatory infiltrate and giant cells on a bone biopsy is characteristic of…?

A

Extrapulmonary tuberculosis of the spine (Pott disease).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
47
Q

For prolonged (10y+) alcohol use disorder, what signs are expected on brain imaging?

A

Cerebellar degeneration leading to ataxia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
48
Q

What are the indications and mechanism of action of macrolides?

A

Macrolides include azithromycin, clarithromycin and erythromycin. They work by inhibiting protein synthesis by binding 23S rRNA of the prok 50S ribosome, blocking the P site. Indications are atypical pneumonia, Chlamydia, Gram+ cocci for pts allergic to penicillin and pertussis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
49
Q

What are the indications and side effects of ribavirin?

A

Ribavirin is used to treat RSV, hep C and some viral hemmhorragic fevers. It can cause a hemolytic anemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
50
Q

What are the diagnostic criteria for rheumatic fever?

A

Migratory polyarthritis, pancarditis, subcutaneous nodules, erythema marginatum (pink rings on torso and inner surface of limbs), sydenham chorea., elevated ASO (anti-streptolysin O) titre..cardiac biopsy indicates insterstitial myocardial granulomas.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
51
Q

What extra heart sounds might be heard in a patient who had acute rheumatoid fever?

A

Mitral valve stenosis: an opening snap with a diastolic rumble best appreciated over the Mitral area.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
52
Q

What is the classic presentation and causative organism of karposi sarcoma?

A

KS is caused by human herpesvirus 8; it is an AIDS-defining illness with firm palpable purple maculopapular rashes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
53
Q

How does liver cirrhosis lead to lowered platelet count?

A

Portal hypertension -> splenomegaly -> entrapment of platelets.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
54
Q

What is a classic presentation of prolactinoma?

A

Bitemporal hemianopia with diminished libido, worsening headache, gynecomastia and ED in men, decreases in muscle mass, body hair and osteopenia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
55
Q

What is the mechanism of action of bleomycin?

A

Bleomycin causes DNA breakage leading to G2 arrest.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
56
Q

Which phase of the cell cycle is affected by vincristine and paclitaxel?

A

M phase—paclitaxel promotes microtubule stabilization, vincristine destabilizes micotubules.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
57
Q

What is leucovorin?

A

Leucovorin is folinic acid, the active metabolite of folic acid. It is used to counter myelosuppression (i.e. methotrexate).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
58
Q

What is the location of the lesions and the characteristic presentation of Korsakoff psychosis?

A

Korsakoff psychosis presents as anterograde amnesia, confabulation, personality changes. Lesions occur to the mammillary bodies (part of the limbic system). It is caused by thiamine deficiency (vitamin B1)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
59
Q

What is the natural reservoir and presentation of hantavirus?

A

Hantavirus infects the deer mouse; mouse dropping and urine are primary vectors for human infection. Presentation is fever, headache, myalgia, GI upset, dizziness and chills progressing to pulmonary edema, cough and respiratory distress.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
60
Q

What electrolyte changes are expected in a thiazide diuretic?

A

Thiazide diuretics cause hypokalemia, metabolic acidosis, hyperglycemia, hyperlipidemia, hyperuricemia and hypercalcemia due to the blockage of Na+/Cl- reabsorption in the early distal convoluted tubule.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
61
Q

What is the classification for C diff? Which toxins does it produce?

A

Gram-positive spore-forming anaerobe; produces toxin A (diarrhea causing) and toxin B (cytoxic)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
62
Q

The fusion of which embryonic structures creates the palate?

A

The palatine processes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
63
Q

Which conditions lead to elevation of Anti-Jo-1 antibodies?

A

Anti-Jo-1 are specific myositis and are directed against histidyl-tRNA-synthetase.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
64
Q

What is the first line treatment for mild oral thrush?

A

Nystatin swish and swallow.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
65
Q

What are risk factors for hepatocellular carcinoma?

A

cirrhosis (alcohol abuse), hep B/C, FH, and aflatoxin (produced by Aspergillus flavus, a peanut and grain mold).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
66
Q

Which hormone can sometimes be elevated in small-cell lung cancer?

A

ADH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
67
Q

What is crigler-Najjar syndrome Type I?

A

Caused by mutations to UDP-glucuronosyltransferase, leading to inability to conjugate bilirubin. Eventually will proceed to kernicterus (bilirubin deposits in the brain leading to encephalopathy).

Type I is more severe, type II responds to phenobarbital.

Liver transplant = cure.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
68
Q

What is the classic presentation of BCC?

A

BCC presents as raised pearly borders surrounded by telangiectasias;

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
69
Q

Which receptors are targeted by benzodiazepines? What drug would you give in an overdose? What is its mechanism of action?

A

GABA-A receptors; flumazenil, a competitive antagonist.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
70
Q

What is a risk factor for SCC of the bladder in sub-Saharan Africa?

A

Helminth infection due to chronic irritation from the eggs of Schistosoma haematobium.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
71
Q

What enzyme deficiency would explain weight loss, lethargy and disphoresis in an infant who has recently been introduced to fruit juices?

A

Aldolase B, the enzyme that converts fructose-1-phosphate to substrates for gluconeogenesis. A buildup of f1-p inhibits gluconeogenesis, leading to hypoglycaemia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
72
Q

What is the most worrisome side effect of doxorubicin

A

Dilated cardiomyopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
73
Q

What are common symptoms of (mlld vs severe) hypocalcemia?

A

Mild: parasthesia, muscle cramps and perioral numbness.

Severe: carpopedal spasm, seizures, tetany.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
74
Q

How would you prevent hemorrhagic cystitis caused by cyclophosphamide?

A

Use of mesna (which provides a free thiol which binds and inactivates acrolein, an unwanted cytotoxic metabolyte respondsible for the hemorrhagic cystitis). May also be helped by increasing fluid intake.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
75
Q

Which GPCRs are targeted to treat asthma? What is the mechanism of action?

A

The Gs pathway is activated by a B2-agonist, such as albuterol; this leads to adenylyl cyclase activation, PKA activation and phosphorylation of myosin light chain kinase, which inactivates MLCK and causes smooth muscle relaxation (bronchodilation).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
76
Q

What are the long-term sequellae of untreated syphilis

A

Aortic insufficiency due to destruction of the vasa vasorum (blood vessel supply) of the ascending aorta.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
77
Q

What is the indication and mechanism of action of Zileuton?

A

Zileuton is used for chronic asthma and functions by inhibiting 5-lipoxygenase, which converts arachidonic acid into leukotrienes (potent bronchoconstrictors).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
78
Q

Which cranial nerves are affected by a vertebral artery or posterior inferior cerebellar artery dissection / thrombosis?

A

Lateral medullary syndrome: CN IX, X and XI (sparing XII since it is medial) leading to hoarseness or dysphagia. Also affects descending sympathetic fibres resulting in ipsilateral horner syndrome.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
79
Q

What symptomology should make you question a mania / bipolar I disorder diagnosis?

A

Normal sleeping (7+ hours), depression (not required to make a type I diagonsis), euthymic (not elated or expansive).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
80
Q

What is the cause and presentation of thrombotic thrombocytopenic purpura?

A

Cause is inhibition or congenital defect in ADAMTS13, an enzyme which breaks down large vWF multimers. Presentation is fever, Schistocytes (microangiopathic hemyolytic anemia), and thrombocytopenia, with normal PT and PTT, neurologic symptoms, acute kidney injury.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
81
Q

Elevated serum levels of amylase would suggest infection with which organism?

A

Something that causes parotitis, e.g. mumps.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
82
Q

What is the territory of the blood supply for the superior mesenteric artery?

A

Inferior pancreaticoduodenal artery -> head of pancreas and ascending and inferior duodenum

Branches to ileum and jejeunum,

Ileum, cecum and appendix (via ileocolic)

Right colic to ascending colon

Middle colic to transverse colon.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
83
Q

What is the indication and mechanism of action for montelukast?

A

Montelukast is a leukotriene receptor inhibitor (blocking bronchospasm without affecting leukotriene production).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
84
Q

How do you distinguish between epidural hematoma vs subdural hematoma?

A

Epidural hematoma occurs via rupture of the middle meningeal artery. Presents with a lucid interval followed by rapid deteroration and with a “lens-like” defect on CT, does not cross suture lines).

Subdural hematoma is due to rupture of bridging veins, gradual onset, crescent-shaped hemorrhage that crosses suture lines.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
85
Q

What enzyme defect would result in an infant with general weakness, a palpable liver and an enlarged cardiac silhouette on x-ray

A

lysosomal acid alpha-1,4-glucosidase; leading to accumulation of glycogen in the heart, liver and muscle.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
86
Q

What vitamin do hepatic satellite cells store?

A

Vitamin A

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
87
Q

A t(14,18) translocation leads to overexpression of what gene?

A

BCL-2; prevention of apoptosis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
88
Q

What is the pathogenesis of a syndrome involving blanching skin above the clavicle with erythema bilaterally in the upper limbs, face and neck?

A

SVC syndrome, could be a cancerous obstruction, venous thrombosis from indwelling catheter or hilar granuloma.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
89
Q

How are bronchiectasis and secondary TB differentiated on histology?

A

Bronchiectasis -> necrotizing inflammation with dilated bronchial tissue

secondary TB is caseating granulomas with central necrosis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
90
Q

How would you differentiate between a CML and a lymphoma?

A

CML -> myeloid cells (neutrophils, macrophages); a lymphoma would present with lymphadenopathy, small round blue cells interspersed with nonmalignant macrophages on splenic biopsy.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
91
Q

cells with giant granules on blood smear could indicate a defect in which gene?

A

LYST (the lysosomal trafficking regulator gene) -> phagocyte dysfunction; Chediak-Higashi syndrome.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
92
Q

UV-based DNA damage requires which repair pathway?

A

Nucleotide excision repair

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
93
Q

What is a classic presentation of sarcoidosis?

A

Resp symptoms + elevated ACE; CXR shows bilateral hilar lymphadenopathy and infiltrates. Erythema nodosum (bilateral tender red bumps on the shins). Treat with steroids.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
94
Q

How do you reverse heparin?

A

Proteamine sulfate (binds to negatively charged heparin)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
95
Q

What is the causative organism for a fishy-smelling vaginal odour with homogenous gray-white discharge without urethritis or cervicitis?

A

Gardnerella vaginalis; gram-variable pleomorphic rod.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
96
Q

What is the most common cause and characteristic presentation of B12 deficiency?

A

Pernicious anemia due to gastric parietal cell atrophy (lack of intrinsic factor). Presents as glossitis, and ascending motor and sensory loss in lower limbs, with macrocytic anemia.

NOT commonly dietary deficiency.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
97
Q

Does a decrease in cooperative oxygen binding cause a shift in the hemoglobin binding curve?

A

No.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
98
Q

What is the difference between direct inguinal hernia and indirect inguinal hernia? Which populations are they most common in?

A

Direct -> peritonium goes through the abdo wall into the inguinal triangle (common in older men).

Indirect -> peritoneum goes through the deep inguinal ring into the scrotum (common in male infants)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
99
Q

Which drugs and disease inhibit platelet aggregation via interference with GpIIIb/IIIa?

A

Abciximab, eptifibatide, tirofiban

Glanzmann thrombasthenia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
100
Q

What defense mechanism is associated with borderline personality disorder?

A

Splitting (ie. either/or classification of things as all good and all bad)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
101
Q

A glucose-6-phosphatase deficiency would present as…?

A

von Gierke disease, hepatomegaly, hypoglycemia, seizures, lactic acidosis, hypertriglyceridemia and hyperuricemia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
102
Q

What is the mechanism of action of sildenafil?

A

They inhibit PDE-5, which causes enhanced smooth muscle relaxation due to the nitric oxide. They do not increase NO levels.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
103
Q

What is the pathogenesis of the following lesion?

A

Staphylococcal scalded skin syndrome; Staph aureus releases an exotoxin which binds desmoglein-1 and interferes with desmosomes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
104
Q

What is libman-sacks endocarditis?

A

SLE -> nonbacterial thrombotic endocarditis, generally does not cause valve dysfunction or fever, emboli are composed of neutrophils, lymphocytes, fibrin and histiocytes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
105
Q

A congenital pancytopenia with bony abnormalities is suggestive of….?

A

Fanconi anemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
106
Q

Which nerve innervates the scrotum and medial thigh?

A

Ilioinguinal nerve (runs into the inguinal canal via the top of the spermatic cord).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
107
Q

What is the mechanism of action of beta-blockers for HTN?

A

Decrease in renin production by blocking beta-adrenergic receptors (which normally release renin in response to sympathetic stimulation).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
108
Q

What changes on PFT are expected in COPD?

A

Decrease in FEV

Decrease in forced Vital Capacity (FVC)

Decreased FEV1:FVC ratio

Increased Total Lung Capacity (TLC)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
109
Q

What is the mechanism of action of benzodiazepines?

A

Increased Cl- channel opening frequency in response to GABA.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
110
Q

What is the pectinate line?

A

The junction of endoderm and ectoderm just under the anal valves.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
111
Q

What receptor type mediates glucagon’s actions?

A

A GPCR (adenylyl cyclase -> cAMP); think fasted state (so “low energy”).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
112
Q

What is the mechanism of action of cyclophosphamide?

A

Cross-links DNA at guanine (alkylates)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
113
Q

What is the classic presentation and pathogenesis of Kartagener syndrome?

A

Bronchiectasis (with associated resp infections), inability to auscultate S1 and S2, situs inversus.

Kartagener syndrome is caused by a dynein arm defect that results in immotile cilia -> infertility.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
114
Q

When should you suspect multiple endocrine neoplasia type I?

A

Pituitary parathyroid and pancreatic (endocrine) tumors.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
115
Q

What kind of tumor would present as WHDA syndrome?

Watery Diarrhea

Hypokalemia

Achlorhydria

A

a VIPoma (vasoactive intestinal polypeptide) originating from the pancreas.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
116
Q

How does a meckel diverticulum appear most commonly on a technetium-99 scan?

A

Periumbilical area.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
117
Q

What is DHEA short for?

A

Dehydroepiandosterone.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
118
Q

What is the tumor marker most commonly found in hepatocellular carcinoma?

A

Alpha-fetoprotein.

(also found in yolk sac germ cell tumors)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
119
Q

Describe the order of the “zones” of the adrenal gland and associated hormone from the outside in.

A

Capsule

Zona glomerulosa - aldosterone

Zona fasciculata - cortisol and some sex hormones

Zona reticularis - sex hormones

Medulla - Catecholamines

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
120
Q

What serum abnormalities would be found in post-strep glomerulonephritis?

A

Elevated creatinine, decreased C3 levels (due to complement activation).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
121
Q

What is the most common causative organism for otitis externa (swimmer’s ear)

A

Pseudomonas aeruginosa (gram-neg, rod-shaped)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
122
Q

What is the mechanism of action of cocaine?

A

It is an indirect sympathomimetic, functions by inhibiting reuptake of dopamine, norepinephrine and serotonin specifically targeting the nucleus accumbens.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
123
Q

How does cardiac tamponade present clinically? On ECG?

A

Beck triad: hypotension, distended neck veins, distant heart sounds, tachycardia with pulsus paradoxus.

ECG would show low-voltage QRS with different amplitudes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
124
Q

What would explain a presentation of bone pain, headache, tinnitus, vertigo and hearing loss? What would you expect on labs?

A

Paget disease (abnormal bone remodelling with incraesed osteoclastic followed by osteoblastic activity). Increased alkaline phosphatase on lab.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
125
Q

Why would esmolol be preferred over metoprolol in acute arrhythmia?

A

Esmolol has a much shorter half life (9 minutes!) so it is good to trial if beta-blocker would be tolerated esp in a pt with cardiac conditions.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
126
Q

What is the drug class of choice for treating hypertriglyceridemia?

A

Fibrates e.g. gemfibrozil (the lowering in triglycerides is accompanied with small reduction in LDL and small increase in HDL).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
127
Q

What channels are blocked by amiodarone?

A

K+ channels

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
128
Q

Describe the causative organism and progression of symptoms in syphilis.

A

Painless chancre (usually on the penis in men) but may also be in the vagina or rectum in women

Maculopapular rash, condyloma lata (genital warts), lymphadenopathy hair loss, muscle aches, sore throat

Subcutaneous granulomas, neurosyphilis (dementia, personality changes), tabes dorsalis (leading to loss of proprioception and vibratory sensation).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
129
Q

What would the bone marrow of someone with multiple myeloma look like?

A

Bone marrow plasma cells -> overproduction of monoclonal IgG and destructive bone lesions -> hypercalcemia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
130
Q

What are the signs of a disseminated Neisseria meningitidis infection?

A

Hypotension, tachycardia, rapidly enlarging purpuring rash, DIC, coma.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
131
Q

What is the treatment for Wilson disease?

A

D-penicillamine (a chelating agent)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
132
Q

What metabolic defect would be associated with a child with long, thin extremities, generalized low muscle tone, developmental delay, a downward dislocation of the lens and thromboembolic events?

A

Homocystinuria caused by either cystathionine synthase or methionine synthase mutations.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
133
Q

How would you recognize a serratus anterior injury? What is the innervation of this muscle?

A

Winging of the scapula; the serratus anterior is innervated by C5,6 and 7 via the long thoracic nerve.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
134
Q

What is the biggest risk factor for placenta previa?

A

prior C-section

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
135
Q

What form of thalassemia is incompatible with life and presents with hydrops fetalis and spontaneous abortion?

A

Alpha-thalassemia with deletions of all 4 alpha-globin genes: Hb Barts.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
136
Q

What symptoms are suggestive of turner syndrome? What congenital anomaly may be present?

A

Short stature, webbed neck and dactylitis (“sausage fingers”); may have coarctation of the aorta.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
137
Q

What findings would be seen on light microscopy in diabetic glomerulonephropathy?

A

Thickening of the the glomerular basement membrane and glomerulosclerosis (kimmelstiel-Wilson nodules)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
138
Q

What is the first-line treatment for seizure prophylaxis in patients with pre-eclampsia? What signs would indicate overdose for this drug?

A

Magnesium sulfate; loss of deep tendon reflexes (hyporeflexia) and CNS depression (drowsiness)˙.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
139
Q

What is the potter sequence? What is its cause?

A

Pulmonary hypoplasia

Oligohydramnios (cause)

Twisted face (retrognathia, flattened nose, low-set ears)

Twisted skin

Extremity defects

Renal failure (in utero)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
140
Q

What is the presentation on CXR of the most worrisome side-effect of bleomycin?

A

Ground glass opacities (pulmonary fibrosis).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
141
Q

What are the risk factors for nasopharyngeal carcinoma?

A

Male, asian (especial with epstein-barr virus infection), diet of salt-cured meats and fish.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
142
Q

Dislodged pieces of cartilage and subchondral bone would be found in what kind of arthritis?

A

Osteoarthritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
143
Q

What disease process is indicated by the circled cells?

A

They are smudge cells (destroyed lymphocytes) suggestive of chronic lymphocytic leukemia or small lymphocytic leukemia (CLL/SLL) which originate from B lymphocytes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
144
Q

What nerve root would be associated with decreased sensation around the inguinal ligament?

A

L1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
145
Q

What ovarian pathology would be present in a patient with Turner syndrome?

A

Follicular dysgenesis; theca and granulosa cells are replaced with fibrous tissue, resulting in “streak ovaries”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
146
Q

What is the clinical presentation and histology of the most common benign breast mass?

A

A fibroadenoma typically presents as a small, firm and mobile mass, nontender and changes with menstruation, with no skin changes, nipple discharge or lypmadenopathy.

On histology, fibrotic interlobular stroma are found around normal structure.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
147
Q

What breast pathology matches the picture?

A

Branching fibrovascular core exending into dilated duct: intraductal papilloma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
148
Q

What disease matches the histology?

A

Large cells with clear cells -> Paget disease of the breast

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
149
Q

What disease process matches the histology?

A

Parallel arrays of small, monomorphic cells infiltrating in lines: lobular carcinoma (in situ or infiltrative)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
150
Q

What disease matches the histology?

A

Pleomorphic sheets of cells invading adjacent fibroadipose tissue; invasive ductal carcinoma (the most common breast mass in older women.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
151
Q

What are psammoma bodies? What diseases are associated with them?

A

They are laminated concentric calcific spherules.

Associated with Papilary thoyroid carcinoma, Serous ovary, Meningioma and Mesothelioma.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
152
Q

What is the classification and typical clinical presentation for Pasteurella multocida?

A

It is a gram-neg coccobacillus, found commonly in cat/dog mouth.

Rapid and aggressive infection, skin abcess with pus.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
153
Q

Cat scratches in young children may be infected by this gram-negative rod.

A

Bartonella henselae.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
154
Q

Brucella canis, commonly found in dogs, can cause what kind of illness in humans? What are risk factors for infection?

A

B. canis is a gram-negative coccobacillus, can cause fever, malaise and hepatosplenomegaly but typically only immunocompromised & blood exposure would be at high risk for infection.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
155
Q

What is the mecahism of action by which trimethoprim leads to megaloblastic anemia?

A

TMP inhibits tetrahydrofolic acid formation -> can also cause leukopenia and granulocytopenia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
156
Q

What is the cause and presentation of DiGeorge Syndrome?

A

DiGeroge = thymus agenesis due to deletion in 22q11.2 (CATCH-22)

Cardiac defects

Abnormal facies

Thymic hypoplasia (opportunistic infections, think Candida and Pnumocystis)

Cleft palate

Hypocalcemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
157
Q

What is the cause of absent tonsils and low B-cell concentrations?

