Qbank Step 2 Flashcards
What 4 cancers cause ectopic Cushing’s syndrome?
- Small Cell Lung Ca
- Pancreatic Cancer
- Neuroendocrine tumors
- Bronchial carcinoids
erythematous papules with a central scale with a sandpaper like texture on palpation
actinic keratoses
what is trismus?
inability to open the mouth normally, seen in retropharyngeal abscess
how long is a pt at risk for strep pneumo sepsis after splenectomy?
> 30 years!!! pts should receive anti-pneumococcal, h flu, and meningococcal vaccines several weeks before operation and daily oral penicillin ppx for 3-5 years following splenectomy
palpable purpura + proteinura + hematuria?
suspect mixed cryoglobulinemia: also includes nonspecific systemic symptoms, arthralgias, hepatosplenomegaly, and hypocomplementemia
what infection is associated with mixed cryoglobulinemia?
hepatitis C
how does henoch-schonlein purpura present? (5)
- presents in childhood as:
1. palpable purpura on the buttocks
2. Abdominal pain
3. Arthralgias
4. Proteinuria
5. Hematuria - serum complement levels are normal
how do you differentiate between restrictive and obstructive lung disease on PFTs?
The FEV1/FVC ratio:
restrictive >80%
obstructive <80%
What are the criteria for making a diagnosis of polymyalgia rheumatica? (4)
- Age over 50
- Aching pain in the neck, pelvis, and shoulder lasting >1mos
- Morning stiffness lasting ?1hr
- ESR >40
tx: low dose prednisone
what disease does polymyalgia rheumatica commonly present with?
giant cell arteritis
what are some maneuvers used to treat paroxysmal supraventricular tachycardia? (3) how do they work?
- Valsalva
- carotid sinus massage
- immersion in cold water
- these increase vagal tone and decrease conduction through the AV node
what is paroxysmal supraventricular tachycardia and what is one med used to tx it?
- most common paroxysmal tachycardia in pts without structural heart defects
- heart rates between 160-220bpm
- caused by re-entry into the AV node
- Adenosine: AV nodal blocker short acting
what 4 diseases are associated with erythema nodosum?
erythema nodosum: painful subcutaneous nodules on the anterior surface of the lower legs
- Sarcoid
- TB
- Histoplasmosis
- IBD
all forms of gestational trophoblastic disease present w what 3 symptoms?
- Irregular vaginal bleeding
- Enlarged uterus
- Pelvic pain
what are some causes of pericardial effusion?
- Idiopathic (most common) following viral
- Malignancy
- Post-MI
- Uremia
- Autoimmune diseases
- Hypothyroidism
risk factors for splenic abscess?
- Infection: infective endocarditis with hematogenous spread
- Immunosuppression
- IV drug use
- Trauma
- Hemoglobinopathies
treatment of splenic abscess?
splenectomy!! or IR drainage for poor surgical candidates
why does niacin cause pruritis and flushing??
niacin-induced prostaglandin and histamine release causing peripheral vasodilatation, NOT a hypersensitivity reaction
Side effect of rifampin?
causes red to orange discoloration of body fluids including urine, saliva, sweat and tears (even soft contact lenses)
Pts with rheumatoid arthritis are at risk of developing what long term complication?
osteoporosis/osteopenia/fractures
why does sickle cell trait cause painless hematuria?
papillary ischemia: which is due to the relatively low local oxygen partial pressure
focal segmental glomerulosclerosis is associated with what?
- African Americans (more than 1/2 of nephrotic cases in AA)
- Obesity
- Heroin
- HIV
pt has celiacs but a negative IgA anti-tissue transflutaminase!?!?!? what!?!
- ppl w/ celiacs often have selective IgA deficiency as well meaning…. no IgA! so serological studies will be negative
what plasma aldosterone concentration: plasma renin activity ratio suggests primary hyperaldosteronism?