A

X-linked agammaglobulinemia, caused by a recessive primary B-cell deficiency due to a mutation in Bruton’s tyrosine kinase (impairing the maturation of B cells).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
158
Q

Which spinal tract controls voluntary movement?

A

Lateral cortitcospinal tract.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
159
Q

How would you differentiate multiple myeloma from Waldenstrom macroglobulinemia?

A

Multiple myeloma leads to high levels of IgG or IgA, Neoplastic proliferation of plasma cells (characteristic clock face). CRAB (hyperCalcemia, Renal insufficiency, Anemia, lytic Bone lesions).

Waldenstrom macroglobulinemia is characterized by excessive IgM. Proliferation of plasmacytoid lymphocytes, proteinurea, hyperviscocity syndrome, Bence Jones proteins (no lytic bone lesions).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
160
Q

What are the characteristics of the infective organism most likely associated with a tricuspid diastolic murmur in a person with IV drug use history?

A

Staphylococcus aureus is a catalase positive, coagulative positive cocci.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
161
Q

What are the characteristic findings on cardiac biopsy for a patient with rheumatoid fever?

A

Ashoff bodies with activated macrophages called Anitschkow cells.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
162
Q

Describe the characteristic cell in the lung biopsy. What is the diagnosis?

A

Reed-Sternberg cell; giant tumors cells mirror images. “owl eyes”). Hodgkin lymphoma.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
163
Q

What should be done prior to splenectomy in a setting of malignant invasion?

A

Vaccination against encapsulated organisms e.g. pneumococcus and Haemophilus influenzae.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
164
Q

Identify the organism

A

Plasmodium, because of malaria.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
165
Q

What is the classic presentation of leishmaniasis

A

Ulcers of the skin, mouth, and nose, fever, lymphadenopathy splenomegaly confirmed using biopsy and transmitted by infected sand flies.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
166
Q

What is the mechanism of action of isoniazid?

A

Inhibits the synthesis of mycolic acid to build the cell wall in mycobacteria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
167
Q

What is a common side effect of vincristine?

A

Peripheral neuropathy, areflexia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
168
Q

Identify the ovarian lesion.

A

Struma ovarii; teratoma containing thyroid tissue.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
169
Q

What is an early sign and cause of myotonic dystrophy?

A

Early signs: proximal muscle weakness. Cause: it is a nucleotide repeat expansion. Muscle biopsy shows atrophy of fibers.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
170
Q

What is the characterization of herpes viruses?

A

Double-stranded linear DNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
171
Q

What drugs follow zero order elimination kinetics?

A

Phenytoin, ethanol, high dose aspirin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
172
Q

Which organs drain to the para aortic lymph nodes?

A

Testes, ovaries, kidneys, uterine fundus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
173
Q

How would you differentiate a gastric and a duodenal ulcer?

A

Gastric = worse with eating and associated with NSAID use. Must biopsy margins to r/o malignancy.

duodenal =Relief with eating. Associated with Zollinger-ellison syndrome. On histology, hyperplasia of Brunner glands.

Both strongly associated with H. pylori

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
174
Q

What are the four mature defence mechanisms?

A

Sublimation, altruism, suppression, humour

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
175
Q

How would you distinguish between a lesion of the upper trunk and lower trunk of the brachial plexus?

A

Upper trunk results in a waiters tip position due to deltoid, infraspinatus and biceps deficit (C5-C6)
lower trunk presents as a clawed hand or deficit hand muscles (C8-T1)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
176
Q

What is the pathogenesis of a complete classic mole?

A

An enucleated egg is fertilized by a single sperm, which then duplicates.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
177
Q

What disease process would explain symptoms of anemia with cola coloured urine in the morning?

A

Paroxysmal nocturnal hemoglobinuria. Caused by loss of PIGA gene required for GPI anchors for CD55 and CD59. Loss of CD55 and CD59 leads to complement-mediated hemolysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
178
Q

Identify the pathology from the bone marrow aspirate. What are the defining features?

A

Hamophagocytic lymphohistiocytosis; macrophages are overactive leading to fever, pancytopenia, hepatosplenomegaly….macrophages are shown phagocytosing marrow cells.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
179
Q

How would you distinguish between cholecystitis, large bowel seeding and PID seeding of a liver abcess

A

Cholecystitis tends to present with fever N/V.

Large bowel ascending infection will often be accompanied by bloody diarrhea

PID will show lower abdo pain and adhesions of the peritoneum to the liver (“violin string”)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
180
Q

What is the mechanism of action of ethosuximide

A

Ethosuximide is used for absence seizures and it blocks T-type calcium channels.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
181
Q

What hormone is secreted by dilated ventricles in heart failure? What are its physiologic effects (3)?

A

Brain Natriuretic Peptide (BNP), this acts on the collecting tubule to decrease Na+ reabsorption

Increases GFR by dilatation of afferent arteriole

Reduces the osmotic gradient by vasodilating the vasa recta.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
182
Q

Hyperintense lesions on FLAIR MRI may indicate what diagnosis?

A

MS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
183
Q

This kidney stone suggests infection with which microorganisms?

A

“staghorn stone” is made of ammonium magnesium phosphate, caused by infection by urease-producing bugs, eg. Proteus, Staph, Ureaplasma and Kliebsiella.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
184
Q

Which markers are Reed-Sternberg cells classically positive for?

A

CD15 and CD30

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
185
Q

Describe the typical induction treatment for acute lymphoblastic leukemia

A

vincristine, L-asparaginase, prednisone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
186
Q

What chromosomal abnormality is associated with an increased risk of acute lymphoblastic leukemia?

A

Trisomy 21

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
187
Q

Which organism causes a water diarrhea, hyponatremia and pneumonia with occasional CNS symptoms?

A

Legionella pneumophila

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
188
Q

What is the mechanism of lead poisoning toxicity?

A

Inhibition of aminolevulinic acid dehydratase and ferrochelatase leading to issues in the heme synthesis pathway (hence, microcytic anemia).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
189
Q

What is the mechanism of action of steoroid suppression of inflammation?

A

Steroids inhibit NF-kB a transcription factor for TNF-alpha and other inflammatory agents.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
190
Q

An individual on albuterol which is experiencing persistent/chronic asthma should have what added to their treatment regiment?

A

An inhaled corticosteroid (fluticasone, budesonide).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
191
Q

How would you differentiate between injury to the common peroneal, the deep peroneal and the superficial peroneal nerve?

A

Deep peroneal: inability to dorsiflex foot, foot drop

Superficial peroneal, inability to evert foot and sensory loss over lateral leg and dorsal surface of foot.

Common peroneal = both.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
192
Q

Is furosemide a good choice for treatment of hypertension

A

No. It addresses volume overload, but generally has no effect on blood pressure.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
193
Q

What is the first line of treatment for diabetic nephropathy?

A

An ACE inhibitor – it’s renoprotective!

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
194
Q

What is the presentation and cause of Prader-Willi syndrome?

A

Hyperphagia, obesity, intellectual disability, hypotonia and hypogonadism.

Occurs due to deletion or mutation of paternal copy of the gene on chromosome 15

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
195
Q

What kind of antibody is rheumatoid factor? What is its epitope?

A

IgM; Fc portion of igG

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
196
Q

Which receptors does ADH act on? What are their functions?

A

V1 increases blood pressure (vasoconstriction).

V2 lowers serum osmolarity (increases water reabsorption in collecting duct).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
197
Q

Suppose a patient is refusing a procedure and is capable of consent. What must you do before you grant the request?

A

Ensure they understand the risks and benefits of the procedures so their content is informed.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
198
Q

This patient presents with right flank pain. What is the diagnosis? What is the first line treatment?

A

Urolithiasis (kidney stones).

If hypercalciuric, then treat with hydrochlorothiazide

If gouty allopurinol would be ok.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
199
Q

What is procainamide’s effect on the heart?

A

Procainamide blocks sodium and potassium channels, acting to slow depolarization in ventricular muscle fibres.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
200
Q

What is adenosine’s effect on the heart?

A

Adenosine inhibits the SA AV and His-purkinje cell activity, decreasing conduction velocity by inhibiting L-type calcium channels.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
201
Q

What is the effect of verapamil in the heart?

A

Verapamil is a calcium channel blocker, lowers heart muscle contractility, highest specificity for heart.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
202
Q

How does HMG – CoA reductase activity affect cholesterol synthesis?

A

It is the rate limiting enzyme of cholesterol synthesis. Increases in activity result in higher cholesterol level

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
203
Q

What is the mechanism of action of fibrates?

A

Activation of peroxisome proliferator activated receptor (PPAR) which increase HDL levels by increasing synthesis of the lipoprotein A1 and A2, as well as increasing lipoprotein lipase-mediate lipolysis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
204
Q

What is the clinical presentation of Wilson disease?

A

Before age 40

Liver disease (hepatitis, liver failure, cirrhosis)

neurologic findings similar to Parkinson’s

decreased serum ceruloplasmin

Kayser-Fleischer rings (brown discoloration of the cornea)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
205
Q

What is the most common cause of acute appendicitis in children?

A

Lymphoid hyperplasia, often subsequent to a viral infection or vaccination.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
206
Q

Which area of the brain has the highest concentration of dopamine receptors?

A

:Putamen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
207
Q

What would a nitroblue tetrazolium dye reduction test be helpful for diagnosing?

A

Chronic granulomatous disease (caused by lack of NADPH oxidase activity).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
208
Q

How does infection with clostridium tetani lead to muscle spasms?

A

The tetanospasmin is a exotoxin which cleaves SNARE proteins for inhibitory neurotransmitters including GABA and glycine which results in a net increase in muscle tone.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
209
Q

Which is the most common ligament torn in and ankle sprain due to overinversion or supination of the foot?

A

The anterior talofibular ligaments

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
210
Q

What class of antidepressants can lead to a hypertensive crisis?

A

Monoamine oxidase inhibitors -> tyramine injestion -> norepinephrine release (but can’t get degraded) ^^^BP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
211
Q

What type of skewness is this?

A

Negative skew

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
212
Q

What type of skew is this?

A

Positive skew

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
213
Q

A patient has a severe flush after starting IV antibiotic treatment. Which antibiotic was administered? How would you avoid this adverse effect?

A

Vancomycin. Do a slower infusion and/or add antihistamines.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
214
Q

What is the antibiotic most associated with aplastic anemia?

A

Chloramphenicol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
215
Q

What is the classification of the causative organism for lyme disease?

A

Borrelia burgdorferi; a corkscrew-shaped spirochete

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
216
Q

What are the major acute regulators of inflammation (late phase response)?

A

IL-1, IL-6 and TNF-alpha

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
217
Q

How do you differentiate between pre-renal vs intrinsic causes of kidney failure?

A

Pre-renal, Fractional sodium excretion <= 1%; BUN:Cr >= 20

Intrinsic; Fractional sodium excretion > 2%; BUN:Cr < 15

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
218
Q

How do you calculate relative risk of developing a disease based on an exposure in a cohort study?

A

(odds of disease | exposure) / (odds of disease | not exposed)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
219
Q

What is the deficient enzyme that would result in elevated orotic acid? What is the inheritance pattern?

A

Ornithine transcarbamoylase; X-linked recessive.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
220
Q

A patient presents with hemibalismus on the right. Where is the lesion? What is the causative mechanism?

A

Left subthalamic nucleus (contralateral), often due to a lacunar stroke. The STN -> globus pallidus, which fires inhibitory GABA neurons to the thalamus.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
221
Q

What changes to LH, FSH and estrogen in menopause?

A

LH and FSH go up, estrogen goes down.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
222
Q

Where do T cells develop in the lymph nodes?

A

The paracortex.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
223
Q

This patient presents with a history of joint and abdo pain as well as loose, greasy stools. Given the biopsy of the lamina propria below, what is the causative organism? What is the stain used on the micrograph?

A

Tropheryma whipplei (whipple dissease).

Per-iodic Schiff stain showing intracellular gram +ve bacteria.

Also can get cardiac and neurologic symptoms.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
224
Q

What is the treatment of carbon monoxide poisoning?

A

Intubate if require protected airway; otherwise hyperbaric oxygen.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
225
Q

What antidote can be given for cyanide poisoning?

A

Hydroxocobalamin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
226
Q

Why must alcohol be avoided in patients taking metronidazole?

A

Metronidazole inhibits acetaldehyde dehydrogenase, consumption of alcohol leads to buildup acetaldehyde which will produce nausea, vomiting, headache, palpitations, and flushing.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
227
Q

Differentiate cluster headaches from migraines.

A

Cluster headaches: periorbital, sharp pain non-pulsatile at the same time each day. Last up to two hours and presents with autonomic symptoms including nasal congestion, lacrimation, conjunctival injection, flushing, sweating. Treat with high flow oxygen, a triptan, verapamil.
Migraine headaches: unilateral location with throbbing and pulsatile pain lasting up to 72 hours. Often accompanied by auras, nausea and vomiting, photophobia and photophobia. Maybe in improved with NSAIDs, and ergotamine, selective serotonin agonists including sumatriptan.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
228
Q

Differentiate between familial adenomatous polyposis and Lynch syndrome (non-polyposis colorectal cancer).

A

FAP presents with thousands of polyps on colonoscopy and is due to mutations in the APC gene. Lynch syndrome is due to problems in mismatch repair leading to microsatellite instability. 70% of people develop colorectal cancer and there is a high risk of endometrial, ovarian, urinary tract, small intestinal, stomach, and biliary cancer.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
229
Q

A fracture to the femoral head could disrupt blood flow to which artery?

A

The medial femoral circumflex artery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
230
Q

What pathology is present on this image? which disease is associated with it?

A

Auer rods appearing in acute promyelocytic leukemia (a type of AML)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
231
Q

What pathology is present on the image?

A

Call-exner bodies or pseudo-rosettes are spaces which appear among the granulosa cells found in granulosa cell.(Ovarian) tumors.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
232
Q

What pathology is present on this image?

A

Cowdry A inclusion bodies - intranuclear eosinophilic inclusions with a clear halo found in VZV infections.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
233
Q

What vitamin deficiency is related to this image?

A

Keratomalacia associated with vitamin A deficiency may also present with edamatous and thickened cornea.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
234
Q

What is the classification of Helicobacter pylori?

A

A gram-negative, flagellated, curved bacteria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
235
Q

Which immunosuppressant is associated with renal toxicity?

A

Cyclophosphamide

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
236
Q

What is the characteristic presentation of endometriosis

A

Endometrial tissue found outside of canal. Often in the ovaries, pelvis, or peritoneum during the menstrual phase, this tissue has outlet end will begin to accumulate for example with chocolate sis filled with reddish-brown blood in the ovaries. It is associated with cyclic and progressively worsening pelvic pain, bleeding, dysparenuia, dyschezia, and infertility

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
237
Q

What is the typical presentation of juvenile idiopathic arthritis?

A

Relapsing spiking fevers accompanied by poly articular joints, swelling, and macular salmon pink rash present anywhere in the body. Sometimes generalized lymphadenopathy and hepatosplenomegaly.

Treatment is nSAIDs, steroids, methotrexate IVIG and biologics.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
238
Q

Stage of the cell cycle sites oocytes are suspended in from birth to ovulation?

A

Prophase I

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
239
Q

Which human leukocyte antigens and for greater susceptibility to type I diabetes?

A

HLA DR4 and DR3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
240
Q

What are the characteristics of glioblastoma multiforme?

A

Most common brain cancer in adults, presents in the hemispheres with areas of necrosis and localized edema surrounded by pseudo palisading cells. Headaches, focal neurologic findings, nausea and vomiting are common.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
241
Q

What is the classic presentation for a posterior urethral injury?

A

Boggy, high riding prostate, blood at the urethral meatus, inability to insert a foley

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
242
Q

What is the genetic cause of ocularcutaneous albinism?

A

A defect in tyrosinase which impairs the ability to convert tyrosine to melanin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
243
Q

What is Waterhouse-Friderichsen Syndrome?

A

Primary adrenal failure due to Neisseria gonorrheae-caused adrenal hemorrhage. Presents with septicaemia, DIC and endotoxic shock

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
244
Q

What is the common trigger for hemolytic uremic syndrome?

A

Enterohemorrhagic E. coli infection. It’s also accompanied by diarrhea.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
245
Q

Which mutations are associated with autosomal dominant polycystic kidney disease? At what age does it typically present?

A

Polycystin 1 (Chromosome 16), less commonly polycystin 2 (chromosome 4)

Typical presentation is 20-30y

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
246
Q

What are the classic symptoms of congenital rubella infection?

A

Sensorineural hearing loss, cataracts, cardiac disease (patent ductus arteriosus).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
247
Q

Which HLA antigen is associated with rheumatoid arthritis?

A

HLA – DR4

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
248
Q

Which HLA antigen is associated with pernicious anemia and Hashimoto’s thyroiditis?

A

HLA – DR5

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
249
Q

Which diseases are associated with HLA – B27?

A

Ankylosing spondylitis, other seronegative arthropathy including psoriatic arthritis and reactive arthritis as well as inflammatory bowel disease and anterior uveitis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
250
Q

What medication would you use to treat an exogenous ACTH-secreting tumor?

A

Ketoconazole or mitotane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
251
Q

What symptoms would you expect to see in goodpasture syndrome?

A

Hemoptysis and Hematuria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
252
Q

Thiamine (B1 deficiency) can result in what electrolyte imbalance?

A

Lactic acidosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
253
Q

What metabolic disturbances would be expected in a patient being treated with furosemide?

A

Hypocalcemia, hypokalemia, hyponatremia, hypomagnesemia, metabolic alkalosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
254
Q

How would you treat an acetylsalicylic acid overdose?

A

Stabilize ABCd, add sodium bicarbonate infusion.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
255
Q

What is the causitive organism for slapped cheek disease?

A

Parvovirus B19

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
256
Q

What is the difference between brief psychotic disorder, schizophreniform disorder and schizophrenia?

A

Brief psychotic disorder < 1mo

Schizophreniform disorder 1mo to 6 mo

Schizophrenia >6mo

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
257
Q

What organelle is prominent in plasma cells?

A

Rough ER

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
258
Q

What type of cells are these? What condition are they typically found it?

A

Heart failure cells (these are hemosiderin-laden macrophages

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
259
Q

What is mittelschmerz?

A

Unilateral ovarian pain on ovulation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
260
Q

What are the risk factors for cervical cancer?

A

Early sexual activity, multiple partners, smoking, low SES

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
261
Q

How would you treat hyperthyroid in the setting of pregnancy (or when radiation is contraindicated)

A

Propylthiouracil

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
262
Q

Which enzyme is deficient in galactosemia?

A

Galactose-1-phosphate uridyltransferase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
263
Q

What is the reason why patients with SLE may have recurrent thrombosis?

A

Antiphospholipid antibody syndrome: antiphospholipid antibodies -> bind and expose platelet phospholipids to clotting factors. Antibodies will cause a paradoxical increase in PTT (exogenous pathway).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
264
Q

What drugs can cause torsades de pointes?

A

Antiarrhythmics: Quinidine (IA, III antiarrhy9thmics)

Antibiotics

Anti”C”ychotics

Antidepressents

Antiemetics (ondansetron)

Predisposition in long QT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
265
Q

A patient undergoing treatment for cancer presents with new onset hyperglycemia. What is the most likely cause?

A

Prednisone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
266
Q

What type of murmur is heard in an Atrial Septal Defect?

A

ASD presents with a pulmonic systolic heart murmur with a wide fixed split S2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
267
Q

What type of murmur is heard in a patent ductus arteriosus?

A

PDA presents with a machinelike continuous murmur in the left infraclavicular lesion, often with tachy, dyspnea, poor growth.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
268
Q

What amino acid deficiency can lead to pellagra?

A

Tryptophan (hartnup disease)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
269
Q

What is globus sensation?

A

A psychological disorder in which a patient feels a lump in their throat; often follows a significant life stressor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
270
Q

Which medications are used to treat late-stage prostate cancer?

A

Leupromide — a GNRH analog (suppresses LH)

Flutamide — a nonsteroidal antiandrogen

Adjuvant radiotherapy in high-risk and metastatic disease.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
271
Q

How would you differentiate between asbestosis and coal workers’ pneumoconiosis?

A

Coal miner’s disease -> look for “black, sooty lung”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
272
Q

What does this lung image show? Which disease is associated with it?

A

Ferruginous bodies (dumbbell like, rusty red), a sign of asbestosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
273
Q

What anatastomosis is associated with esophageal varices?

A

Left gastric vein into the esophageal vein

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
274
Q

How do you distinguish between someone who has been vaccinated vs someone who has been exposed to HepB

A

(+)anti-HBc indicates prior infection.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
275
Q

Hepatitis A and E are what kind of viruses?

A

Single-stranded, linear RNA viruses.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
276
Q

What is the cause that you would suspect in a child with Gower sign and calf pseudohypertrophy?

A

Duchenne Muscular Dystrophy (Gower = using arm to pull oneself up).

Often caused by frameshift mutation leading to deletion of one or more exons of the DMD gene.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
277
Q

How do you differentiate between HUS and DIC?

A

HUS = hemolytic anemia, acute kidney failure, thrombocytopenia but no change to PT/INR or PTT.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
278
Q

What type of medium is used to culture Bordatella pertussis?

A

Bordet-gengou or Regan-Lowe

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
279
Q

What type of medium is used to culture Corynebacterium diptheriae

A

Lôffler medium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
280
Q

What grows on Thayer-Martin medium?

A

Neisseria gonorrhoeae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
281
Q

How would you culture Haemophilus influenzae?

A

Chocolate agar with factor V and X

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
282
Q

What is the cause of medication-induced hemolytic anemia?

A

G6PD deficiency leading to sensitivity to oxidant drugs (e.g. antimalarials) or infections.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
283
Q

Which hair cells in the organ of corti are associated with higher pitched sounds?

A

Those at the proximal end (closest to the oval window)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
284
Q

What are the findings on EM / IF in poststreptococcal glomerulonephritis?

A

Dense humps on epithelial side of glomerular basement membrane (EM)

Granular pattern “lumpy bumpy” on IF

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
285
Q

Which translocation is associated with burkitt lymphoma?

A

T(8;14) involving c-myc into immunoglobin heavy chain locus, leading to constitutive c-myc expression.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
286
Q

What effect on volumes does mannitol have?

A

Mannitol can be used to pull fluid into the intravascular space; it is used to treat increased ICP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
287
Q

What is the effect of triamterene?

A

It is a potassium-sparing diuretic used when spironolactone is not tolerated

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
288
Q

What kidney pathology is shown in the image? What are the causes?

A

membranous nephropathy

Thickening of capillaries glomerular basement membrane on LF, spike and dome on EM.

Primary disease can be due to antibodies to phospholipase A2 (poor prognosis)

Secondary occurs with drugs, infections, SLE, solid tumors.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
289
Q

What kidney pathology is shown on the image?

A

Membranoproliferative glomerulonephritis

Mesangial proliferation, thickening of the basement membrane

May present with mixed nephritic / nephrotic signs.

Has low C3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
290
Q

What is the normal function of retinoblastoma protein?

A

prevents cell from progressing through G1/S checkpoint.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
291
Q

Where are melanocytes found?

A

In the basal layer of the epidermis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
292
Q

What conditions involve defective Type IV collagen?

A

Goodpasture syndrome and Alport syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
293
Q

What immune cells are found in the crypts of Lieberkuhn?

A

Paneth cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
294
Q

What is the function of Chief cells?

A

Pepsinogen secretion.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
295
Q

What is the function of I cells?

A

Cholecystokinin release (stimulates secretion of pancreatic enzymes and HCO3)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
296
Q

What is the function of S cells?

A

Secretin (increases pancreatic and biliary HCO3 secretion)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
297
Q

What is the cause of megacolon and failure to pass meconium with bilious vomiting in a neonate?

A

Hirschsprung disease (failure of neural crest cell migration leading to missing Auerbach and Meissner plexuses)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
298
Q

What hormone is responsible for the development of male external genetalia in utero?

A

Dihydrotestosterone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
299
Q

Hexagonal crystals forming kidney stones are most indicative of what pathology?

A

Cystine reabsorption problem causing cystinuria.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
300
Q

Radiolucent stones with rhomboid crystals are indicative of what source?

A

Uric acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
301
Q

What are the 3 types of radiopaque stones?

A

Calcium oxalate (dumbbell), Calcium phosphate (wedge-shaped). Think low-sodium diet and thiazides.

Ammonium magnesium phosphate (struvite, coffin-lid, think bugs).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
302
Q

A lactose fermentation test (MacConkey agar) would be most helpful for differentiating which bacteria?

A

Enterobacteriaceae:

Escherchia and Klebsiella ferment lactose

Salmonella and Shigella do not.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
303
Q

What are common causes of secondary hypertensive crises?

A

Anything that causes renal artery stenosis: atherosclerosis, fibromuscular dysplasia, CKD, hyperaldosteronism.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
304
Q

What congenital abnormality can occur in babies whose moms are undergoing lithium treatment?

A

Ebstein anomaly (tricuspid valve is lower into the RV, big RA, small RV).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
305
Q

What is the common presentation of leptospirosis & Weil disease?

A

Leptospira interrogans (from contaminated water) leads to flu-like symptoms, calf myalgia, jaundice and conjunctivial suffusion. Weil disease is the more severe form with renal failure and hepatitis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
306
Q

How do you differentiate hemophilia A / B from hemophilia C?

A

Hemophilia A (factor VIII) and B (factor IX) may present with bleeding into deep soft tissues and hemarthrosis. Hemophilia C has less spontaneous bleeding (factor XI) and it is more common in Ashkenazi Jews, but still very rare. All show abnormal PTT but normal PT.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
307
Q

How does the botulinum toxin get into cells?

A

Retrograde transport along axonal microtubules via dynein.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
308
Q

What is orlistat used for?

A

Orlistat is used for weight loss in patients BMI >30 (27 with comorbid conditions). It inhibits lipase -> fat loss.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
309
Q

What is the abnormality? What causes it?

A

Horseshoe kidney due to fusion at the bases of the two kidneys. The inferior mesenteric artery stops the kidneys from rising to their normal level.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
310
Q

Describe the effects of angiotensin II on the afferent and efferent arterioles.

A

It vasoconstricts both, but the efferent arteriole more, so under low dosage they will increase GFR. At high doses, it decreases GFR by constricting both afferent and efferent arterioles the same.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
311
Q

How does total peripheral resistance change in a traumatic bleed?

A

TPR is increased as the body responds to a fall in blood pressure by vasoconstriction.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
312
Q

Differentiate coagulative from liquefactive necrosis

A

Coagulative (*most organs*) cell outlines present but absent nuclei

Liquefactive (lung, brain) release of enzymes degrades tissue producing a glob.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
313
Q

Which diseases are associated with Schistosoma?

A

S. haematobium -> chronic inflammation of bladder

S. mansoni -> intestinal schistosomiasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
314
Q

Are cerebellar infarcts ipsilateral or contralateral to the lesion?

A

Ipsilateral defecit (double-crossover, once above the red nucleus and again below the red nucleus)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
315
Q

What is covered by medicare part A?

A

Hospital insurance, home hospice care + nursing homes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
316
Q

What is covered by medicare part B?

A

Basic medical bills (doctors offices, diagnostic testing)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
317
Q

What is covered by medicare part C?

A

Combo: A + B delivered by private companies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
318
Q

What is covered by medicare part D?

A

prescription Drugs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
319
Q

Fetal screening with an elevated level of alpha-fetoprotein is concerning for what congenital malformation?

A

Open neural tube defect (meningocele, myelomeningocele, encephalocele or anencephaly).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
320
Q

What changes on fetal screening raise suspicion of trisomy 18?

A

decreased alpha-fetoprotein, estriol AND beta-hCG

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
321
Q

What changes on fetal screening are suspicious for trisomy 21?

A

Decreased alpha-fetoprotein and estriol

Increased inhibin A and beta-hCG

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
322
Q

What diabetes medication can result in lactic acidosis?

A

Metformin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
323
Q

What characteristics would you expect of the skin lesion with the following biopsy?

A

Fleshy-coloured pearly papules with central telangiectasia - a Basal Cell Carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
324
Q

Identify the organism on this gram stain.

A

Candida albicans

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
325
Q

What symptoms can accompany Candida vulvovaginitis in immunocompromised patients?

A

Esophagitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
326
Q

How would you clinically differentiate between gonorrhea and candidiasis in a patient presenting with white discharge in the vaginal canal?

A

Gonorrhea presents with urethritis and PID.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
327
Q

Name the 3 branches of the aortic arch, in order from the heart.

A
  1. R brachiocephalic trunk (branching to R common carotid, R subclav and thyroid ima)
  2. L common carotid
  3. L subclavian
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
328
Q

What is lambert-eaton syndrome?

A

A paraneoplastic syndrome in which antibodies are generated against presynaptic calcium channels at the neuromuscular junction.

Symptoms include proximal muscle weakness, decreased reflexes, sometimes diplopia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
329
Q

What changes do you expect to serum calcium, phosphorus and alkaline phosphatase in the setting of a patient with osteoporosis?

A

All will be normal.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
330
Q

What percentage of RB mutations are spontaneous?

A

55% of cases involve two spontaneous mutations

In the other 40%, kids inherit one allele which is mutated and develop a spontaneous mutation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
331
Q

An individual reports a growing mass exuding a yellow discharge one month post oral surgery. What is the causative organism based on this acid-fast stain?

A

Actinomyces israeli, a branching rod-like gram-positive obligate anaerobe.

Characteristic sulfur granules, negative on acid-fast stain.

Treat with penicillin G

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
332
Q

What is the mechanism of action of sulfonamides?

A

Block bacterial nucleotide synthesis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
333
Q

What is the mechanism of action of penicillin G (IV/IM) or V (oral)?

A

Inhibits transpeptidase cross-linking and prevents cell wall synthesis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
334
Q

What is the mecahism of action of amphotericin B?

A

Binds ergosterol, forms pores in the membrane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
335
Q

What is the mechanism of action of azoles?

A

Inhibits ergosterol synthesis (fungal infections!).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
336
Q

What markers are found on T helper cells?

A

CD4, CD40L, CXCR4/CCR5 (co-receptors for HIV)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
337
Q

CD5 is found on what cells?

A

most T cells (and also CLL cells)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
338
Q

What markers do NK cells have?

A

CD16 and CD56

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
339
Q

What marker is found on cytotoxic T cells?

A

CD8

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
340
Q

What markers are found on B cells?

A

CD19, CD20 and CD21

CD40

MHC II

Ig (binds antigen)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
341
Q

What are these findings suggestive of in the context of fever and new heart murmur? What is the most common causative organism?

A

These are roth spots, osler nodes janeway lesions and nail-bed hemorrhage, suggestive of bacterial endocarditis.

Acute onset tends to be Staph aureus

Subacute is viridans streptococci (tends to be associated with dental work)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
342
Q

What is the classification of vvridans streptococci?

A

Gram-positive Cocci

Catalase-negative

alpha-hemolytic

opthrocin resistant

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
343
Q

identify the brain tumor

A

oligodendroglioma: Fried egg with interspersed “chicken-wire” capillaries

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
344
Q

A sudden swollen, warm exquisitely tender big toe is a classic presentation of…

A

gout

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
345
Q

What is the presentation of neuroleptic malignant syndrome? What is the best management?

A

Fever, muscle rigidity, myoglobinuria, altered mental status.

Start benzodiazepines, then dantrolene (skeletal muscle relaxant) or bromocriptine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
346
Q

If the hip drops to the left (Tredelenburg), which side is weak?

A

The right gluteals; could be due to damage to the superior gluteal nerve (nerve roots L4-S1)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
347
Q

What is this finding on RBC smear called? Which disease process does it suggest?

A

Rouleaux formation, Multiple myeloma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
348
Q

What is the mechanism of action for the antibiotic commonly used to treat C. diff and MRSA?

A

Vancomycin is used for gram-positive infections; it binds D-ala-D-ala and prevents cell wall synthesis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
349
Q

The following lesion appears on a patient with HIV. What is the cause of the lesion and the most common accompanying symptoms?

A

Kaposi sarcoma (a malignant proliferation of epithelial cells caused by HHV-8 infection).

Can be accompanied by mucosal bleeding leading to hematochezia, hematemesis or melena.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
350
Q

What conditions are associated with von Hippel-Lindau syndrome? Which chromosome is it located on?

A

chromosome 3p25
hemangioblastoma of the cerebellum, retinal capillary and spinal cord, polycythemia, renal cell carcinoma and pheochromocytoma.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
351
Q

In a fetus at risk of pre-term birth, what are steroids used for?

A

To increase fetal lung compliance (promotes synsthesis of surfactant by maturation of type II pneumocytes)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
352
Q

What is the presentation of 21-hydroxylase deficiency?

A

Congenital adrenal hyperplasia, salt-wasting hypotension (no aldosterone and cortisol) with shunting towards sex hormones.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
353
Q

What is the cause of the following tumor? In which ages does it present?

A

This is a Wilms tumor, common in young children between 2-4 years old. They arise from neoplastic embryonic renal cells -> abnormal proliferation of metanephric blastema (nephrogenic rests).

Can be associated with WAGR syndrome with WT1 mutation on chromosome 11.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
354
Q

What is WAGR syndrome?

A

Wilms tumor

Aniridia

Genitourinary abnormalities

mental Retardation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
355
Q

What is the indication and mechanism of action of prochlorperazine?

A

It is used as an antipsychotic agent and also potent antiemetic as an adjunct to chemo.

Acts by blocking D2 receptors in the chemotrigger receptor zone, located in the area postrema in the medulla.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
356
Q

How do you calculate sensitivity?

A

TP / (TP + FN)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
357
Q

How do you calculate specificity?

A

TN / (TN + FP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
358
Q

What is the virulence factor that contributes to sepsis in Neisseria meningitidis?

A

Lipooligosaccharide (stimulates inflammatory cytokines similarly to LPS)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
359
Q

HIV encephalopathy occurs due to infection of what cells in the brain?

A

macrophages and microglia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
360
Q

What is the critical period of fetal development for teratogen exposure?

A

weeks 3-8

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
361
Q

What are common manifestations of uncal herniations?

A

Ipsilateral CN III compression (fixed dilated pupil, “down and out” eyeball, ptosis)

Contralateral hemiplagia (or ipsilateral if compression hits the structures on the other side of the brain)

Impaired consciousness.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
362
Q

Identify the thyroid carcinoma. What are the key characteristics?

A

Papillary thyroid carcinoma. Commonly presents with asymptomatic cold nodule after previous radiation exposure.

Large overlapping nuclei with finely dispersed chromatin; often optically clear.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
363
Q

What cells are characteristic of anaplastic thyroid cancer?

A

Large osteoclast-like multinucleated giant cells and biphasic spindle cells amongst sheets of undifferentiated pleomorphic cells.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
364
Q

What is panacinar emphysema?

A

Alpha-1 antitrypsin deficiency leads to chronic and progressive dyspnia and liver failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
365
Q

How does CF affect the gut?

A

accumulation of pancreatic enzymes in the pancreas -> pancreatitis

Nutrient malabsorption due to dessication -> weight loss, potential obstruction

Biliary secretions are impaired -> biliary cirrhosis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
366
Q

Describe the effects of tamoxifen

A

It is a selective estrogen receptor modulator

estrogen antagonist in breast

estrogen agonist in bone (inhibits osteoclasts) and uterus (increases risk of endometrial carcinoma)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
367
Q

What is an important side effect of heparin?

A

heparin induced thrombocytopenia (a type II reaction) due to antibodies against heparin/platelet factor 4 complex.

Occurs with a drop of 50%+ platelets in 3-10 days following treatment. More common with previous exposure to heparin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
368
Q

Which symptoms make a diagnosis of henoch-schônlein purpura more likely vs granulomatosis with polyangiitis?

A

HSP -> arthralgia and abdo pain

GPA -> upper and lower resp findings, nephritic syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
369
Q

What is the mechanism of action of metronidazole?

A

Forms free-radical metabolites that damage bacterial or protozoan DNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
370
Q

Galactorrhea, abdo pain relieved by eating and hypercalcemia raises suspicion for which syndrome?

A

Multiple endocrine neoplasia type 1 (pituitary prolactinoma, zollinger-ellison syndrome caused by gastrinoma, parathyroid neoplasm).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
371
Q

A beta antagonist would have what effect on cAMP?

A

Decreased cAMP (because normally beta receptors are Gs -> increased cAMP).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
372
Q

How would you distinguish between hypercalcemia caused by parathyroid neoplasm and a lytic bone disease (e.g. multiple myeloma)

A

Alkaline phosphatase levels should be elevated in PTH neoplasm

Multiple myeloma is often accompanied by proteinuria (due to excessive antibody production).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
373
Q

What is the clinical presentation of invasive ductal carcinoma?

A

Mass with sharp margins with dimpling on the skin. Biopsy shows small glandular cells with a stellate appearance.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
374
Q

What is the clinical presentation of Paget’s disease.

A

Eczematous patches on nipple.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
375
Q

What chromosomal abnormality is associated with Hirschsprung disease?

A

Down syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
376
Q

What is the motor and sensory distribution of the musculocutaneous nerve? Which nerve roots does it originate from?

A

Motor: coracobrachialis, biceps, brachialis

Sensory: lateral part of the forearm

Roots: C5-C7

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
377
Q

Which cells are involved in acute graph rejection?

A

Activation of cytotoxic T-cells (CD8)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
378
Q

How do you treat achalasia?

A

Use calcium channel blockers e.g. nifedipine or nitroglycerin to have smooth muscle relaxation.

Botulinum toxin can be used as well.

Surgery is another option.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
379
Q

What are the 2 possible diagnoses for the abnormality on blood smear?

What finding would you see on labs?

A

These are spherocytes

Hereditary spherocytosis or autoimmune hemolytic anemia.

Increased mean cell hemoglobin concentration (MCHC)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
380
Q

What is trichotillomania?

A

Compulsive hair-pulling resulting in hair loss. Often precipitated by tension.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
381
Q

What is alopecia areata?

A

An autoimmune hair loss disorder. No inflammation, no scarring, no itching painless hair loss, often accompanied by nail pitting

382
Q

Describe the differences between CIN 1, 2 and 3

A

Cin 1 -> low-grade intraepithelial neoplasia < 1/3 of epithelium

CIN 2 -> between 1/3 and 2/3

CIN 3 -> between 2/3 and full thickness.

Invasion beyond the epithelium = invasive cervical carcinoma

383
Q

A patient presents with frequent resp infections, broductive cough with pus and bloody sputum, rales and ronchi on auscultation. What is the diagnosis?

A

Bronchiectasis (thickening of the bronchial walls due to inflammation/infection)

384
Q

What are these bodies called? What is the diagnosis?

A

Hentz bodies, G6PD deficiency

385
Q

What is the fracture? Which nerve is most likely impacted?

A

Supracondylar fracture of the humerus -> median nerve.

386
Q

Which fracture would typically be associated with a radial nerve injury?

A

Midshaft fracture of humerus, compression of the axilla.

387
Q

Which fracture would present as an ulnar nerve injury?

A

Fracture of the medial epicondyle of the humerus

388
Q

How would you distinguish between a radial, ulnar and median nerve injury?

A

Rardial nerve -> wrist drop, loss of grip strength, loss of sensation over posterior arm and forearm

Ulnar -> loss of wrist flexion, flexion of medial fingers, abduction and adduction of fingers, loss of sensation over little finger and half of ring finger as well as hypothenar eminence.

Median -> loss of grip strength, decreased sensation over thumb and lateral 3 fingers.

389
Q

Which translocation is associated with follicular lymphoma? What are the clinical and histological signs?

A

t(14;18) -> bcl-2

Recapitulates lymph node architecture.

Presents as waxing and waning painless peripheral adenopathy, splenomegaly and B symptoms.

390
Q

Differentiate between somatic symptom disorder and conversion disorder

A

Conversion disorder mimics voluntary motor or sensory system disease, but patients typically have a lack of concern about symptoms

Somatic symptom disorder is significant distress or impairment due to one or more somatic symptoms

391
Q

What is a systemic strategy for improving patient sign-outs, CAUTI and ventilator-associated pneumonia?

A

Implementing a checklist!

392
Q

What are the most common causes of aortic stenosis?

A

< 60y.o, US -> bicuspid aortic valve

Developing countries -> rhematic heart disease (often presents with mitral defects)

393
Q

What is the presentation of a tumor that stains positive for S100 protein at the cerebellopontine angle?

A

This is an acoustic neuroma (a schwannoma).

Presentation: hearing loss, dizziness, and impaired balance.

394
Q

Bilateral acoustic neuroma is pathognomonic for…?

A

Neurofibromatosis type 2.

395
Q

What medication would you use to address torticolis subsequent to haloperidol?

A

Benztropine (an anticholinergic agent).

396
Q

What disorder is associated with type I collagen defect?

A

Osteogenesis imperfecta: blue sclerae, tooth abnormalities, multiple fractures and hearing loss.

397
Q

What disorders is associated with type II collagen defects?

A

Kniest dysplasia (short stature)

Stickler syndrome (hereditary ophalmoarthropathy, deafness)

398
Q

What disorder is associated with type III collagen?

A

Ehlers-Danlos syndrome (EDS), vascular type. Aneurysmal, organ rupture, milder skin/joint issues.

399
Q

Which disorder is associated with type IV collagen?

A

Alport syndrome (X-linked dominant inheritance)

Eye problems, glomerulonephritis, sensorineural deafness.

400
Q

What is metoclopramide used for?

A

A prokinetic agent for GI motility (blocks D2 receptors). Is also useful as an antiemetic (D2 CNS receptors).

Parkinsonian symptoms can result as side-effects.

401
Q

What is bethanechol used for?

A

Gastric prokinetic agent -> cholinergic side-effects.

402
Q

What is scopolamine used for?

A

Anticholinergic used for nausea.

403
Q

What is the most common cause of death for patients >65 years old

A

Heart disease

404
Q

What is the only treatment for familial adenomatous polyposis?

A

Full colonic resection.

405
Q

What are the physiological effects of beta-blockers on the heart?

A

Reduced sympathetic tone -> lower HR

Lower HR -> increased duration of diastole and increased coronary filling.

Decreased contractility, cardiac output, HR, and vasoconstriction.

406
Q

What is the classic presentation of Marfan syndrome?

A

Dislocated lens, tall stature, scoliosis, aortic involvement (aortic regurg)

407
Q

A positive hydrogen breath test with an increased stool osmotic gap in the setting of normal-appearing villi and abdo pain, diarrhea, flatulence would raise suspicion for what condition?

A

Lactose intolerance

408
Q

What does this ECG show?