Ratio >20
with plasma aldosterone >15ng/dL
Pleural fluid glucose <60mg is usually due to what 6 causes?
- Rheumatoid pleurisy
- Complicated parapneumonic effusion or empyema
- Malignant effusion
- TB pleurisy
- Lupus pleuritis
- Esophageal rupture
Pleural glucose <30 usually due to what 2 causes?
- Empyema
2. Rheumatic Effusion
what serum compliment levels are low in poststrep glomerulonephritis?
C3 complement
what is winters formula?
PaCO2 = 1.5 (HCO3) + 8
- can be used to calculate the expected PCO2 during respiratory compensation for a primary metabolic acidosis
when should you take a pt with SBO to the OR?
when they dont improve with conservative measures or there’s signs of strangulation (fever, tachycardia, leukocytosis, metabolic acidosis)
what is Trousseau’s syndrome? 6 associated cancers?
- aka migratory superficial thrombophlebitis
- is a hypercoagulable disorder that usually presents with unexplained superficial venous thrombosis at unusual sites (arm, chest area)
- most commonly associated with visceral malignancy:
1. Pancreas
2. Lung
3. Prostate
4. Stomach
5. Colon
6. Acute leukemias
Pt complains of seeing halos around lights
think of angle closure glaucoma
what two factors increase the overall risk of vertical transmission of HCV from mom to baby?
- HIV coinfection
2. High HCV viral load
whats the risk of sexual transmission of HCV?
in a monogamous heterosexual parternship: 0.1% annually aka VERY LOW
what medications are known to cause idiopathic intracranial hypertension? (IIH)
- Growth hormone
- Tetracyclines (minocycline, doxycycline)
- Excessive vitamin A and its derivatives
treatment for idiopathic intracranial hypertension not caused by medications?
- Weightloss
2. Acetazolamide
pt has a PAINLESS corneal ulcer- what nerve is affected?
First branch of trigeminal: ophthalmic branch
- carries sensory fiberst to the scalp, forehead, upper eyelid, conjunctiva, cornea , nose and frontal sinuses
- damage to V1 results in corneal anesthesia!
DMARD: MOA & Adverse affect- Methotrexate
MOA: Purine antimetabolite SE: Hepatotoxicity Stomatitis (oral ulcers) Cytopenias Rash, alopecia bone marrow suppression pulmonary toxicity - thus give folic acid supplemetation
DMARD: MOA & SE
Leflunomide
MOA: Pyrimidine synthesis inhibitor
SE: Hepatotoxicity
Cytopenias
DMARD: MOA & SE
Hydroxychloroquine
MOA: TNF and IL-1 Suppressor
SE: Retinopathy
DMARD: MOA & SE
Sulfasalazine
MOA: TNF and IL-1 suppressor
SE: Hepatotoxicity
Stomatitis
Hemolytic anemia
DMARDs: SE (4) TNF inhibitors (adalimumab, certolizumab, etanercept, golimumab, infliximab)
- Infection
- Demyelination
- CHF
- Malignancy
treatment of pt with torsades de pointes?
magnesium sulfate + stop offending agents
what drugs cause torsades?
- TCAs
- Anti-arrhythmics: amiodarone, sotalol
- Anti-infective agents: moxifloxacin, fluconazole
a large pedunculated exophytic papule with a collarette of scale, resembles a large pyogenic granuloma or cherry angioma
- Bacillary angiomatosis: caused by bartonella henslae or quintana
- characteristic skin lesion + fever, weight loss, malaise and abdominal pain
- diagnosis made via tissue bx
- extreme caution must be taken in bx lesions bc they are prone to hemorrhage
pathophys of analgesic nephropathy
- seen in pts w several years of analgesic abuse
- chronic tubulointerstitial damace: due to renal papillary necrosis from papillary ischemia induced by analgesic-mediated vasoconstriction of medullary blood vessels
- RBCs are unchanged on UA (whereas deformed in glomerulopathy)
smudge cells and atypical lymphocytes
CLL: use flow cytometry to prove clonality
JAK2 mutations are associated with what?
myeloproliferative diseases: particularly polycythemia vera
erythematous papules with a central scale and a sandpaper like texture
actinic keratoses
treatment of frostbite to fingers?
rapid re-warming with warm water
what two liver diseases are associated with mallory hyaline bodies on liver bx?