A

Wolf-Parkinson-White syndrome.

Key findings are short PR, long/wide QRS, upsloping early QRS, commonly presenting with AVRT.

Due to an accessory tract bypassing the AV node

409
Q

This individual has a creatininne of 1 mg/dL. What is the most likely diagnosis?

A

increased PTH

410
Q

A “blowing” holosystolic murmur would suggest what kind of pathology in a 4-year-old?

A

Ventricular septal defect.

411
Q

What is the second-line therapy for high cholesterol?

A

Niacin -> significantly elevated HDL, reduced hepatic triglyceride and VLDL synthesis.

Side effects: flushing.

412
Q

How would you differentiate between von Willebrand disease and hemophilia A and B?

A

vWD typically presents with epistaxis, menorrhagia, prolonged bleeding after procedure (primary hemostasis).

Hemophilia A and B is going to present appropriate hemostasis during procedure but secondary hemorrhage into joints and muscle compartments.

Reduced ristocetin-induced platelet activation is specific and sensitive for vWF

413
Q

What is asherman syndrome?

A

Secondary amenorrhea due to scarring of the endometrial layer of the uterine cavity

414
Q

What is Kallmann syndrome?

A

Congential hypogonadotropic hypogonadism due to failure of migration of GnRH-producing neurons.

415
Q

How would you address a patient that has deficiency of interleukin-12?

A

Treat with interferon-gamma, which supports Th1 differentiation.

416
Q

What is the unhappy triad of knee injury?

A

ACL injury, damage to medial meniscus and MCL (positive McMurray to valgus pressure).

417
Q

What is the anatomic location of a direct inguinal hernia?

A

Medial to the inferior epigastric vessels, lateral to the rectus abdominis and superior to the inguinal ligament

418
Q

What is the anatomical location of an indirect inguinal hernia

A

Lateral to the inferior epigastric artery and superior to the inguinal ligament

419
Q

What is the most common cause of subarachnoid hemorrhage?

A

Ruptured arterial aneurysm.

420
Q

What are the structures labeled A-E? What is their relevance for parkinson disease?

A

A = globus pallidus. Surgical ablation of the internal segment reduces inhibitory tone to the thalamus, improving bradykinesia

B = Putamen

C = Internal capsule (transmission of motor signals from cortex to body)

D = Caudate nucleus

E = Corpus callosum

421
Q

What is the most common cause of cholelithiasis?

A

Increased cholesterol secretion in bile leading to cholesterol stones.

422
Q

How would you distinguish between cholecystitis and biliary colic?

A

Chole -> fever, persistent abdo pain, murphy’s

Biliary colic -> intermittent abdo pain radiating to back, worse after meals.

423
Q

Which malignancies are associated with asbestosis? What distinguishes them?

A

Bronchogenic carcinoma -> multiplicative effect with smoking, presents with hemoptysis

Mesothelioma -> not associated with smoking, presents 30-40y after exposure with pleuritic chest pain and SoB.

424
Q

What is the most common cause of acute MI?

A

Plaque rupture with background atherosclerosis.

425
Q

How would you distinguish between Scurvy and Vitamin K deficiency?

A

Vitamin K deficiency -> bleeding subsequent to broad spectrum antibiotics or in neonates

Vitamin C / Scruvy -> bleeding subsequent to malnutrition, with swollen gums, bruising petichiae, corkscrew hair.

426
Q

What is the inheritance pattern of von Hippel-Lindau disease?

A

Autosomal dominant.

427
Q

What is a sentinel event? What must be done in response?

A

Sentinel event = an unexpected occurance involving death or serious injury

Must do a root cause analysis.

428
Q

What is failure mode and effect analysis?

A

Attempting to identify the most likely or risky points of failure in a system in order to mitigate them.

429
Q

What is the venous drainage of internal and external hemorrhoids?

A

Internal hemorrhoids -> painless, drains to superior rectal vein

External hemorrhoids -> painful, drains to inferior rectal vein to IVC.

430
Q

How does shigella infect the host?

A

Invades M cells in peyer patches.

431
Q

What is a courvoisier sign? Which disease is most likely?

A

Courvoisier = palpable gallbladder.

Pancreatic cancer (often also presents with painless jaundice, new-onset diabetes mellitus as the neoplasm blocks the bile ducts and pancreatic ducts).

432
Q

What is the most likely consequence of an untreated hydratiform mole?

A

Choriocarcinoma

433
Q

How does rabies infect the CNS?

A

Direct infection and retrograde axonal transport.

434
Q

How do you distinguish between legionella pneumonia and tuberculosis?

A

Leogionella -> thrombocytopeneia, elevated creatinine and BUN suggestive of kidney involvement as well as abdo pain.

Tuberculosis -> chronic cough, fever, night sweats and weight loss.

435
Q

What is the first-line treatment of HTN in pregnancy? What must be co-administered with it?

A

Hydralazine

A beta blocker (e.g. labetalol) to counter tachycardia

436
Q

What effects are linked to amiodarone?

A

Hypo/hyperthyroid, pulmonary fibrosis, blue-gray skin deposits, photodermatitis, neurologic effects, constipation, HF, heart block, bradycardia.

437
Q

Differentiate between Wilson disease and hereditary hemochromatosis.

A

Wilson -> copper accumulates in the liver (cirrhosis), brain (parkinson-like, hemibalismus, dementia), cornea (Kayser-Fleischer rings). Caused by a ceruloplasmin mutation.

Hemochromatosis: Bronze diabetes, decreased libido/ED. Micronodular cirrhosis. Caused by AR HFE gene mutation, leading to excessive iron absorption.

438
Q

Differentiate between CF and Kartagener syndrome

A

Kartagener -> situs inversus, no ileus (ciliary dysmotility)

439
Q

In addition to strawberry tongue, what are the other symptoms of Kawasaki disease?

A

High fever, cracked lips, conjunctivitis.

440
Q

What is a dangerous complication that can result from Kawasaki disease?

A

Coronary aneurysm and MI

441
Q

What is tumor lysis syndrome? How is it treated?

A

hyperkalemia, hyperuricemia and hyperphosphatemia with secondary hypercalcemia secondary to chemotherapy.

Treat with allopurinol to reduce uric acid production.

442
Q

What is the mechanism of action of the 1st-line treatment for asthma exacerbation?

A

1st line treatment is a B2 receptor agonist, leading to Gs activation of PKA and block of MLCK.

B2 = 2 lungs

443
Q

How do you treat hereditary spherocytosis?

A

Splenectomy

444
Q

What are the saliient features of this liver biopsy? What is the diagnosis?

A

Hypercellularity, hygh nuclear-to-cytoplasm ratio, pleomorphism. May be accompanied by bruit

Hepatocellular carcinoma.

445
Q

What is a hemangioma?

A

A benign tumor (most common noncancerous liver tumor), liver bruit can be heard, but B syptoms and malignant hepatocytes not found.

446
Q

How does tissue plasminogen activator (tPA) and other clotbusters work?

A

Convert plasminogen to plasmin, leading to cleavage of thrombin and fibrin clots.

447
Q

How does heparin work?

A

Heparin activates antithrombin III, which inactivates Xa and thrombin.

448
Q

How do clopidogrel and ticlodipine work?

A

They inhibit the binding of fibrinogen to platlets, blocking further clot formation.

449
Q

What is I-cell disease? What is the cause?

A

AKA mucolipidosis II or inclusion cell disease. Presents with joint contractures and umbilical/inguinal hernia. Due to deficiency of N-acetylglucosamine-1-phosphotransferase leading to inability to correctly tag enzymes for direction to lysosomes via mannose-6-phosphate attachment.

450
Q

What are the symptoms of the 4 major dopaminergic pathways and their relationship to schizophrenia?

A

Mesocortical -> decreased activity = negative symptoms

Mesolimbic -> increased activity = positive symptoms (hallucination)

Nigostraiatal -> decreased activity = dystonia, tarditive dyskinessia, parkinsonism

Tuberoinfundibular -> decreased activity = increased prolactin and sexual dysfunction.

451
Q

What is the best management for somatic symptom disorder?

A

Continued follow-up with the same provider. Reduces unnecessary testing and fragmentation of care.

452
Q

What are germ tube-negative fungi?

A

Histoplasmosis, blastomycosis, coccidiomycosis with some candidia.

453
Q

What are germ tube-positive fungi?

A

Candida albicans

454
Q

What brain tumors have foamy cells and high vascularity?

A

Hemangioblastoma -> not usually found in the cerebellar midline.

455
Q

Name the brain tumor. What are the characteristic findings?

A

Medulloblastoma: small blue cells around a neuropil (homer-wright rosette). They are the most common cerebellar midline tumor in children and can cause hydrocephalus and present with truncal ataxia and gait disturbances.

456
Q

How do you distinguish between autoimmune hemolytic anemia, MAHA and PNH?

A

Autoimmune hemolytic anemia = direct Coombs test, increased LDH, increased bilirubin, decreased haptoglobin.

MAHA = negative direct Coombs, presents with fatigue anemia and thrombocytopenia. Concomitant small-vessel occlusion pathology.

PNH = negative direct Coombs, morning hematuria.

457
Q

What HLA is associated with T1DM?

A

HLA-DR3

458
Q

What HLAs are assocaiated with hemochromatosis?

A

HLA-A3

459
Q

What HLAs are associated with celiac disease?

A

HLA-DQ2

460
Q

What diseases are associated with HLA-DR2

A

MS, hay fever, SLE, goodpasture syndrome.

461
Q

What is the most common side-effect of ethambutol?

A

Bilateral optiic neuritis.

462
Q

What is the presentation of CREST? What autoantibodies are associated?

A

Calcinosis

Raynaud

Esophageal dysfunction

Sclerodactyly

Telangiectasias,

Caused by anticentromere antibodies.

463
Q

What is the first-line treatment for chemotherapy-associated nausea? How does it work?

A

Odansetron, a 5-HT3 receptor antagonist.

464
Q

How would you diagnose gallstone ileus?

A

Air in the biliary tree, bowel obstruction, cholelithiasis without cholecystitis, bilious vomiting.

Caused by a large gallstone that goes through a fistula between gallbladder and SI and then blocks the ileocecal valve.

465
Q

What are the three blood vessels contained in the umbilical cord?

A

2 umbilic arteries (returning deoxygenated blood from fetus)

1 umbilical vein carrying oxygenated blood from the placenta

466
Q

What is suggestive of uremic platelet dysfunction? What is the impact on PT PTT and platelets?

A

Prolonged mucosal bleeding and bruising, elevated blood urea nitrogen and chronic kidney disease are hallmarks of uremic platelet dysfunction.

PT, PTT, and platelets will be normal as nitric oxide interferes with platelet adhesion and aggregation as well as platelet endothelium interaction.

467
Q

What is the mechanism by which bacillus anthracis causes cell necrosis?

A

Anthrax has edema factor and lethal factor. EF increases cAMP, LF removes the n-term from MAPKK.

468
Q

Which organisms are associated with painless sores?

A

Syphilis and anthrax.

469
Q

What is the mechanism of cholera toxin?

A

Constitutional activation of the GS subunit leading to increased cAMP and increase chloride secretion into gut following with water.

470
Q

Which virus is associated with increased risk of Hodgkin’s lymphoma?

A

EBV

471
Q

What medication can be given in an MI to relieve pain? What is the mechanism?

A

Nitroglycerin for angina; produces venous dilation and decreased preload, ultimately reducing myocardial O2 concentration.

472
Q

Which bacteria most commonly causes urinary tract infections in individuals with a Foley catheter, specifically with the presentation of aortic valve endocarditis?

A

Enterococcus faecalis (gram +ve, negative nitrite on urinalysis)

473
Q

What is the mechanism of action of Spironolactone?

A

It is a competitive inhibitor of aldosterone binding.

474
Q

Which 2 tumor markers are associated with a presentation of constitutional symptoms, jaundice and hepatomegaly along with elevated amylase, lipase, and alkaline phosphatase?

A

Pancreatic cancer, specifically CA19-9 and cardioembryonic antigen (CEA)

475
Q

What does this x-ray show? What additional findings are associated with this condition?

A

Congenital diaphragmatic hernia.

Typical findings on exam include scaphoid abdomen and barrel chest

Also presents with pulmonary hypoplasia and pulmonary hypertension (pulmonary artery pressure >22mmHg)

476
Q

What is hantavirus cardiopulmonary syndrome? What would you see on exam, CXR and investigations? What is the natural reservoir for the causative organism?

A

O/e: Fever, myalgia, cough, headache, N/V

CXR: Pulmonary edema (bilateral lung infiltrates and pleural effusions)

Labs: Leukocytosis, thrombocytopenia, elevated liver enzymes

Hantavirus tranmission occurs via rodent contact (e.g. deer mice feces).

477
Q

What is the window to give tPA for stroke?

A

3.5-4hrs after first onset of symptoms

478
Q

How do you reverse tPA? How does this agent work?

A

Aminocaproic acid (blocks conversion of plasminogen to plasmin).

479
Q

What cardiac tumor is associated with tuberrous sclerosis?

A

Rhabdomyoma (typically on an atrial or ventricular wall).

480
Q

Which GPCR act via the Gq pathway (phospholipase C -> PKC -> smooth muscle contraction)?

A

HAVe 1

M1 & M3

481
Q

Which GPCRs act via the Gs pathway (Stimulation of adenylate cyclase)?

A

all the Bs (B1, B2 and B3), D1, H2, V2

482
Q

Which GPCR act via the Gi pathway (inhibition of adenylate cyclase)

A

2 MAD

483
Q

Identify the atria and ventricles on this echo

A

A -> RV

B -> LV

C -> LA

D -> RA

E-> cardiac apex

484
Q

Name other thiazide diuretics than hydrochlorothiazide

A

Chlorthalidone, indapamide, metolazone

485
Q

What is the classic presentation of somatostatinoma? Which pancreatic cells normally produce this hormone?

A

Somatostatinoma -> tumor secreting somatostatin. Classic presentation is steatorrhea, diabetes melllitus, gallstones. Labs will show decreased amylase, lipase, insulin, pepsio.ngen and glucagon.

Somatostatin is normally secreted by D cells in the pancreas.

486
Q

What is the first step in management of a patient with obstructive sleep apnea?

A

Polysomnography.

487
Q

What is a common complication of ulcerative colitis?

A

Primary sclerosing cholangitis (note that most folks with PSC develop UC, but not necessarily the other way around)

488
Q

Describe rhabdomyolysis. What drugs are associated with it?

A

Classic triad: myalgias, generalized weakness, myoglobinuria -> ATN.

Statin-induced

489
Q

What is the diagnosis in this pre-term neonate with dyspnea and cyanosis? How would you differentiate between the common syndromes which lead to neonatal respiratory distress?

A

Atelectasis with air bronchograms and low lung volumes = NRDS

TTN would present with pulmonary edema with increased lung volumes and pleural effusion.

490
Q

What are characteristic symptoms and ECG presentation for hyperkalemia?

A

Ascending flaccid muscle paralysis.

ECG shows peaked T waves in a wide QRS with sinus bradycardia.

491
Q

What is the ACLS algorithm for the treatment of ventricular fibrillation?

A
  1. Defibrillation
  2. Epinephrine
  3. Amiodarone
492
Q

What is the first-line treatment for community acquired pneumonia?

A

Doxycyclin or a macrolide (erythromycin, clarithromycin, azithromycin).

493
Q

Which antibiotics can interact with statins?

A

Macrolides (erythromycin, clarithromycin, azithromycin) inhibit cytochrome P450 which increases statin concentrations.

494
Q

What is monoclonal gammopathy of undetermined significance? How is it managed?

A

Elevated serum protein with <3g/dL of M protein in an otherwise asymptomatic individual.

Management is follow-up retesting in 6 mos to rule out progression to multiple myeloma.

495
Q

How would you landmark the placement of a central line within the internal jugular vein

A

Lateral to the common carotid artery

496
Q

What symptoms are concerning for Zollinger-Ellison syndrome?

A

Gastric ulcers that are refractory to PPIs and distal to the duodenal bulb = elevated gastrin, due to hypersecretion secondary to neoplasm.

497
Q

What hematologic findings occur in the context of COPD?

A

Hypoxemia -> EPO release -> erythrocytosis (polycythemia)

498
Q

What drugs can intefere with absorption of fluoroquinolones?

A

Calcium carbonate (in general, polyvalent cations including Ca2+, Mg2+ or Fe2+)

499
Q

Name the arterial derivatives of the aortic arches (1-4, 6)

A
  1. maxillary artery
  2. stapedial and hyoid
  3. common carotid and proximal internal carotid
  4. L -> aortic arch R -> R subclavian
  5. Proximal pulmonary and ductus arteriosus.
500
Q

What pathology is suggested by this murmur?

A

Mitral regurgitation

501
Q

What is the best treatment for a child who has a positive cellophane tape test and nighttime perianal itching?

A

Albendazole, mebendazole or pyrantel pamoate (contraindicated in pregnancy) for the treatment of pinworm.

Must treat the family & counsel washing all the bed linens.

502
Q

What combination of drugs is used in highly active antiretroviral therapy for HIV?

A

Dolutegravir, tenofovir and emtricabine

503
Q

What is ganciclovir used for?

A

Treatment of cytomegalovirus and other herpes viruses.

504
Q

How would you differentiate between chronic hepatitis B and hepatitis C infection?

A

Hepatitis B tends to present with membranous glomerulopathy and arthralgias.

505
Q

What is the first-line treatment for chronic hepatitis B infection?

A

Lifelong treatment with tenofovir.

Side effects can include renal insufficiency and decreased bone density.

506
Q

What is a typical regimen for chronic hepatitis C with accompanying renal disease?

A

Glecaprevir and pibrentasvir

507
Q

What are the characteristics of the most common causative organism for bacterial pharyngitis?

What are the autoimmune complications which may follow infection?

A

Streptococcus pyogenes is a gram-positive, beta-hemolytic coccus growing in chains. It produces M protein which inhibits phagocytosis and mimics human cellular protein epitotpes.

Autoimmune sequelae include rheumatic fever and glomerulonephritis.

508
Q

Development of an air embolism shortly after removal of a central venous catheter represents what kind of medical event?

A

A “never event” or serious reportable event.

509
Q

What kinds of kidney stones are produced in patients with Crohn’s?

A

Calcium oxalate stones (due to increased lipids in gut complexing with calcium, causing an oxalate imbalance).

510
Q

What is the formula to calculate clearance of a drug?

A
511
Q

Name the type IV hypersensitivity reactions

A

T-cell mediated: TB tests, contact dermatitis (touch), erythema nodosum (TB & more), hashimoto Thyroiditis and MS.

512
Q

How are slow waves in the GI tract generated?

A

They are caused by the interstitial cells of Cajal, independent of stimuli. They are the basal rhythm of the gut and are different for each organ.

513
Q

What is the eventual consequence of all progressive CKD? What would you expect to see on labs?

A

Secondary hyperparathyroidism: hypocalcemia, hyperphosphatemia, high PTH, and high alkaline phosphatase.

514
Q

What is a common kidney sequellae of rhabdomyolysis?

A

Acute tubular necrosis

515
Q

What is the diagnosis? What is the cause of this disease? What other findings would you expect?

A

Niemann-Pick
This cherry-red spot would be accompanied by hepatosplenomegaly, neurodegeneration and foamy macrophages with lots of lipid.

This is caused by a sphingomyelinase deficiency (problem converting sphingomyelin to ceramide)

516
Q

What is the characteristic presentation of Crohn’s disease? What type of inflammation is associated?

A

Abdo pain, diarrhea, fatigue, weight loss, apthrous ulcers in the mouth with fecal occult blood.

Transmural inflammation (vs mucosal/submucosal in UC) is characteristic.

517
Q

What is the mechanism for acute respiratory distress syndrome? How it diagnosed?

A

Mechanism: cytokine release (IL-1) stimulates increased cap permeability leading to loss of surfactant, bilateral consolidations, resp failure and PaO2/FiO2 < 300.

518
Q

What is the presentation of 17a-hydroxylase deficiency?

A

Inability to produce glucocorticoids and androgens -> high ACTH and high BP, high mineralocorticoids (but low RAAS activation).

519
Q

Which hormone is elevated in Klinefelter syndrome?

A

FSH and LH, due to low testosterone and inhibin subsequent to primary testicular failure.

520
Q

What is the classic presentation and the largest risk factor for Buerger disease?

A

Decreased distal pulses, dry gangrene, digit ulceration (mimic of PAD).

Buerger disease typically affects smokers < 40s

521
Q

How is premature ovarian failure diagnosed and characterized? What are the common causes?

A

Symptoms of menopause < 40, including anovulatory cycles.

Idiopathic, chemo, radiation, some genetic disorders.

522
Q

What is the cause of this image?

A

Pyruvate kinase deficiency (AR), resulting in splenomegaly and anemia

523
Q

What is the cause and presentation of primary dysmenorrhea?

A

Diagnosis of exclusion, typically < 30 yo

Crampy lower abdominal pain during menses without a clear explanation, though to be due to increased prostaglandin release. Treatment is OCP +/- NSAID.

524
Q

What is the leading cause of death in patients with a ruptured proximal aortic dissection?

A

Cardiac tamponade.

525
Q

What is the first-line treatment for pseudomonal infections?

A

Inhaled tobramycin

526
Q

A pregnant patient experiencing fetal distress, cramping, a hypertonic uterus and vaginal bleeding without trauma suggests what condition? What are risk factors for it? What are the complications?

A

Placental abruption

Risk factors include smoking, cocaine use, trauma, hypertension and preeclampsia

Complications include fetal death, maternal shock and DIC

527
Q

What is D-dimer? When might it be elevated?

A

D-dimer is a breakdown product from fimbrin, and is elevated in the setting of thrombosis.

528
Q

What are fibrin split products?

A

They are created and measured when plasmin degrades blood clots.

529
Q

Describe the stages of tissue damage and repair post MI

A
  1. Wavy fibers < 12h post MI
  2. Neutrophilic infiltration and coagulative necrosis 1-3 days
  3. Macrophages 3+ days
  4. Granulation tissue 1 week
  5. Collagen deposition 2-3 weeks
530
Q

What is pulmonary capillary wedge pressure? How does it usually relate to central venous pressure?

A

It is an estimate of left atrial pressure, and usually is correlated with central venous pressure. It can be used to ascertain the degree of mitral valve stenosis.

531
Q

What is fitz-hugh-curtis syndrome?

A

RUQ pain in PID due to liver capsule involvement with violin-string attachmentss.

532
Q

What is the diagnosis based on CT? What findings do you expect on CBC?

A

Pulmonary fibrosis (idiopathic), a restrictive lung disease.

Expect to see elevated hemoglobin and hematocrit due to compensation.

533
Q

What lipid-lowering drug is associated with cholesterol stones?

A

Gemfibrozil (and other fibrates)

534
Q

How is MS diagnosed? What are common presentations?

A

Must have 2 separate attacks with 2 different lesions.

Presentation: sensory/motor deficits often in extremities, optic neuritis, cerebellar abnormalities.

535
Q

What are the characteristics of the infective organism that should be suspected in a transplant patient who presents with fever, SOB, non-productive cough, N/V and tachypnea?

A

Cytomegalovirus (CMV), it is an enveloped, double-stratended linear DNA virus latent in mononuclear cells.

536
Q

Which enzyme is deficient in hereditary fructose intolerance? How do these patients usually present?

A

Aldolase B: presents with a low glucose level + lethargy, tachypnea, tremors, hypothermia and diaphoresis + emesis post fruit / fruit-juice introduction.

537
Q

What is indicated in a patient with PE subsequent to DVT? What is the mechanism of action?

A

Low molecular weight heparin, which activates antithrombin which in turn inhibits Xa

538
Q

What is porphyria cutanea tarda?

A

Caused by defects in uroporphyrinogen decarboxylase (a cytoplasmic enzyme).

Presentation is tea-colored urine + blistering skin lesions on sun exposure.

539
Q

What is a cystic hygroma?

A

Abnormal growth on a baby’s neck/head caused by errors in fetal develpoment of lymphatic tissue, one or many fluid-filled cysts that tends to grow over time.. Often associated with other congenital abnormalities.

540
Q

What is the cause of the wavy bands that characterize the first stage of tissue change immediately following an MI?

A

Calcium influx due to reperfusion leading to “hypercontraction”

541
Q

What is the mechanism of action of warfarin?

A

It inhibits the extrinsic clotting pathway (factor VII).

542
Q

What is the most common cause of bronchiolitis? What are the characteristic proteins and their effects?

A

RSV (single stranded, negative-sense paramyxovirus).

G protein attaches it to the epithelium

F protein fuses the virus to the resp epi and causes nearby membranes to merge.

543
Q

How can you diagnose the flu?

What are the key viral characteristics?

How does influenza mutate in seasonal outbreaks vs pandemic-level infections?

A

Flu can be diagnosed by fever, malaise, cough and muscle aches with no nasal drainage along with a positive rapid antigen test.

Influenza is an enveloped, negative-sense, ssRNA genome with 8 segments.

Seasonal outbreaks = point mutations; pandemic = genetic reassortment

544
Q

What is the presentation of renal papillary necrosis? What are the primary causes?

A

Presentation: gross hematuria, proteinuria and flank pain

causes SAAD

Sickle cell

Acute pyelonephritis

Analgesics (NSAIDS)

Diabetes mellitus

545
Q

What is the cause and presentation of diffuse esophageal spasm? How is it diagnosed?

A

Carused by loss of inhibitory innervation in the myenteric plexus resulting in periodic, uncoordinated non-peristaltic contractions. Dysphagia and substernal chest pain can result and it may be diagnosed by a corkscrew pattern on barium swallow.

546
Q

What is the cause of these lesions?

A

Warfarin-induced skin necrosis, especially in patients with a protein C or S deficiency. Thrombosis of the skin results when warfarin depletes C and S first, leading to hypercoagulation.

547
Q

What are the causes of dilated cardiomyopathy? How do you diagnose it?

A

CHF -> elevated BNP and an S3.

Causes include: alcohol/cocaine, pregnancy, genetics, hemochromatosis, doxorubicin, coxsackie virus B and Chagas disease.

548
Q

What is the specific epitope of the autoantibodies in goodpasture syndrome?

A

a3 chain of type IV collagen in the glomerular basement membrane (leads to nephritic syndrome, alveolar hemorrhage and hemoptysis).

549
Q

Assuming full immunization and appropreiate PEP, what is the most likely disease to contract in a needlestick injury?

A

Hepatits C

550
Q

How would you distinguish between bronchial asthma and chronic bronchitis?

A

Chronic bronchitis will present with a consistent productive cough.

551
Q

What is the diagnosis? What are the relevant features?

A

Bronchial asthma: obstruction of the lumen with mucoid exudate, goblet cell metaplasia and smooth muscle hypertrophy.

552
Q

When adding an inhaled corticosteroid for asthma management, what should you counsel? Why?

A

Rinse out the mouth after taking the puffer to reduce the risk of oral thrush.

553
Q

What is a differential for a scrapable oral plaque?

A
  1. . superficial burn
  2. candidiasis
  3. pseudomembranous oral ulcers e.g. aphthous, erythema multiforme etc.
  4. morsicatio (chronic biting of cheek, lips or tongue)
554
Q

What is budesonide indicated for?

A

It is a corticosteroid used for Crohn’s, UC and allergic rhinitis.

555
Q

What commonly used steroid requires bioactivation?

A

Prednisone (must be reduced to prednisolone)

556
Q

What is the differential for a spike in the gamma region on serum protein electrophoresis?

A

Amyloidosis, chronic infections, CLL, Hodgkin’s, malignant lymphoma, multiple myeloma, rheumatoid and other collagen diseases, Waldenstrom’s macroglobulinemia, cirrhosis, or monoclonal gammopathy of undetermined significance.

557
Q

What is the classic presentation of CLL?

A

Immune dysfunction, (either ITP or pure red cell aplasia) + lymphadenopathy and hepatosplenomegaly.

558
Q

How would you distinguish between HCC caused by hepatitis B vs hepatitis C?

A

Hep B: can be inherited from parents, tends to occur in younger adults especially in Asia, HCC caused by integration of the viral genome

Hep C: transmitted through needle sharing or drug use, generally presents with HCC later in life due to chronic cirrhosis (malignant conversion)

559
Q

Which features of a colonic polyp suggest the greatest potential for malignancy?

A

Increased size and greater surface area (so villous > tubular)

560
Q

What is the difference between primary biliary cholangitis and primary sclerosing cholangitis?

A

Primary biliary cholangitis affects the smaller bile ducts and typically presents in middle-aged women. It may lead to cirrhosis and destruction of intrahepatic ducts.

Primary sclerosing cholangitis is a common UC complication and presents with periportal fibrosis and stenosis of hepatic bile ducts.

561
Q

How would you distinguish between a patient taking furosemide and hydrochlorothiazide on urinalysis?

A

Both will increase urine sodium chloride and potassium, however HCTZ will lower urine Ca2+ whereas furosamide would increase Ca2+ in the urine. Hyperuricemia and hyperglycemia are also unique to thiazide diuretics.

562
Q

How do you treat euvolemic hyponatremia (e.g. SIADH)?

A

Begin with water restriction to increase plasma sodium.

If symptomatic, use 3% saline or normal saline + furosemide.

563
Q

What are the key findings which are suggestive of AML?

A

Older (age>60), microangiopathic hemolytic anemia, leukopenia, thrombocytopenia, ++myeloblasts (>20%) with multiple auer rods on smear.

564
Q

What is a normal anion gap? What is the differential for an elevated anion gap metabolic acidosis?

A

Normal is <3x serum albumin or < 12 mmol/L

Elevated anion gap could be MUDPILES + CAT

Methanol

Uremia

DKA

Paraldehyde

Iron or Isonazid

Lactic acidosis

Ethanol or Ethylene glycol

Salicylate (ASA, Asprin)

CO

Aminoglycosides

Theophylline

565
Q

What are the side effects of gastric motility agents e.g. metoclopramide?

A

Extrapyramidal symptoms: tremor, dystonia and involuntary movements.

566
Q

How does the heart muscle remodel in response to untreated hypertension?

A

Increased systemic pressure -> L ventricular hypertrophy (additional sarcomeres added in parallel) -> L-sided HF -> R-sided HF sucbsequent to increased pulmonary pressure.

567
Q

What are some diagnostic criteria for TB? What is its virulence factor?

A

Fever, night sweats, productive cough with streaky blood, dyspnea and positive acid-fast stain in sputum.

Cord factor activates macrophages -> TNF-alpha release -> caseating granulomas. Sulfatides inhibits phagolnysosomal fusion.

568
Q

How do you grow TB?

A

Lowenstein-Jensen agar

569
Q

Cavitary lung masses and sarcoidosis can become infected by what organism? What would you expect to see on microscopy? What is the treatment?

A

Aspergillus fumigatus, a mold with septate hyphae branching at 45-degree angles.

Treatment is surgical removal.

570
Q

What condition is associtaed with a t(15;17)?

A

Acute promyelocytic leukemia

(rapid onset fatigue, splenomegaly and bleeding)

571
Q

A colonoscopy reveals yellow-white plaques lining the colon. What is the infective organism? What is the gold-standard test for it?

A

C. difficile pseudomembranous plaques (chronic watery diarrhea and crampy ambdo pain).

Gold standard is toxin assay for A and B toxin.

572
Q

What do you see on this blood smear?

A

Microcytic, hypochromic anemia (most likely iron deficiency).

573
Q

What do you see in this blood smear?

A

Cold agglutinin disease with clumping of RBCs

Associated with blue fingers and toes (painful), previous infection of Mycoplasma pneumoniae or EBV.

574
Q

What are the causes of non-anion gap acidosis?

A

HARDASS

Hyperalimentation

Addison disease

Renal tubular acidosis

Diarrhea (most commonly)

Acetazolamide

Spironolactone

Saline infusion

575
Q

What is the most likely diagnosis based on this picture of a 64yo F

A

Osteoarthritis

576
Q

Gout and pseudogout affect which joints?

A

Large joints e.g. knee.

577
Q

What is Job syndrome?

A

Failure of helper T lymphocytes to make INF-gamma

FATED

Facies (coarse)

Abcesses (without inflammation/erythema)

retained primary teeth

increased IgE

Dermatologic problems e.g. atopic dermatitis

578
Q

Can you use furosemide in a patient with T2DM with pulmonary edema subsequent to CHF?

A

Yes!

579
Q

What is von Recklinghausen’s disease?

A

aka osteitis fibrosa cystica, due to untreated hyperparathyroidism.

Cystic lesions, hypercalcemia, elevated ALP and hypophosphatemia

580
Q

How does alcohol intoxication affect the NADH to NAD+ ratio? How does this change impact glucose levels?

A

Oxidization to acetaldehyde and subsequently acetate increases NADH/NAD+.

High NADH results in pyruvate -> lactate (acidosis) + stops gluconeogenesis in the liver.

581
Q

What does this bone biopsy show?

The infective organism is a gram-negative oxidase-positive rod. What is it?

A

Osteomyelitis

Pseudomonas

Often introduced by IVDU

582
Q

What is the classification of N gonorrheae?

A

Gram-negative diplococci

583
Q

A boy presents with fever, rash, bone swelling and the following skin biopsy.

What is the diagonsis? What would you see on EM?

A

Langerhans cell histiocytosis caused by infiltration of myeloid-progenitor derived cells, more common in boys.

EM shows birbeck granules (striated, rod-like outpouchings)

584
Q

What are associated complications of autosomal dominant polycystic kidney disease (ADPKD)?

A

Berry aneurysms of the circle of Willis, aortic root aneurysm, diverticulosis, mitral valve prolapse.

585
Q

How does ADPKD present?

A

Hematuria (sometimes the only presenting symptom), flank pain, HTN, uTI and progressive renal failure

586
Q

What does a 40% HbS indicate?

A

40% abnormal hemoglobin, suggestive of sickle cell trait (ie heterozygote) which will likely be otherwise silent.

587
Q

What is the embryonal origin of pheochromocytoma?

A

Neural crest cells.

588
Q

Low tryptophan can lead to what vitamin deficincy? How would this present?

A

B3 (niacin) = pellagra

Glossitis

3D: Diarrhea, Dementia, Dermatitis (and Death)

589
Q

How does restrictive lung disease present on PFT?

A

Decreased TLC, FRC, RV, FVC and FEV1

Normal or increased FEV1/FVC

590
Q

Name the organism on this acid fast stain

What is the appropriate antibiotic?

A

Nocardia (gram positve, weakly acid-fast, long branching filaments). Opportunistic (think immunocompromised)

Sulfonamides (TMP-SMX) preferred.

591
Q

What is the mechanism of action of sulfonamides?

A

blocks nucleotide synthesis by inhibiting dyhydropteroate synthase.

592
Q

What is the pathology on this ECG?

What are the inherited causes of this pathology?

A

Long QT interval (>2 large boxes on ECG)

Jervell and Lange-Nielsen syndrome (autosomal recessive KCNQ1 or KCNE1 mutation): bilateral sensorineural hearing loss + defective voltage-gated K+ channels.

Romano-Ward (autosomal dominant K+ and Na+ channel defect) does not have hearing loss.

593
Q

Which hormones share an identical alpha-subunit to bHCG?

A

TSH, LH and FSH

594
Q

What is a conduction aphasia? Which area of the brain is affected?

A

Conduction aphasia = unable to repeat specific words or phrases due to a lesion in the arcuate faciculus (which connects broca and wernicke areas)

595
Q

Differentiate between avoidant and schizoid personality disorders?

A

Avoidant = social inhibition, feeling inadequate, hypersensitive to negative evaluation

Schizoid = voluntary social withdrawal, indifferent to human interaction.

596
Q

Which cells are activated by cytokines and growth factors to form the fibrous cap overlying the atheroma?

A

Vascular smooth muscle cells

597
Q

Which cells secrete gastrin? What does it do?

A

G cells secrete gastrin, which normally induces parietal cells in the stomach to secrete acid.

Zollinger-ellison = pancreatic gastrinoma), presents with refractory PUD

598
Q

How does desquamative interstitial pneumonia typically present? What cells end up filling the alveolI?

A

Gradual shortness of breath + dry cough with hypoxemia in a middle-aged smoker.

Increased dead space and Decreased TLC

On CT, you would see diffuse ground glass opacity with cystic changes.

Alvioli are filled with pigment-laden macrophages (NOT epithelium)

599
Q

What are the signs of FASD? When should you suspect moms of having alcohol consumption?

A

Small eyes, narrow droopy eyelids, small palpebral fissures, smooth philtrum, verminion border on thin upper lip

Also presents with limb dislocations, intellectual disability, heart defects.

Consider liver stigmata and signs of chronic alcohol use e.g. esophageal varices.

600
Q

How would you distinguish between frontal lobe and amygdala lesions?

A

Both present with disinhibition and impaired judgement, but amygdala lesion presents with memory problems.

601
Q

Which conditions are associated with the following lung histology:

Alveolar fluid and hyaline membranes

Infiltration of eosinophils and CD4+ cells

Infiltratration of macrophages and CD8+ cells

A
  1. Adult respiratory distress syndrome
  2. Asthma
  3. Chronic bronchitis
602
Q

What are the diagnostic criteria for chronic bronchitis?

A

Productive cough at least 3 mos/year for 2 years. Obstructive pattern on Pft; FEV1:FVC < 0.7

603
Q

What is the classification of the most common viral causes of meningitis?

A

Enteroviruses - nonenveloped SS linear +RNA

in neonates, children 6+ and adults to age 60 - HSV - enveloped dsDNA with glycoprotein

604
Q

What is the systemic antifungal recommended for tinea corporis? What is its mechanism of action?

A

Griseofulvin

Disrupts microtubules (alpha/beta tubulin dimer).

Disulfiram-like reaction when mixed with alcohol.

605
Q

How do you calculate the filtration fraction from GFR and renal blood flow?

A

FF = GFR / renal plasma flow

Renal plasma flow = renal blood flow * (1-hematocrit)

substited: FF = GFR / (RBF * (1-hematocrit))

606
Q

What is Meigs syndrome? What is the classic triad? What would you see on biopsy? What do these tumours secrete

A

An ovarian fibroma which presents with abdo fullness, ascites, and pleural effusion.

On biopsy: spindle cells and collagen.

No sex hormone secretion.

607
Q

What pathology is indicated when an ECG shows occasional premature ventricular contractions?

A

No underlying pathology.

608
Q

What drugs should be used to treat Addison disease?

A

Dexamethasone (glucocorticoid) + Fludrocortisone (mineralocorticoid)

609
Q

What TB drug has a classic side effect of turning body fluids orange or red? What is its mechanism of action?

A

Rifampin, blocks RNA synthesis via blockage of DNA-dependent RNA polymerase.

610
Q

How would damage to the lateral cords of the brachial plexus present?

A

Lateral: -> musculocutaneuous nerve and median nerve, lateral forearm sensory loss, weakness to elbow flexion and supination, wrist flexion and extension of lateral digits + sensory loss over the thenar eminannce and both sides of the lateral 3 digits.

611
Q

How would damage to the posterior cord present?

A

Posterior -> Axillary and medial nerves; inability to abduct the shoulder and elbow/ wrist / and MCP extension

612
Q

How would damage to the medial cord of the brachial plexus present?

A

Medial -> median + ulnar nerve: weakness of wrist flexion but varies, flexion of medial fingers, abduction/adduction of digits., sensory loss over the medial 1.5 fingers and the hypothenar eminence

613
Q

What is the defective enzyme and the clinical presentation of I cell disease?

A

Defect in N-acetylglucosaminyl-1-phosphotranspherase (makes mannose-6-phos to target proteins to lysosomes)

Clinically presents as skeletal abnormalities, coarse facial features, corneal clouding + psychomotor retardation.

614
Q

What is the arrow pointing to? What disease process could result in this slide?

A

Mallory bodies: eosinophilic inclusions in cytoplasm of necrotic hepatocyteso commonly found in alcoholic hepatitis.

615
Q

Which thumb muscle is innervated by the ulnar nerve?

A

Adductor pollicis

616
Q

What are councilman bodies?

A

Eosinophilic globules due to apoptosis of individual hepatocytes, can occur with yellow fever.

617
Q

What is the causative organism and treatment for a small painless ulcer on the genitals which proceeds to swollen, ulcerated inguinal lymph nodes 4-6 weeks later?

A

Chlamydia trachomatis type L1-3

Treat wyth doxycycline

618
Q

What is shown on this ECG? What drug can cause this effect?

A

Mobitz II heart block (dropped beats with no PR lengthening)

Can be caused by bupivicaine

619
Q

What is the mechanism by which an antibiotic potentiates warfarin’s effect on PT and increases PTT?

A

Via loss of gut bacteria leading to poor absorption of vitamin K.

620
Q

How does chagas disease spread? How does it present?

A

Chagas disease is caused by the intracellular protozoan Trypanosoma cruzi. Spread by reduviid bugs. Presents with myocarditis and dysmotility of hollow organs.

621
Q

What syndrome is associated with endocardial cushon defects in a newborn? What might you see on triple screen prenatally?

A

Down syndrome; low AFP, high BhCG, low estriol.

622
Q

What drugs produce disulfiram-like reactions with alcohol?

A

Sorry Pals, Can’t Go Mingle

Sulfonylureas (tolbutamide)

Procarbazine

Cephalosporins (cefamandole and cefaperazone)

Griseofulvin

Metronidazole

623
Q

How does a cleft lip happen?

A

Failure of the maxilary + medial nasal prominences (philtrum + upper lip to lateral border of nose) or lateral nasal prominences (gap between midphase and lateral nose) to fuse.

624
Q

What is the mechanism of inheritance of chronic granulomatous disease?

A

X-linked recessive

May present in girls via skewed x-inactivation.

625
Q

When a question appears to give you extraneous information that could be “explained away” as not part of the diagnosis, what should you do?

A

Look for one diagnosis that explains even the “apparently extraneous” symptoms.

626
Q

Where in the brain does glioblastoma multiforme present?

A

The cerebrum, never in the cerebellum

627
Q

When multiple masses are found on imaging, what should you be thinking of?

A

Metastasis, less likely to be a primary tumor from that organ.

628
Q

What is the difference between a slip and a lapse?

A

A slip is an error of attention, e.g. due to high stress. A lapse is an error in memory, i.e. forgetting to do something.

629
Q

What is the difference between acting out, displacement, projection and reaction formation?

A

Acting out: using actions to cope with stressors or emotional conflict rather than addressing thoughts and emotions.

Displacement: transferring or attributing feelings to a neutral person or object

Projection: misattributing internal impulses to an external source

Reaction formation: a “warded-off” idea or feeling is replaced by the opposite (like denial on steroids)

630
Q

This person presents with low-voltage QRS complexes, an ejection fraction of 55%, crackles at lung bases and lower-extremity edema. Based on these symptoms and cardiac biopsy below, what is the diaglosis? What is the etiology?