- Alcohol liver injury
2. Wilsons disease
liver biopsy shows hepatocytes containing granules that are PAS positive and diastase resistant
Alpha-1 antitrypsin deficiency
treatment of uric acid stones?
- theyre highly soluble in alkaline urine so alkalinization of urine pH >6.5 with oral potassium bicarbonate or potassium citrate is indicted
(uric acid stones account for approx 10-15% of cases of total nephrolithiasis, seen in pts iwth unusually low urine pH levels and hyperuricosuria, they are radiolucent but can be seen on USG and CT)
what is the most common thyroid hormone pattern in sick euthyroid syndrome?
- a fall in total and free T3 levels, normal T4 and TSH, this is due to the decreased peripheral conversion of T4 to T3
- on recovery from the nonthyroid illness, pts may experience a modest, transient increase in the serum TSH levels
6month old boy has recurrent pyogenic (s pneumo and h flu) infections
think brutons agammaglobulinemia: x linked recessive
what is the defect in brutons agammaglobulinemia?
defect in tyrosine kinase in B cells
what are 3 neurologic complications of measles?
- Encephalitis (within days)
- Acute disseminated encephalomyelitis (within weeks)
- subacute sclerosing panencephalitis (within years)
3yo boy has recurrent staph infections & aspergillus
think chronic granulomatous disease: mutation causes loss or inactivation of the NADPH oxidase responsible for oxidation, patients experience recurrent infections by catalase expressing organisms
gram stain = neutrophils filled wth bacteria
C3 deficiency predisposes kids to what?
recurrent infections with encapsulated bacteria beginning shortly after birth
kid w recurrent fungal and viral infections
think DiGeorge syndrome
steps for management of newborn who doesnt pass meconium within first 24 hours?
- KUB: to look for pneumoperitoneum from perforated bowel
- Contrast enema: to assess for microcolon (meconium ileus- gastrografin can break up meconium and is thus therapeutic) or a transition zone w dilated megacolon (hirschsprung disease)
- If meconium ileus: get sweat chloride test, if hirschsprung: get rectal biopsy
how does maternal diabetes lead to Resp distress syndrome in infants?
- maternal diabetes delays the maturation of surfactant production in the lungs
- fetal hyperinsulinism antagonizes the actions of cortisol and may delay the lung maturation process
infants with laryngomalacia are at risk of waht?
GERD- which can aggravate airway collapse
Eerb duchenne palsy involves what branches?
C5-C7
2 known GI complications of HSP in kids?
GI Hemorrhage
Intussusception
risk factors for cholecystitis in children? (3)
- Sickle cell anemia
- Hereditary spherocytosis
- Obesity
what EKG finding is a minor Jones criteria for rheumatic fever?
proloned PR interval
most common complication of HUS?
renal damage
classic triad of congenital rubella syndrome?
- Deafness
- Cataracts
- Cardiac defects
how do you confirm the diagnosis of Lyme arthritis?
ELISA and western blot testing
what is reactive arthritis?
- acute and asymmetric oligoarthritis that occurs 1-4 weeks after urethritis or diarrheal infection
most common cause of bacteremia in sickle cell patients?
strep pneumo
when is a voiding cystoureterogram indicated in peds patients?
- Patient is under 10 years of age
- Male
- Prepubertal non-sexually active female
medulloblastoma arises from where?
cerebellar vermis
what is associated with breathholding spells??
Iron Deficiency Anemia
what 3 factors increase the risk of iron deficiency anemia in infants?