A

Amyloidosis

Primary due to Ig light-chain deposition from bone marrow antibody production or secondary due to chronic inflamation.

Produces restrictive cardiomyopathy (normal ejection fraction)

631
Q

What are the major side effects of doxycycline?

A

Photosensitivity, GI distress, and teeth discolouration (in children < 8)

632
Q

What is the deficient enzyme, inheritance and characteristic presentation of lesch-nyhan syndrome?

A

HGPRT (hypoxanthine-guanine phosphoribosyltransferase), XR

Hyperuricemia (orange crystals in diaper)

Gout

Pissed-off (self-mutilation, aggression)

Retardation

dysTonia

633
Q

What conditions are associated with target cells?

A

liver disease, iron deficiency, thalassemias and postsplenectomy.

634
Q

When does post-streptococcal glomerulonephritis usually present? What is the characteristic kidney finding?

A

10-14 days post-infection, usually in children. Hematuria / nephritic syndrome

635
Q

Which types of E. Coli are associated with bloody diarrhea? Traveller’s diarrhea?

A

Bloody diarrhea: Enterohemorrhagic (EHEC e.g. O157:H7) and enteroinvasive (e.g. O124)

Non-blody: enterotoxigenic (ETEC)

636
Q

What is first-line pharmacotherapy for smoking cession? What is the mechanism of action?

A

Bupropion (norepinephrine + dopamine reuptake inhibitor)

varenicline (nicotine receptor partial agonist)

637
Q

What medication is given that acts centrally for HTN? What is the mechanism of action?

A

Clonidine, an a2-adrenergic agonist lowers sympathetic tone from CNS, thereby lowering blood pressure. Pts must be compliant with medication. bc missed doses can cause spikes in BP>

638
Q

What is fulminant hepatitis?

A

Very rapid deterioration due to massive necrosis of the liver (can be due to viral hepatitis, drug-induced) leading to liver failure, hepatorenal syndrome, DIC and portosystemic encephalopathy progressive to coma and cerebral edema.

639
Q

What is insubordination?

A

Defiance of authority or refusal to obey orders.

640
Q

How would pulmonary capilary wedge pressure change in the setting of septic shock?

A

Initially normal, then decreasing as increased permeability of the lung endothelium leads to fluid loss.

641
Q

What organism causes bloody diarrhea more often than Salmonella and Shigella?

A

Campylobacter jejuni

642
Q

What are the signs of antimuscarinic toxicity? What is the treatment?

A

Fever, rapid pulse, dry mouth, dry flushed skin, cycloplegia, constipation and disorientation

Treat with physostigmine (anticholinesterase inhibitor)

643
Q

Describe the mechanism of action of cephalosporins.

A

Inhibits cell wall synthesis by inhibiting transpeptidases (which cross-link peptidoglycans)

644
Q

What are the risk factors for pancreatic adenocarcinoma? What sign should raise your index of suspicion for this cancer?

A

Smoking, age (65-75), history of chronic pancreatitis, some hereditary syndromes.

Courvoisier sign: a palpable, nontender gallbladder (caused by pancreatic obstruction of the bile ducts)

645
Q

What treatments are used for lead poisoning? What about arsenic, mercury or gold poisoning?

A

EDTA for lead, also can use dimercaprol and succimer for all of the above.

646
Q

What is the mechanism of the drug used to treat latent TB infection?

A

Rifampin decreases messenger RNA synthesis by inhibiting bacteral DNA-dependent RNA pol

647
Q

What pathologic finding would lead to this liver biopsy?

A

This is a cirrhotic liver with micronodular cirrhosis (pink nodules surrounded by cirrhotic tissue) which is associated with persistent activation of stellate cells.

648
Q

What is the embryonal origin of the ductus arteriosus?

A

The sixth aortic arch

649
Q

How would you differentiate asbestosis from silicosis?

A

Both are restrictive lung diseases, however silicosis often presents with eggshell calcifications in the lymph nodes of the upper lobes of the lungs, whereas asbestosis is typically associated with lower lung pathology as well as increased risk of mesothelioma and bronchogenic carcinoma. Asbestosis industry associations are with shipbuilding roofing and plumbing.

650
Q

Which drugs are associated with crystal-induced nephropathy?

A

Acyclovir, sulfonamide antibiotics, ethylene glycol, megadoses of vitamin C, methotrexate, protease inhibitors.

651
Q

What is the blood supply to the ovary?

A

The ovaries receive blood from the ovarian arteries which are direct branches of the abdominal aorta.

652
Q

Infants of diabetic mothers are at greater risk of being born with this condition which causes early cyanosis.

A

Transposition of the great vessels.

653
Q

Why are grain products supplemented with this one – carbon transfer coenzyme?

A

Folate is important for the development of the neural tube by a closure of the neural folds at four weeks of pregnancy.

654
Q

What is the difference between methanamine (Gomori) silver stain and regular silver stain?

A

Methenamine silver = Pneumocystis jiroveci

Silver stain = Legionella pneuemophilia

655
Q

What is the mechanism of action for the drug used as primary treatment for shingles?

A

Famciclovir is activated by viral thymidine kinase into acyclovir monophosphate which is a nucleoside analog resulting in chain termination by viral DNA polymerase.

656
Q

What type of hypersensitivity reaction characterizes myasthenia gravis? What is affected?

A

Type II or direct, antibody-mediated hypersensitivity targeted to the postsynaptic AChRs

657
Q

Describe the three stages of Lyme disease progression

A
  1. Flulike symptoms and classic target shaped rash
  2. neurologic involvement including facial palsy, cardiac involvement (atrioventricular conduction delay)
  3. asymmetric arthritis or subacute encephalopathy (rarely)
658
Q

A characteristic daily fever spike accompanied by polyarthritis and a macular salmon pink rash, leukocytosis, anemia, and elevated ESR is most likely what disorder? What are the diagnostic criteria? What is the first referral that you need to do?

A

Systemic JIA, fevers must be present for more than two weeks and arthritis for more than six weeks. Should refer to ophthalmology to evaluate for uveitis.

659
Q

Distinguish between fetal presentations of remnants in the posterior urethra versus ureteropelvic junction obstruction.

A

You PJ obstruction is typically unilateral hydronephrosis with dilatation proximal to the obstruction (i.e. not of the bladder). A persistent urogenital membrane will present as posterior urethral valves at the junction of the bladder and urethra.

660
Q

What is heparin induced thrombocytopenia? What is the appropriate treatment?

A

Typically occurring 5 to 14 days after heparin use, IgG antibodies against heparin bound platelet factor for leads to platelet activation, clot formation, and thrombocytopenia.

Treatment is stopping heparin and giving direct thrombin inhibitors such as are argatroban or lepirudin.

661
Q

What is the most specific autoantibody for rheumatoid arthritis?

A

Anti-CCP (citrullinated protein)

662
Q

Name this tumor found in an eight year old boy. What are the key characteristics?

A

Well-circumscribed tumor with a large cystic component and a brightly enhancing mural nodule. Typically found in the posterior fossa, this is a (benign) pilocytic astrocytoma, the most common primary brain tumor in children

663
Q

What drugs are known to cause drug-induced lupus erythematosus?

A

Hydralazine, procainamide, TNF alpha inhibitors (etanercept), methyldopa, isoniazid, phenytoin.

664
Q

A rapid deceleration injury is most concerning for what vascular trauma?

A

Rupture of the aortic Isthmus, just distal to the left subclavian.

665
Q

What is the vascular origin of the following hemorrhages?

  1. Epidural hematoma
  2. subdural hematoma
  3. subarachnoid hemorrhage
  4. intra-parenchymal hemorrhage
A
  1. Rupture of the middle meningeal artery
  2. rupture of the bridging veins
  3. ruptured berry aneurysm
  4. intraparenchymal hemorrhage which is atraumatic is typically caused by hypertension but can also be due to amyloid and uropathy or recurrent lobar hemorrhagic strokes, vasculitis, or neoplasm.
666
Q

A woman presents with progressive proximal muscle weakness without pain, fatigability, or rash. What is the most likely diagnosis? What are characteristic findings on investigations? What is the treatment?

A

Polymyositis associated with endomysial infiltration of CD8 positive T cells and overexpression of MHC class I.

On investigations elevated creatine kinase, antinuclear antibody, anti-jo-1, anti-SRP, anti-Mi-2. Muscle biopsy shows Perimysial infiltration. Vesicular atrophy with patching necrosis. Can occur in a paraneoplastic syndrome associated with ovarian adenocarcinoma, lung cancer, colorectal cancer, and non-Hodgkin lymphoma.

Corticosteroids are first-line treatment.

667
Q

What are the characteristic findings of the disease associated with this intestinal biopsy? What is the classic presentation and findings on investigation?

A

Associated with northern European descent, steatorrhea, iron deficiency anemia (refractory to treatment).

Also associated with dermatitis herpetiformis which is characterized by clusters of pruritic, papular or bullous lesions on the trunk and extensor surfaces.

Intestinal biopsy will show villus blunting with crypt hyperplasia and lymphocytic infiltration into the lamb you propria.

Investigations positive for antiendomysial or anti-TTG antibodies.

668
Q

What is the diagnosis based on this intestinal biopsy from a patient with a history of abdo pain and bloody diarrhea, as well as tender, erythematous bumps on the shins.

A

This shows a noncaseating granuloma consistent with Crohn’s disease.

669
Q

Distinguish between spermatocele, hydrocele, and varicocele

A
  1. Spermatocele: a cyst due to dilated epididymal duct or rete testis. It is a painless, paratesticular fluctuant nodule
  2. Hydrocele is a fluid collection in the scrotum which transilluminates
  3. Varicocele is the “bag of worms” dilated veins in the pampiniform plexus of the testicle, which normally cools the testes (can lead to fertility problems), painful, does not transilluminate.
670
Q

What drugs are associated with ATN?

A

Antibiotics: Aminoglycosides, beta-lactams, rifampin and vancomycin

Antivirals: Acyclovir, cidofovir, tenofovir, foscarnet

Other: cisplatin, contrast dies, IVIg

671
Q

What adverse effects are associated with piperacillin? What are the target organisms?

A

antipseudomonal. Associated with hypersensitivity reactions and interstitial nephritis (eosinophils on UA)

672
Q

What are complications of untreated Graves’ disease?

A

Chronic proptosis/lid retraction can lead to corneal ulceration and blindness

Thyroid-stimulating immunoglobulins also can cause pretibial myxedema (big red rash on legs)

Osteoporosis (due to stimulation of osteoclast activity)

Neonatal hyperthyroidism (in pregnant patients)

673
Q

What is the appropriate treatment for Lyme in pregnant patients or children < 8yo?

A

Amoxicillin

674
Q

A family history positive for leukemia, adrenal and breast cancer at a young age is most likely caused by a mutation in which gene?

A

TP53 (this is Li-Fraumeni syndrome).

675
Q

What is the defective enzyme and presentation of metachromatic leukodystrophy? What are the findings on biopsy?

A

Arylsulfatase A, causing accumulation of cerebroside sulfate, which causes metachromasia (toluidine blue appears reddish/pink). Biopsy will also show evidence of demyelination.

Classic presentation is regression or developmental delay in gross motor i.e. muscle weakness.

676
Q

What are the effects of a nonspecific beta-blocker (e.g. nadolol)

A

Beta1 + Beta2 antagonism; B1 is cardiac so decreased HR, contractility and renin release, B2 is vascular; inhibition causes vasoconstriction and increased systemic vascular resistance.

677
Q

What is the bacterial component that is used for Haemophilus influenzae vaccine?

A

The polyribosylribitol phosphate (type B polysaccharide) capsule.

678
Q

Where on the tRNA does is the amino acid attached?

A

The 3’-CCA amino acid acceptor site.

679
Q

What findings on ABG would you expect to see in a patient with a PE?

A

Respiratory alkalosis + hypoxemia

High: pH

Low: PCO2 and PO2

Unchanged: HCO3 (not enough time for compensation)

680
Q

How do you interpret UA findings with suspected UTI?

A

+ve leukocyte esterase = WBCs

+ve nitrite = gram-negative bacterial species e.g. E. coli (most common cause of UTI)

+ve urease test = Staph saprophyticus, Proteus, Klebsiella

681
Q

Pigmented cartilege and dark urine is caused by what enzyme deficiency?

A

Alkaptonuria due to deficiency of homogentisic acid oxidase (tyrosine degradation pathway).

682
Q

What hormone disruptions are present in the setting of PCOS?

A

High LH and insulin resistance, leading to hyperinsulinemia, hyperglycemia and hyperlipidemia.

683
Q

Where do aspirated foreign objects usually end up in the lung?

A

Right lung mainstem bronchus (and further into the intermediate bronchi if it’s small).

684
Q

What treatment can be used to prevent cluster headaches?

A

verapamil

685
Q

At what age is an upgoing Babinski normal?

A

<12 months of age.

686
Q

What are the signs/symptoms of Guillain-Barré Syndrome? What might you be worried about on ABG?

A

Ascending weakness/paralysis, steppage gait (foot drop), leading to respiratory paralysis.

Hypoventilation -> respiratory acidosis = LOW pH, High CO2 and no change in HCO3.

687
Q

What is the first-line treatment for delirium?

A

Treat the underlying condition, give a low-dose antipsychotic (e.g. haloperidol).

688
Q

Why is isoniazid not used as monotherapy in active TB?

A

Monotherapy increases the risk of developing resistant TB due to mutations lowering activity of bacterial catalase peroxidase.

689
Q

What is the mechanism of action of infliximab, etanercept or adalimumab?

A

Binds TNF-alpha and blocks activity. Does not target the TNF-receptor

690
Q

What is the etiology and diagnosis in this young boy who presents with multiple hamartomatous polyps in the small intestine?

A

Peutz-Jehgers syndrome, caused by mutations in STK1. Hyperpigmented macules can also present in/on lips, mouth, hands and genitalia

691
Q

What is the classic presentation of diverticulitis? What is the finding on histology? On imaging?

A

`Crampy LLQ abdo pain with diarrhea and a fever.

Focal areas of weakness in the muscularis propia

Pericolic fat staining + Thickened colonic wall.

692
Q

What is the differential for a megaloblastic anemia? How do you distinguish between etiologies?

A

Either vitamin B12 or folate deficiency. Diet-related more likely to be folate as stores more rapidly depleted. B12 deficiency also presents with neurologic symptoms including numbless, paresthesias or gait abnormalities (B12 is a cofactor for methylmalonyl CoA mutase)

693
Q

What si the effect of angiotensin II on the efferent renal arteriole cells?

A

Ang II -> Gq receptor -> increased PLC

694
Q

What is a zenker diverticulum?

A

A false diverticulum presenting in elderly men between the thyropharyngeal and cricopharyngeal parts of th e inferior pharyngeal constrictor.

695
Q

How does GERD present in an infant?

A

Persistent wheezing, night-time cough, decreased appetite, poor weight gain and intermitted regurgitation.

696
Q

What prophylaxis should be given to persons with large BSA burns?

A

Omeprazole or PPI to prevent a Curling ulcer (a fundal ulcer)

697
Q

What is growing on this culture? What is the virulence mechanism?

A

Pseudomonas aeruginosa; makes exotoxin A which ADP ribosylates + inhibits EF2, stopping protein synthesis.

698
Q

What therapy is indicated for post-streptococcal glomerulnephritis?

A

Supportive therapy only; some role for prednisone in very severe cases with renal failure.

699
Q

What is the diagnosis? What would you see on utrasound bfore birth?

A

Tracheoesophageal fistula; 2/3 of cases present with polyhydramnios.

700
Q

Which AIDS-defining illness is associated with an encapsulated yeast with narrow-based budding? What is the vector associated with transmission?

A

Cryptococcus neoformans meningoencephalitis.

Pigeon droppings (e.g. “city garden”)

701
Q

What fungal infection is characterized by a small intracellular yeast? Where is it typically found? What’s the transmission vector? What would you see on pathology?

A

Histoplasmosis, found in the Mississipi and Ohio river valleys and commonly tranmitted by bird and bat droppings. Lung granulomas with calcifications.

702
Q

What is this fungus? What are the key characteristics?

A

Aspergillus fumigatus

Mold with septate hyphae that branch in a V-shaped 45-degree angle

703
Q

Name this fungus. What are its special characteristics? Where is it found? What are the symptoms?

A

Blastomyces: it’s a dimorphic fungus (mold in the cold, yeaste in the heat). Found in soil in wooded areas east of the Mississippi River.

Symptoms of pneumonia: cough, fever, shortness of breath, sometimes hemoptysis.

704
Q

Name the organism: a budding yeast with pseudohyphae?

A

Candida albicans

705
Q

How is glucose sensed by the pancreatic beta islet cells?

A

Glucose enters beta cells by GLUT2. When glucose falls, ATP levels fall, leaving ATP-sensitive K+ channels open.

When glucose levels rise and K+ channels close, membrane depolarization leads to Ca2+ entry into the cell and activation of exocytosis of insulin granules

706
Q

Which cancers is a RET mutation associated with?

A

MEN-2A is Parathyroid hyperplasia or tumor -> hypercalcemia

MEN-2B marfinoid habitus, ganglioneuromas in mounth / GI tract.

Both: medullary carcinoma of the thyroid, pheochromocytoma.

707
Q

How do you differentiate between actue stress disorder and PTSD?

A

Acute stress disorder is a disturbance in function associated with a traumatic event between 3days and 1 month post-event. PTSD is >1 month.

708
Q

Describe the timelines and pathology of different types of graft rejection.

A

Hyperacute (minutes to hours) due to pre-existing antibodies reacting with donor antigen -> graft vessel ischemia and necrosis

Acute (weeks to months) due to activation of T cell activation against donor MHCs -> vasculitis with lymphocytic infiltrate

Chronic (months to years) -> CD4+ T cells respond to recipient APCs presenting donor peptides -> proliferation of vascular smooth muscle, parenchymal atrophy, interstitial fibrosis

Graft-versus-host: Grafted T cells proliferate and reject host cells -> symptoms include maculopapular rash, jaundice, diarrhea and hepatosplenomegaly.

709
Q

What is rotor syndrome?

A

AR disease with conjugated hyperbilirubinemia caused by impaired uptake and excretion of bil (without abnormal pigment in hepatocytes).

Similar to Dubin Johnson.

710
Q

How would you treat a patient on an antipsychotic who presents with fever, muscle rigidity and tachycardia?

A

This is neuroleptic malignant syndrome, and can be treated by muscle relaxants e.g. dantrolene (which blocks Ca2+ release from SR).

711
Q

How would you differentiate between toxoplasmosis or CMV infection in HIV patients?

A

CNS Toxoplasmosis typically presents with encephalitis, focal neurlogic deficits and a ring-enhancing lesion + mass effect.

CMV casues retinitis + diarrhea, but not a specific visual field cut and not typically seizures.

712
Q

What disease presents with mixed upper/lower motor neuron findings in the extremities? What pathology would you see in the spinal cord?

A

Amyotrophyc lateral sclerosis (ALS) with degeneration of the anterior horns of grey matter (LMN symptoms of weakness, atrophy and fasciculations) and corticospinal tracts (UMN symptoms i.e. hyperreflexia)

713
Q

Which antibiotics act at the 30S subunit of the bacterial ribosome? The 50S subunit?

A

buy AT 30, SCELL at 50

30S: aminoglycosides and tetracyclines

50S: Streptogramins, Chloramphenicol, Erythromycin (macrolides), Clindamycin and Linezolid

714
Q

What is the cause of these lesions in this HIV+ve individual? What other symptoms may occur? What is the treatment?

A

These lesions are characteristic of Kaposi sarcoma (HHV-8). Other symptoms include lymphedema or spread to oral mucosa, GI or respiratory tract.

Therapy is continued HAART, but can inject vinblastine or provide interferon-alpha or systemic chemo if severe.

715
Q

Where is the fluid localized in a testicular hydrocele?

A

Between the parietal and visceral layers of the tunica vaginalis.

716
Q

Describe the bacterial characteristics of the most common causes of meningitis in the neonate.

A

E. coli: gram -ve bacillus, lactose fermenting

L. monocytogenes gram+ve bacillus, catalase +ve

GBS: gram +ve cocci in chains, beta-hemolytic, catalase-negative, and facultative anaerobe

717
Q

Describe the key differences between and HMO or a PPO (preferred provider organization) plan.

A

HMO -> care coordinated through PCP and specialists require a referral, no coverage out-of-network, have lower premiums

PPO -> Can choose any provider and book appointments with specialists directly. Will reimburse out-of-network but higher premiums

718
Q

What type of stones is most common in people with Crohn disease? What urine pH are they associated with?

A

Calcium oxalate stones—acidic urine

719
Q

What embryological structure forms the scrotum? What does it form in girls?

A

The labioscrotal swelling (forms labia majora in girls)

720
Q

What drugs are associated with avascular necrosis of the femoral head?

A

Long-term systemic steroid use

721
Q

What symptoms are suspicious for carcinoid syndrome? What would you find on UA?

A

Wheezing, with episodes of facial flushing and diarrhea

5-hydroxyindoleacetic acid.

722
Q

What do each of the following nuclei of the hypothalamus regulate?

Lateral nucleus

Supraoptic nucleus

Ventromedial nucleus

Posterior nucleus

A

Lateral nucleus - hunger

Supraoptic nucleus - osmoreceptors (also in the paraventricular nucleus)

Ventromedial nucleus - eating

Posterior nucleus - thermoregulation

723
Q

When would you use ezetimibe? Gemfibrozil? Cholestyramine? What are their mechanisms

A

Ezetimibe (PCSK9 inhibitor) can be used when patients have high LDL that isn’t well controlled by statins

Gemfibrozil is a fibrate that decreases triglyceride levels (note increases risk of rhabdo when combined with a statin)

Cholestyrmamine (bile acid resin) binds bile acids and reduces uptake, but also reduces uptake of other meds.

724
Q

What part of the GI tract is most at risk during a AAA repair?

A

The sigmoid colon, due to the IMA branch point location along the aorta.

725
Q

What are the symptoms of phenylketonuria (PKU)?

A

Strange odor, pale skin, hyperreflexia, developmental delay and eczematous rash.

726
Q

What lesion produces a positive Romberg?

A

the medial lemniscus (disrupts contralatal proprioception)

727
Q

What symptoms are consistent with primary adrenal insufficiency? What test can be done as part of the workup?

A

Hypotension, weight loss, gum hyperpigmentation, hyponatremia and hyperK+.

Can use metyrapone to decrease serum cortisol (blocks conversion from 11-deoxycortisol). In primary insufficiency, the ACTH goes up as cholesterol goes down; in secondary insufficiency the ACTH doesn’t compensate for the drop in cortisol.

728
Q

What infection in an individual with AIDS could result in vision loss? How would you treat?

A

CMV retinitis; treat with Ganciclovir

729
Q

What are the toxicities of ganciclovir?

A

Leukopenia, neutropenia, thrombocytopenia and hemolytic anemia

+ nephrotoxicity

730
Q

How does dwarfism differ from GH deficiency?

A

In GH deficiency, limbs and heads will be proportionately smaller, dwarfism has disproportionately large heads and short limbs

731
Q

What gene is associated with dwarfism? What is the inheritance and risk factor for mutations?

A

FGFR3 gain of function, autosomal dominant, advanced paternal age.

732
Q

What is the histology characteristic of subacute thyroiditis?

A

Inflammatory infiltrate with multinucleated giant cells

733
Q

Tall, crowded follicular epithelial cells with scalloped colloids are diagnostic for what thyroid disease?

A

Graves disease

734
Q

What is the characteristic histology of toxic multinodular goiter?

A

Focal patches of hyperfunctioning follicular cells distended with colloid

735
Q

What is Reidel thyroiditis?

A

Thyroid tissue replaced with inflammatory infiltrate (fibrosis / fibrosclerosis) -> hypothyroidism.

736
Q

What are the six criteria for allergic (eosinophilic) granulomatosis with angiitis?

A

Asthma

Eosinophilia

Paranasal sinusitis

Pulmonary infiltrates

Vasculitis + extravascular eosinophils

Polyneuropathy

4/6 for diagnosis with pANCA

737
Q

What is the physiologic function of vasoactive intestinal peptide?

A

Increases water + electrolyte secretion into lumen and relaxes smooth muscle and sphincters.

738
Q

Hypersegmented neutrophils is characteristic of what deficiency?

A

Folic acid deficiency

739
Q

What is abnormal about this ECG? What is the cause?

A

Peaked T waves, characteristic of hyperkalemia

740
Q

When you are converting a probability to a percentage, what do you have to be careful of?

A

Make sure you multiply by 100 when converting to a percentage.

741
Q

What is viral complementation?

A

When one virus lacks a necessary protein to replicate and borrows it from a co-infecting virus or other source.

742
Q

How do you differentiate clinically between IgA nephropathy and post-strep glomerulonephritis?

A

Timing of symptoms: IgA nephropathy is concomittant with infection, whereas PSGN is 3-6 weeks after infection.

Additionally, complement decresases in PSGN but not in IgA nephropathy.

743
Q

Differentiate between the cause and presentation of post-streptococcal glomerulonephritis and rheumatic fever

A

PSGN presents with kidney changes, rheumatic fever does not.

RF is caused by GAS infection and cross-reactivity of antibodies; PSGN is due to type III reaction with immune complex deposition

744
Q

What causes palmar erythema and spider angiomas with liver disease?

A

Hyperestrinism

745
Q

Differentiate between Alport disease and Goodpasture syndrome

A

Alport is an inherited disease due to mutation of collagen IV leading to sensorineural hearing loss, ocular defects and hematuria, Goodpasture is due to autoimmunity against glomerular basement membrane + can have alveolar involvement leading to hemoptysis.

746
Q

Describe the arm movement of the subscapularis muscle

A

Adduction and internal rotation

747
Q

How does infraspinatus and teres minor move the arm?

A

Both externally rotate; teres minor adducts.

748
Q

Differentiate primary myelofibrosis and essential thrombocythemia

A

primary myelofibrosis initially presents with myeloid proliferation followed by fibrosis and loss of hematopoetic cells (dacrocytes).

Essential thrombocythemia is a diagnosis of exclusion with isolated high levels of megakaryocytes and platelets (some abnormal on blood smear)

749
Q

What symptoms would you expect from someone with this jejunal biopsy?

A

Migratory arthritis, abdo pain, steatorrhea, weight loss

Caused by whipple disease (Tropheryma whipplei)

750
Q

What is the mechanism of action of bactracin? What is it used for?

A

Inhibits translocation of D-ala-D-ala to the outside of the bacterial cell. Used topically due to high risk of nephrotoxicity if administered IV.

751
Q

What is the classic presentation of aspirin-induced asthma? How is it differentiated from allergies?

A

Aspirin intolerance, nasal polyps, and adult-onset asthma.

Allergies are typically presented with sneezing and itchy red eyes as well as seasonal association.

752
Q

What process limits airflow during forced expiration?

A

Positive pleural pressure compresses the airways, leading which limits airflow.

753
Q

What hormone causes the basal body temperature to increase after ovulation?

A

Progesterone

754
Q

What is the mechanism of action and side effect of glyburide?

A

Increases pancreatic insulin by depolarizing beta cells; causes hypoglycemia.

755
Q

What medications can be used to treat Graves disease? What is their mechanism of action?

A

Thioamides (propylthiouracil and methimazole) block iodination of tyrosine and inhibit thyroid peroxidase (coupling).

756
Q

Which arteries are spared in polyarteritis nodosa?

A

The pulmonary arteries

757
Q

What are the side effects of clozapine? What is its indication?

A

Drug-induced agranulocytosis, mouth and throat ulcers, myocarditis, weight gain, sialorrhea. Used for refractory schizophrenia (esp. as it has less tardive dyskinesia)

758
Q

Distinguish between neurofibromatosis type 1 and 2.

A

Type 1: due to neurofibromin mutation (chr. 17) leading to cafe-au-lait spots (>6), axillary and inguinal freckles, iris hamartomas (Lisch nodules), neurofibromas and optic gliomas.

Type 2: due to merlin mutation (chr 22) leading to bilateral vestibular schwannomas / oth CN schwannoma, intracranial meningioma, peripheral neuropathy, cataracts and cutaneous tumors.

759
Q

What metabolic disturbance can be caused by metformin?

A

Lactic acidosis (AGMA) due to increased lactic acid production in intestines and reduced hepatic gluconeogenesis (must check kidney function)

760
Q

Which hematoma crosses suture lines? which does not? What other symptoms may accompany the latter?

A

Subdural hematoma = cross suture lines

Epidural hematoma does not; presents with lucid interval, increased ICP can cause uncal herniation leading to ipselateral CN III palsy.

761
Q

Histologically, what would you see in someone with fistula, crampy abdominal pain and a positive guiaic test.

A

Noncaseating granulomas and transmural inflammation (crohn disease)

762
Q

A positive rapid plasma reagin test (or VDRL test) with a negative treponemal antibody test should make you think about?

A

SLE (they should both be positive in syphilis

763
Q

What is the difference between actinic keratosis and seborrheic keratosis?

A

SK is flat, greasy and pigmented and typically a benign neoplasm in older adults

AK is a precancerous lesion consisting of a small, rough, erythematous/brown papule//plaque.

764
Q

What drug must be administered alongside imipenem? What is its mechanism of action?

A

Cilastin, which inhibits dehydropeptidase-1, a PCT enzyme which metabolizes imipenem.

765
Q

What is psittacosis? What would you see on histology?

A

Pneumonia with fever, headache, malaise and non-productive cough. Due to Chlamydophilia psittaci infection, typically carried by birds.

Giemsa stain shows cytoplasmic inclusion bodies.

766
Q

What causes mumps? What is the typical presentation?

A

RNA paramyxovirus infection causis parotitis, orchitis, pancreatitis (can present with acute epigastric pain) and meningitis.

767
Q

What protozoal infections are treated with metronidazole? Which are treated with praziquantel?

A

Metronidazole for GET GAP (Giardia, Entamoeba, Trichomonas, Gardnerella vaginalis, Anaerobes and H pylori (if allergic to penicillin).

Praziquantel for schistocytosis and cestodes (tapeworms)

768
Q

Hemorrhagic cystitis in someone treated with cyclophosphamide is associated with what condition?

A

Fanconi anemia (sensitivity due to chromosomal breakage in response to DNA-damaging agent).

769
Q

How are helper T cells activated? What occurs with incomplete activation?

A

2 signals req’d for activation: presentation of antigen via MHC class II APC and a co-stimulatory signal via B7 protein (CD80/86) which interacts with CD28 on T cell.

Without the latter signal, T cell becomes anergic and refractory to future stimulation (peripheral tolerance).

770
Q

Describe the sequence of events that leads to anaphylactic shock

A

Cross-linking of IgE receptors on mast cells and basophils leads to degranulation -> vasodilation and leaky capilaries.

771
Q

People who are obtunded or with history of alcoholism are at increased risk for what kind of infecitons? What pathogens are responsible?

A

Aspiration pneumonia caused by Peptostreptococcus, Bacteroides fragilis, Prevotella

772
Q

Describe the 5 components of the Apgar score

A

Activity (extremity movement)

Pulse

Grimace (irritability in response to nasal suction)

Appearance (cyanosis)

Respiration

773
Q

How would you distinguish between the two major causes of bleeding post 20-weeks gestation?

A

Placenta previa = painless bleeding

Abruptio placentae = painful bleeding, typically accomanied by uterine contractions and fetal distress.

774
Q

What is the diagnosis for flu-like sympoms + enlarged cervical lymph nodes and splenomegaly? What is the causative virus?

A

Infectious mononucleosis caused by EBV

775
Q

Differentiate between ITP and TTP

A

Idiopathic thrombocytopenic purpura, due to antibodies against platelet antigens causes isolated thrombocytopenia and petechia.

Thrombotic thrombocytopenic purpura due to antibodies against ADAMTS13 protease (vWF metalloproteinase). FAT RN Fever, maha, thrombocytopenia, renal failure and neurologic disturbance.

776
Q

What paraneoplastic syndrome is associated with squamous-cell carcinoma? What is the classic presentation?

A

Hilar mass with cavitation, productive cough and weight loss; smoking.

Excess parathyroid hormone related peptide leading to hypercalcemia (stones, thrones, groans and psychiatric overtones).

777
Q

When considering sympotms in an individual with substnace use disorder, what is it important not to forget?

A

Make sure that you rule out an organic cause for symptoms rather than focussing on a substance-use etiology

778
Q

What drugs used to treat MI are contraindicated with recent cocaine use?

A

Beta-blockers (esp. nonselective), because of the incerase in norepinephrine due to cocaine leading to unopposed alpha effects = vasoconstriction

779
Q

What are the indications for treatment of a suspected viral meningitis?

A

Supportive care & observation unless

  1. Elderly / immunocompromised (treat for bacterial until CSF cultures back)
  2. Signs of HSV infection (e.g. genital lesions or PCR tests)
780
Q

Which drugs cause pulmonary fibrosis? How would you differentiate their presentations?

A

Bleomycin (typically weeks-months)

Busulan (at least 4 years post-treatment) and also associated with significant myelosuppression

781
Q

What are ketoconazole and griseofulvin’s effects on CYP450

A

Ketoconazole inhibits CYP450

Griseofulvin induces CYP450

782
Q

What CNS tumor is associated with this histology?

A

Meningioma (benign tumor from arachnoid cells). Note the psammona bodies.

783
Q

How would you differentiate between aortic stenosis due to congenital cause versus sclerosis / aquired cause?

A

Congenital bicuspid valve presents with calcifications typically by age 50.

784
Q

What are the origins of the vertebral arteries?

A

Subclavian arteries.

785
Q

Damage to which nerve leads to vocal cord paralysis? What is the embryological origin of this nerve?

A

The recurrent laryngeal nerve arising from the 6th pharyngeal arch.

786
Q

What is the diagnosis in an AIDS patient with a single ring-enhancing lesion with CD20+ cells?

A

Primary CNS lymphoma due to EBV infection.

787
Q

What are the causes of hyperprolactinemia?

A

prolactinoma, antipsychotic drugs such as dopamine antagonists

788
Q

This patient presents with thrombocytopenia. What is the etiology?

A

Thrombotic thrombocytopenic purpura, due to antibodies against ADAMTS13 metalloproteinase

789
Q

What is the expected findings on investigation for primary sclerosing cholangitis?

A

Positive p-ANCA, elevations and alkaline phosphatase

790
Q

What investigations are expected to be abnormal in PCOS?

A

Glucose, high T, high LH:FSH ratio.

791
Q

Differentiate between adenocarcinoma of the esophagus and laryngeal squamous cell carcinoma

A

Typical presentation is dysphagia and weight loss\

Adenocarcinoma of the esophagus commonly associated with chronic GERD & progression from Barrett’s eso, smoking and obesity.

Laryngeal squamous cell carcinoma is associated with excessive tobacco + alcohol, horseness etc.

792
Q

What are the 1st generation sulfonylureas? What side-effects do they have? What are they used for?

A

chlorpropamide & tolbutamide

Disulfiram like reaction, weight gain

Used to incr insulin secretion.

793
Q

What is Leber hereditary optic neuropathy? What is the pattern of inheritance?

A

Progressive blindness in young adult men; may have movement disorders, arrhythmias, MS-like syndrome.

Mitochondrial inheritance

794
Q

What is the differential for this blood smear?

A

Megaloblastic anemia (note hypersegmented neutrophyl) due to folate deficiency or B12 deficiency.

795
Q

What is the diagnosis? What immunodeficiency worsens the disease?

A

Leprosy (M. leprae), with interferon-gamma deficiency.

796
Q

What is the pathogen which is most likely to cause this infection? What is it called?

A

HPV 6 / 11

condyloma acuminata

797
Q

What infections can chlamydia cause in the newborn?

A

pneumonia and bacterial conjunctivitis

798
Q

How does a congenital toxoplasmosis in the neonate present?

A

chorioretinitis.

799
Q

What type of hypersensitivity reaction is a transfusion reaction?

A

Type II (IgG antibodies cause complement lysis of RBCs)

800
Q

In addition to the classic triad of conjunctivitis, urethritis and arthritis, what other symptom can accompany reactive arthritis?

A

Sacroiliitis

801
Q

What investigations can be done to diagnose paroxysmal nocturnal hemoglobinuria? What defect causes the disease?

A

elevated urine hemosiderin;

Defect in the PIG-A glycosyl phosphatidylinositol (GPI) anchor leading to binding of CD55 / CD59 complement-inhibiting proteins -> complement-mediated hemolysis.

802
Q

What is the diagnosis based on this blood smear? What symptoms and labs would you expect?

A

AML (note auer rods).

Symptoms hematuria, diffuse petichiae, chest pain and SOB

Labs low platelets, high D-dimer, low fibrinogen (DIC)

803
Q

What is the cause and symptoms of renal osteodystrophy?

A

CKD + dialysis leading to joint pain, bone pain and multiple fractures.

Due to reduced GFR leading to reduced phosphate excretion -> hypocalcemia -> PTH

As well low D3 due to reduced a1-hydroxylation of D2

804
Q

What test is diagnostic of B12 deficiency, even in the absence of an elevation in MCV?

A

Methylmalonic acid elevation

805
Q

What are the autoantibodies produced in Graves disease?

A

thyrotropin receptor stimulatory antibodies

806
Q

What immunodeficiency is associated with mycobacterial infections?

A

IL-12 receptor deficiency (or defect in interferon signalling)

807
Q

What lesion is classically assocaited with prosopagnosia?

A

Right inferior temporal lobe lesion

808
Q

Where is the lesion in an upper homonymous quandrantanopia?

A

Lower devision of the geniculocalcarine tract (meyer loop) (contralateral)

809
Q

What is the lesion in a right inferior quandrantanopia?

A

Superior division of the calcarine sulcus, contralateral

810
Q

What is the etiology of autoimmune hemolytic anemia?

A

Complement binds to the Ch2 region (Fc) of IgG

811
Q

What are the common side-effects of protease inhibitors (for HIV treatment)?

A

Fat redistribution, hyperlipidemia, hyperglycemia, nausea, diarrhea, nephropathy and hematuria.

812
Q

What is this finding? What condition is it found in?

A

Lisch nodules, found in neurofibromatosis type 1

813
Q

What does the NF-1 gene produce?

A

neurofibromin, a GTPase-activating protein that decreases Ras signalling

814
Q

What are the characteristics of hunter syndrome? How do you differentiate it from hurler syndrome?

A

Pearly, papular skin eruptions, a deep hoarse voice, skeletal abnormalities, distended abdo and diarrhea.

Cornea clouding found only in hurler syndrome

815
Q

What are the characteristics of Niemann-Pick syndrome?

A

Hepatosplenomegaly, foam cells, cherry-red macular spots

816
Q

What differentiates congenitally acquired rubella from CMV?

A

Rubella: blueberry muffin rash, cataracts, hearning loss, PDA

CMVO IUGR, CNS damage with hearing/vision impairment, periventricular calcifications on CT, microcephaly and intellectual disability.

817
Q

What is the pulmonary capillary wedge pressure?

A

Measures left atrial / left ventricular end-diastolic pressure. Not affected by lung pathology?

818
Q

What is the differential for S3 vs S4?

A

S4 is diastolic HF including concentric LVH and AA amyloidosis (restrictive cardiomyopathy)

an S3 is found in dilated cardiomyopathy with systolic failure and reduced ejection fraction.

819
Q

Which vaccines induce only humoral immunity?

A

RIP always

Rabies, Intramuscular Influenza, Polio (salk, not oral) and hep A

Due to use of killed/inactivated virus

820
Q

What are the characteristics of the bacterium which causes rocky mountain spotted fever?

A

Rickettsia rickettsii is a gram-negative obligate intracellular cocobacillus, which is transmitted by tick bites.

821
Q

What CNS tracts are affected by B12 deficiency?

A

Degeration of myelinated neurons in the dorsal columns, later corticospinal tracts and spinocerebellar tracts.

822
Q

What is 2nd line therapy for patients with Alzheimer dementia who fail acetylcholinesterase inhibitors? What is the mech of action?

A

Memantine, an NMDA antagonist (prevents excitatory neurotox).

823
Q

How do you calculate a 95% confindence interval for the mean in a normal distribution from SD?

A

CI = mean +/- Zx SEM

SEM = SD / sqrt(n)

824
Q

What are the risk factors for peptic ulcer disease?

A

H pylori, NSAID use, smoking.

NOT nitrites

825
Q

How do you differentiate between Parkonsons and normal pressure hydrocephalus?

A

PD has a narrow-based shuffling gait and NPH has a wide based magnetic gait.

other NPH symptoms include urinary incontinence and bradykinesia.

826
Q

A direct hyperbilirubinemia in the absence of findings other that jaundice or scléral icterus is suggestive of what disease? What is the appearance of the liver?

A

Dubin-Johnson syndrome, black liver

827
Q

How would you differentiate between chlamydia and gonorrhoea urethritis

A

Gonorrhoea has purulent discharge and is gram negative diplococci characterized by antegenically variable pili. Chlamydia does not gram stain and is an intercellular bacterium

828
Q

What are the key symptoms of diffuse large B-cell lymphoma?

A

fatigue & weight loss with a splenic mass.

829
Q

What is the mechanism of action of senna glycoside?

A

Increases peristalsis (stimulant laxative).

830
Q

Describe the difference between direct and indirect Coombs tests.

A

Direct = mixing of fetal blood with anti-IgG antibodies to decect presence of maternal antibodies attached to fetal cells.

Indirect = mixing of known Rh+ve RBCs with maternal serum, followed by anti-IgG serum (detects presence of maternal anti RhD antibodies

831
Q

What does the clock drawing test assess?

A

integration of multiple domains: orientation, comprehension, concentration, language, memory and visual-spatial awareness.

832
Q

What immunotherapy can be used for renal cell carcinoma and metastatic melanoma?

A

Recombinant interleukin 2 (adesleukin) which stimulates NK cells.

833
Q

What are the symptoms and treatment for serotonin syndrome?

A

3As:

Activity (clonus, hyperreflexia, hypertonia, tremor seizure)

Autonomic instability (hypertonia, diaphoresis and diarrhea)

Altered mental status

Treat with cyclohetadine.

834
Q

How would you differentiate between a problem with sertoli cells or leydig cells in finding an etiology for infertility?

A

Sertoli cells produce androgen binding protein, so low ABP makes them the culprit along with low T in semen.

835
Q

What substances stimulate the growth of hemangiomas?

A

Vascular endothelial growth factor (VEGF)

and Fibroblast Growth Factor (FGF)

836
Q

What is the mechanism of antibiotic resistance of MRSA?