- Maternal IDA
- Prematurity
- Early introduction of cow’s milk before age 12 months
when should you supplement vitamin B12 in infants?
those exclusively breastfed by strict vegetarian mothers
difference in timing of transient synovitis and legg-calve-perthes disease?
transient synovitis: 1 month
symptoms of riboflavin deficiency? (vit b2)
- cheilosis
- glossitis
- seborrheic dermatitis (often affecting the genital areas)
- Pharyngitis
- edema and/or erythema of the mouth
Differential for T wave inversions: (5)
- MI
- Myocarditis
- Old pericarditis
- Myocardial contusion
- Digoxin toxicity
the most common primary bone tumor affecting children and young adults?
osteosarcoma
most common cause of congenital hypothyroidism in the US?
thyroid dysgenesis
4 contraindications to the rotavirus?
- Anaphylaxis to ingredients
- Hx of intussusception
- Hx of uncorrected congenital malformation of GI like Meckels
- SCID
doxycycline is contraindicated in what 2 patient populations?
- Children <8 years
- Pregnant women
- use oral amoxicillin or cefuroxime instead
when do you use IV ceftriaxone in Lyme disease?
reserved for Lyme meningitis and heart block (manifestations of early disseminated lyme disease)
what is the most common childhood cancer?
Acute Lymphoblastic Leukemia
what are the 3 most common cardiovascular abnormalities seen in Turner’s syndrome?
- Bicuspid aortic valve
- Coarctation of the aorta
- Aortic root dilation
treatment of kawasaki’s?
ASA plus IVIg
what are the HLA-B27 associations?
PAIR: Psoriasis Ankylosing spondylitis IBD Reiter's syndrome
screening recommendations for AAA?
any many 65-75 who have ever smoked
4 drug classes that are known to cause esophagitis?
- Tetracyclines
- ASA (and many NSAIDs)
- Bisphosphonates
- Others: Potassium chloride, quinidine, Iron
treatment of choice for uremic pericarditis?
hemodialysis!
Indications for Hemodialysis (6)
- Refractory hyperkalemia
- Volume overload unresponsive to diuretics
- Refractory metabolic acidosis (pH <7.2)
- Uremic pericarditis
- Uremic encephalopathy or neuropathy
- Coagulopathy due to renal failure
electron microscopy findings include alternating areas of thinned and thickened capillary loops with splitting of the GBM
alport’s syndrome
what is the most common primary intracardiac tumor and where are they usually found?
atrial myxomas: found in the L atrium
what antiretroviral drug is known to cause crystal-induced nephropathy?
Idinavir (protease inhibitor)
thus monitor with UA and serum Cr levels q3-4months
Name the life threatening ART side effect:
Didanosine
pancreatitis
Life trheatening side ART effect:
Abacavir
Hypersensitivity syndrome (rash -> anaphylaxis upon next exposure)
Life threatening ART side effect:
NRTIs
lactic acidosis
Life threatening ART side effect: NNRTIs
SJS
Life threatening ART side effect: Nevirapine
liver failure
when do u give itraconazole for histo ppx in HIV pts?
when CD4 count is less than 100 and they live in areas endemic for histoplasmosis
hereditary spherocytosis is disorder of what?
autosomal dominant disorder of spectrin- the protein that provides scaffolding for RBCs
treatment of hereditary spherocytosis?
folate supplementation and splenectomy
Diagnostic criteria for ATN? (4)
- Urine osmolality 300-350 (but never 20
- FeNa >2%
- BUN:Cr <20:1
Name the association:
- Muddy brown granular casts
- RBC casts
- WBC casts
- Fatty casts
- Broad and waxy casts
- Muddy brown: ATN
- RBC: glomerulonephritis
- WBC: Interstitial nephritis and pyelonephritis
- Fatty casts: nephrotic syndrome
- Broad and waxy: chronic renal failure
what is MEsna used for?