A

Production of a modified penicillin binding protein.

837
Q

Identify the cells from this micrograph of cerebellum. What neurotransmitter do they secrete?

A

Purkinje cells

Inhibitory – secrete GABA

838
Q

What are risk factors for AAA?

A

Smoking, atherosclerosis, older age, male, FH.

839
Q

Levels of what substance would be increased in serum in megaloblastic anemia? Why?

A

Homocysteine (due to impaired conversion of homocysteine to methionine).

840
Q

exposures to which pathogens warrant use of passive immunization for postexposure prophylaxis?

A

Tetanus, botulism, hep B, varicella, rabies

“To Be Healed Very Rapidly”

841
Q

What is the difference between oppositional defiant disorder and conduct disorder?

A

ODD manifests as disobediance towards authority in the absence of serious violations of societal norms, e.g. aggression towards people and animals, destruction of property, deceitfulness/theft, serious rule violations.

842
Q

What symptoms are typically associated with hemolytic-uremic syndrome? What bacteria are most commonly associated? What is the virulence factor?

A

Symptoms: thrombocytopenia, microangiopathic hemolytic anemia, AKI

Bacteria: shigella and E.coli O157:H7

Virulence: Shiga-toxin which inactivates ribosomes, leading to cell death (B binds cells and lets A (toxic) in.)

843
Q

What is the Charcot triad of cholangitis? What might you see on labs?

A

RUQ pain, jaundice, fever.

inv: leukocytosis + neutrophilia

844
Q

What carcinoma would present with a neck mass which moves with swallowing and hypocalcemia?

A

Medullary carcinoma of the thyroid

845
Q

What is the infectious organism that is responsible for this rash? What is the risk factor for transmission?

A

N. meningitidis causing meningococcemia.

Often transmitted in close quarters.

846
Q

How do you distinguish between delayed sleep-wake phase disorder and insomnia?

A

Pts with insomnia typically have trouble falling asleep regardless of designated sleep time and often awaken in the middle of the night. With DSWPD, they can fall asleep at their desired sleep time; it’s more that there is a misalignment.

847
Q

What is the acronym for the derivatives of the pharyngeal arches?

A

When at the restaurant of the golden arches, children tend to chew, then smile, then swallow stylishly, or simply swallow, and then speak.

  1. Chew - maxillary, mandibular processes, malleus/incus, muscles of mastication
  2. Smile - stapes / styloid, lessor horn of hyoid, muscles of facial expression’
  3. Swallow stylishly - greater horn of hyoid and stylopharyngeus
  4. Aretynoids, cricoid, corniculate, cuneiform, thyroid, pharyngeal constrictors, cricothyorid, levator veli palatini
  5. speak - Intrisic muscles of larynx except cricothyroid
848
Q

Which chemotherapeutic agents are cell-cycle nonspecific?

A

Cisplatin / Pt agents

Alkylating agents: busulfran, cyclophosphamide, ifosfamide, nitrosoureas

849
Q

Differentiat between the symptoms typical of lesions of the cerebrocerebellum, vestibulocerebellum, or spinocerebellum.

A

Cerebrocerebellum: ipsilateral symptoms including dysdiadochokinesia and intention tremor.

Vestibulocerebellum, saccades / eye movements, posture, balance

Spinocerebellum, truncal ataxia

850
Q

What is the difference between rivastigmine and pyridostigmine?

A

Both are acetylcholinesterase inhibitors, however

Rivastigmine is used for dementia and is active in the CNS

Pyridostigmine is active in the PNS and can be used for myasthenia gravis treatment

851
Q

How would you differentiate between Hirschprung disease and imperforate anus in a newborn?

A

Rectal exam; Hirschprung gives a “squirt sign” which is forceful expulsion of stool on rectal exam, whereas you’ll see rectal distension in anal atresia.

852
Q

What are the symptoms of strongyloidiasis?

A

Eosinophilia (typical of parasitic infections), larva currens (mobile erythematus urticarial plaques), with cough and diarrhea.

853
Q

A thin blue line under the gums suggests what condition?

A

Lead poisoning

854
Q

Mixed LMN and UMN signs without sensory defecits is concerning for what condition? What is the location of the lesions?

A

ALS - amyotrophic lateral sclerosis

Typically presents with LMN first due to degeneration of anterior horn cells, followed by UMN due to degeneration of corticospinal tracts.

855
Q

What does this bowel CT scan show? What other symptoms would you expect?

A

Bowel thickening with pericolic fat staining, suggestive of diverticulitis due to microperforation of a diverticulum.

Other symptoms include a tender mass int he LLQ, worsening cramping pain, fever, nausea, constipation.

856
Q

What aditional layer of skin is present on the palms of hands and the soles of the feet and the dorsal distal phalanges?

A

Glabrous skin has a stratum lucidum.

857
Q

How does norepinephrine affect conduction velocity in the AV node and His-Purkinje system?

A

beta-1 adrenergic receptors -> increased Ca2+ influx into cells, reducing potential required for depolarization.

858
Q

What signs and symptoms are characteristic of psoas abcess? What is the most common organism involved? What are risk factors?

A

diffuse righ hip pain that gets better in a supine position with a flexed knee.

Most commonly caused by staph aureus

Risk factors include immunosuppression, secondary infection, recent surgery.

859
Q

What serum abnormality can be caused by long-term PPI usage?

A

hypomagnesemia

860
Q

What is the differential for these inclusions?

A

These are lewy bodies, found in Lewy body dementia and Parkinson disease.

861
Q

What prophylaxis can be offered to patients at risk of developing colon cancer?

A

Daily aspriin (which inhibits COX-2).

862
Q

how does the HSV1 virus reactivate?

A

Via travel from the cell body to axons via kinesin-dependent anterograde transport

863
Q

What is the preferred antidote for beta-blocker overdose? How does it work?

A

Glucagon, increases intracellular cAMP and increases Ca2+ release with muscle contraction.

864
Q

What side effect is associated with zidovudine?

A

anemia

865
Q

What is the inheritance pattern of neurofibromatosis type II?

A

Autosomal dominant

866
Q

What virus causes this common childhood lesion? What family does it belong to?

A

This is molluscum contagiosum, a poxvirus

867
Q

What bacteria can be visualized by Ziehl-Neelsen stain?

A

TB - mycobacterium tuberculosis

868
Q

What is the causative organism on this slide? What symptoms are expected?

A

Histoplasmosis caused by histoplasma capsulatum; common presentation is productive cough with green sputum, fever, headache, general malaise in someone who has exposure to contaminated soil with bird/bat droppings (ohio/mississippi valleys)

869
Q

What is Lidde syndrome? How do you treat it? What is the inheritance?

A

Due to GoF mutation leading to decreased ENaC degredation, increased Na+ resorption + hypoaldosteronism. Treat with triamterene or amiloride.

Inheritance is autosomal dominant

870
Q

An EFTS with low AFP, beta-HCG, Estriol, and normal Inhibin A indicates which genetic disorder?

A

Trisomy 18; Edwards

871
Q

What is the AFP pattern most concerning for Down Syndrome?

A

Low AFP, high betaHCG, low estriol, high inhibin A

872
Q

Which enzyme is most active with respect to glucose metabolism in the fasted state

A

fructose bisphosphatase 2

873
Q

An isolated low beta-HCG with normal other EFTS raises suspiscion for…

A

Trisomy 13, patau syndrome

874
Q

Which TCA metabolite is responsible for inhibiting phosphofructokinase and activating acetyl-CoA carboxylase? What is the net effect?

A

Citrate; decreased glycolysis and increased lipid synthesis

875
Q

What is the classification of a virus which causes koilocytes in tissue and genital warts?

A

Double-stranded, non-enveloped circular DNA virus; HPV.

876
Q

What is the inheritance pattern of von Willebrand disease? What shows up on labs? How do you treat it?

A

Autosomal dominant. On labs, increased bleeding and PTT time. Traet with desmopressin

877
Q

What are the monoamine oxidase inhibitors?

A

Tranylcypromine, phenelzine, isocarboxazid, selegiline (selective MAO-B)

MAO Takes Pride In Shanghai

878
Q

What is this finding from kidney biopsy stained with PAS? What other symptoms would you expect?

A

Crescentic glomerulonephritis, seen in Goodpasture syndrome. Cross-reactivity with resp. membranes leads to hemoptysis, anemia, and hematuria

879
Q

What is the organism on this silver-stained mucous membrane biopsy? What is the treatment?

A

Mucor (wide-branching nonseptate hyphae), treat with amphotericin B

880
Q

What is flucytosine used for?

A

Cryptococcal meningitis (in combination with amphotericin B) and candida infenctions.

881
Q

What is the typical presentation of phencyclidine use?

How is this differentiated from amphetamine use?

A

Agression, HTN, tachy, fever, horizontal nystagmus and hyperacusis

Amphetamines would present with pupilary dilatation.

882
Q

How do ACE inhibitors protect the kidney?

A

Reduction of ATII resulting in vasodilation preferentially of the efferent arteriole, reducing glomerular pressure.

883
Q

What treatment regimen is indicated for large B-cell lyphoma of limited stage?

A

R-CHOP

Rituximab + cyclophosphamide, doxorubiin, vincristine (oncovin), and prednisone

884
Q

Which prostate zone are most cancers found in?

A

The peripheral zone, adjacent to the rectum

885
Q

Describe the lesion. What is it most commonly associated with?

A

Punched-out soltary lesions with underlying tissues replaced by chronic inflammatory cells; characteristic of H. Pylori.

886
Q

What is winters formula for compensation for metabolic acidosis?

A

Predicted PCO2 = 1.5 x HCO3 + 8

887
Q

What treatment could you give for salicylate overdose?

How does it work?

A

Bicarbonate

Alkalinizes urine, thus promoting deprotonation of acidic drugs and favouring excretion

888
Q

Describe how the JVP corresponds to the cardiac cycle (see image)

A

a - atrial contraction

c - RV contraction

x - displacement of tricuspid down during ventricular ejection

v - filling of RA against closed tricuspid valve

y - RA emptying into RV

889
Q

What is a gluteus maximus gait? Damage to which nerve would most likely produce it?

A

Hips level, leaning back slightly with heel strike.

Inferior gluteal nerve

890
Q

How would you differentiate between tabes dorsalis and vitamin B12 deficiency?

A

B12 deficiency produces combination motor and sensory findings.

Tabes is also accompanied by other symptoms of neurosyphilis including overflow incontinence, lower extremity pain, Argyl Robertson pupill, sensory ataxia.

891
Q

How would you differentiate between H ducreyi and C trachomatis L1-L3 serotype infection?

A

chlamydia trachomatis type L1-L3 presents initially with a painless ulcer then regional lymphadenitis which is painful.

Ducreyi is going to present with a painful papule -> pustule -> ulcer ++lymphadenitis.

NO urethral discharge for either

892
Q

What is the diagnosis?

A

Paget disease of breast

893
Q

What risk factor and symptoms should raise suspiscion for prion disease?

A

Rapid progression of dementia + startle response and myoclonus.

Risk factors include cadaveric pituitary hormone, ingestion of infected brain tissue, dural, corneal and liver transplants.

894
Q

What is the effect of Milrinone? What is the mechanism of action?

A

Increased cardiac contractility and decreased peripheral vascular resitance

PDE-3 inhibitor

895
Q

In PKU, what neurotransmitter is affected?

A

Dopamine

896
Q

Name the class of drugs associated with letters B, C, and D

A

B - cholestyramine

C - HMG-CoA inhibitors

D - Fibrates e.g. gemfibrozil

897
Q

Describe the sensory distribustion of C2

A

posterior half of skull

898
Q

Describe the sensory distribution of C3

A

Turtleneck shirt.

899
Q

Describe the C4 dermatome

A

a low-collar shirt

900
Q

What is the pharyngeal arch which is associated with the intrinsic laryngeal muscles (except cricothyroid), artenoids and corniculate cartilage?

A

The 6th pharyngeal arch

901
Q

What is the age distribution for Hodgkin lymphoma? Non-hodgkin lymphoma?

A

Hodgkin lymphoma is typically 20-40yo

Non-Hodgkin is typically 65+

902
Q

Describe the arterial supply of the esophagus

A

Proximal 1/3 - inferior thyroid a

middle 1/3 bronchial artery + thoracic aorta

bottom 1/3 left gastric artery

903
Q

Identify the pathogen. How is it transmitted?

A

Leishmania donovi transmitted by the sandfly

904
Q

What are the symptoms and treatment of visceral leishmaniasis?

A

Symptoms: “black disease”, hepatosplenomegaly, malaise, pancytopenia, weight loss

treatment: sodium stibogluconate

905
Q

What is the first line treatment for Staph aureus?

A

1st gen cephalosporin e.g. cefazolin or dicloxacilin, oxacilin or nafcilin

906
Q

What is the mechanism of action and major side effect of chlormaphenicol?

A

Binding to 50S subunit; can cause grey baby syndrome and reversible bone marrow suppression

907
Q

Which polio vaccine is live attenuated? Which is killed?

A

Live attenuated is Sabin (oral)

Killed is Salk IM

908
Q

What are the key changes relative to point C that would produce A, B, D, or E?

A

A - Increased venous return (lower resistance) AND increased inotropy

B - Increased inotropy w/o change in venous return (e.g. digoxin, catecholamines (beta-1 agonist))

D - Negative inotropy due to narcotic overdose, beta-blockers, CCBs, dilated cardiomyopathy

E - increased total peripheral resistance (phenylephrine

909
Q

How would you differentiate between hunter/hurler syndrome and I-cell disease? What are the substances that accumulate in the former

A

Hunter (iduronate sulfatase) and hurler (a-L-iduronase) = glycosaminoglycans; urine mucoplysaccharides

I-cell disease = inclusion bodies and membrane-bound vacuoles, elevated serum lysosomal enzymes, affects fibroblasts

910
Q

What is appropriate renal testing for diabetic neuropathy?

A

urinary albumin excretion, as creatinine is only decreased in mid-late diseae

911
Q

What is the classic presentation of polyarteritis nodosa? What is the histologic appearance?

A

Fever, weight loss, myalgias, arthralgias, abdo pain, hypertension; elevations in ESR/CRP, leukocytosis

Fibrinoid necrosis of medium-sized muscular arteries.

912
Q

What syndrome would include tachycardia, hyperthermia, mydriasis, hyperreflexia and clonus? What drugs would cause it?

A

Serotonin syndrome

SSRI/SNRI, TCAs, MAO inhibitors

Triptans, tramadol, odansetron, linezolid, MDMA, dextromethorphan, meperidine, St. John’s Wort

913
Q

What is the key serum electrolyte disturbances in acute pancreatitis? What signs clinically would be suggestive of it?

A

Hypocalcemia; Chvostek or Trousseau sign

914
Q

How would you differentiate borrelia recurrentis infection from Brucella?

A

Borellia recurrentis has a relapsing fever that lasts 3-5 days with 7-9 day breaks in between and presents with jaundice, ecchymoses, change in LOC, neurologic findings, resp distress

Brucella - think unpastreurized dairy, undulant fever which is higher during the day and better at night, night sweats, weight loss, myalgias and arthralgias

915
Q

What is the characteristic urinary side effect of lithium toxicity?

A

Nephrogenic DI; low urine specific gravity (<1.01) and low osmolarity (<200mOsm/Kg) which is not corrected by ADH/vasopressin.

916
Q

What are the serum disturbances that would be expected in tumor lysis syndrome. How can you address/prevent them?

A

High potassium, phosphate and purines -> uric acid

Give rasburicase or allopurinol (NOT probenecid, you don’t want renal excretion from gout)

Hyperphosphatemia -> hypocalcemia, so may require additl Ca++

917
Q

What is the etiology of william syndrome?

A

Microdeletion of long-arm of chromosome 7

918
Q

What is the most likely etiology for someone presenting with back pain and this CXR?

A

Note cavitary lesion at lung apex -> TB

so Pott disease of spine

919
Q

If you have an erythema surrounding a catheter site and systemic infection, what is the most likely bug?

A

Staphylococcus epidermidis (coag neg staph)

920
Q

What are the urease-positive organisms?

A

Proteus, Cryptococcus, H pylori, Ureaplasma, Nocardia, Klebsiella, Staph epidermidis and saprophyticus

Pee CHUNKS

921
Q

Which enzyme is impaired in prolonged or high-dose nitroprusside treatment?

A

mitochondrial cytochrome C oxidase due to cyanide toxicity

922
Q

Which other cancers are pheochromocytomas associated with?

A

MEN2A - medulalary carcinoma of thyroid and parathyroid hyperplasia

MEN2B - medullary thyroid carcionma, mucosal neuromas, marfinoid habitus

923
Q

What is the difference in the mechanism of action of aminoglycosides and tetracyclines?

A

Aminoglycosides = irreversible binding to 30S subunit

Tetracyclines = reversible binding of 30S subunit (i.e. bacteriostatic vs bactericidal)

924
Q

How would you differentiate between hereditary spherocytosis and AIHA?

A

Hereditary spherocytosis tends to present with increased MCHC, AIHA may present with other cytopenias, or AIHA-adjacent conditions like SLE

925
Q

What interferon is useful for treating relapsing MS?

A

Beta-interferon

926
Q

What is interleukin-11 used for?

A

Treatment of thrombocytopenia

927
Q

What is the effect of norepinephrine on the heart?

A

Vasoconstriction -> increased diastolic filling -> increased CO, reflex bradycardia

928
Q

What is the characteristic x-ray of a giant cell tumor?

A

expansile osteolytic and radiolucent with sharp borders found in the distal epiphysis.

929
Q

What is the most common outcome of acute hep B infection? What are risk factors for chronic disease?

A

Immune clearance

Risk factors: <5 yo, immunosuppression.

930
Q

What is the most common complication of CMV retinitis?

A

Retinal detachment

931
Q

What diseases are due to frameshift mutations?

A

Duchenne muscular dystrophy and Tay-Sachs

932
Q
A
933
Q

Milky white blood is due to what deficiency? What is the causative substance?

What does it commonly present with?

A

Lipoprotein lipase defiency causing familial hyperchylomicronemia.

Acute pancreatitis

934
Q

When do the primitive reflexes disappear?

A

moro - 3 mos

root - 4 mos

palmar grasp - 6 mos

babinski - 24 mos

935
Q

What is a latent error?

A

Due to conditions of a healthcare setting that are “accidents waiting to happen”

936
Q

How would you differentiate between CAH due to 11-beta-hydroxylase vs 21-hydroxylase deficiency?

A

11-beta-hydroxylase deficiency results in 11-deoxcortisone overproduction -> HTN (due to mineralocorticoid effects)

21-hydroxylase deficiency presents with hypotension due to lack of mineralocorticoid production

937
Q

What are the cells that are activated 3-5 days post ischemic damage of CNS? 1-2 weeks?

A

3-5 days = activated microglia

1-2 weeks = activated astrocytes form glial scar and secrete GFAP

938
Q

What organisms produce large liver cysts that are hypoechoic with a calcified rim? What are these cysts called?

A

tapeworm: Echinococcus granulosus

Hydatid cysts

939
Q

How would you distinguish between anorexia nervosa with bingeing and purging and bulemia nervosa?

A

Anorexia typically presents with v. low BMI vs bulemia which tends to present with either normal or elevated BMI

940
Q

What anticancer drug inhibits topoisomerase II? What is it commonly used for? What are the side effects?

A

Etoposide, small cell lung cencer, prosate cancer, refractory testicular carcinoma

Side effects: alopecia and myelosuppression

941
Q

What is the diagnosis based on this kidney biopsy of a patient with SLE?

A

Membranous nephropathy

942
Q

What asthma therapy interacts with these cells?

A

Mast cells - cromolyn sodium prevents degranulation.

943
Q

What disorder results in assigned female appearance at birth with XY genotype and normal levels of testosterone, estrogen and LH?

A

5-alpha reductase deficiency

944
Q

What condition may cause polyhydramnios in utero? What is the appearance on X-ray? What is the associated syndrome?

A

Tracheoesophageal fistula

Gastric air bubble on x-ray

VACTERL

Vertebral abnormalities, Anal atresia, Cardiac defects, TE fistula, Renal & gu abnormalities, Limb defects

945
Q

What do you do when a patient gives a comment on your youthful appearance?

A

Acknowledge it / thank them for the compliment.

946
Q

What is the only detectable sign of HBV infection during the window period? Why?

A

HBcAb

Due to the fact that HBsAg is being bound by HBsAb, but there is not enough HBsAb remaining unbound for it to be detectable

947
Q

What does alpha-amanitin block?

A

RNA pol II and III; causing decreased heterogenous nuclear RNA which normally is processed into mRNA

948
Q

What is the immediate change in hormone concentrtion that occurs due to starting a combined OCP?

A

progesterone -> negative feedback on GnRH -> less FSH which inhibits follicular growth and reduces estrogen concentration -> no positive LH feedback, no LH surge & no ovulation

949
Q

What type of anemia is indicated by the presence of target cells?

A

Thalassemia

950
Q

What is the anemia characteristic of sickle cell disease?

A

Normocytic, increased RDW, low red cells

951
Q

What are the first two (irreversible) steps in gluconeogenesis?

A

Pyruvate to oxaloacetate via pyruvate carboxylase

oxaloacetate to phosphoenolpyruvate via PEP carboxylase

952
Q

What organ is responsible for secreting HCO3- to neutralize stomach acid?

A

Exocrine pancreas