to prevent hemorrhagic cystitis caused by certain chemotherapeutic agents (cyclophosphamide)
3 phases of Trichinellosis? (from eating undercooked pork)
- Initial: larvae invade the intestinal wall causing abdominal pain, N/V, diarrhea
- Second: hypersensitivity as larvae migrate causing splinter hemorrhages, conjunctival and retinal hemorrhages, chemosis
- Third: larvae enter skeletal muscle, muscle pain tenderness, swelling & weakness
- blood count usually shows eosinophilia
triad of trichinella?
- Periorbital edema
- Myositis
- Eosinophilia
2 types of autoimmune hemolytic anemia?
- Warm agglutinin: more common, due to autoimmune disease that is tx with steroids, rituximab (CD20 ab), splenectomy, or immunosuppression
- COld agglutinin: may be due to infections or autoimmune disease causing intravascular hemolysis, tx is supportive care (warming body) and RBC transfusions
Cyclosporine and tacrolimus: MOA?
calcineurin inhibitors
Major side effects of cyclosporine? Tacrolimus?
Cyclosporine:
- Nephrotoxicity
- Hyperkalemia
- HTN
- Gum hypertrophy
- Hirsutism
- tremor
* Tacrolimus has the same EXCEPT for hirsutism and gum hypertrophy
Major toxicities of azathioprine? 3
- Dose related diarrhea
- Leukopenia
- Hepatotoxicity
Major toxicity of mycophenolate?
bone marrow suppression
treatment of myasthenia crisis?
endotracheal intubation and withdrawal of anticholinesterases for several days
what are the 5 major criteria of rheumatic fever?
- Polyarthritis
- Chorea
- Carditis
- Subcutaneous nodules
- Erythema marginatum
treatment of rheumatic fever?
penicillin G
infantile hypertrophic pyloric stenosis is most common in what pts?
first born males age 3-5 weeks
what are the risk factors for jejunal/ileal atresia in infants?
- poor fetal gut perfusion from maternal use of vasoconstricive medications or drugs ie cocaine & tobacco
what is often the first symptom of autistic disorder?
lack of social smile
tx of choice for impetigo?
topical mupirocin
what are the indications for imaging prior to LP in infants and children?
- Hx of hydrocephalus
- Hx of head trauma
- Hx of VP shunt or neurosurg
- Comatose
- Focal neurological findings
birth weight should be regained by
10-14 days
How do you diagnose tinea corporis?
with a skin scraping and potassium hydroxide examination, or clinically
babies born with a sacral dimple or tuft of hair should be screened for what and how?
for occult spinal bifida with a lumbosacral ultrasound (if this is abnormal then perform a MRI of spine
treatment of choice for developmental dysplasia of hip in infant <6 months?
Pavlik hip harness
features of vascular ring in children
- Presents before 1 year
- Persistent stridor that improves with neck extension
- Associated with cardiac abnormalities
- result of abnormal development of the aortic arch causing tracheal, bronchial or esophageal compression
inheritance of myotonic muscular dystrophy?
autosomal dominant
Intraventricular hemorrhage is common in which neonates?
born <1500g
- thus screening w serial head USs is necessary
what is the most common predisposing factor for orbital cellulitis?
bacterial sinusitis
MOA of ethosuximide?
affects the thalamic neurons by woking against calcium currents
how does vitamin A help reduce mortality in pt w measles??
it helps the GI and respiratory epithelium regenerate and enhances the immune system
how do you diagnose choanal atresia?
first: try passing a catheter through nose 3-4cm into oropharynx
then: CT scan with intranasal contrast, which shows a narrowing at the level of the pterygoid plate
what two immunizations are known to cause febrile seizures?
- DTaP
2. MMR
what is the Guthrie urine test?
a qualitative (coloration) test that detects the presence of metabolic products of phenylalanine in the urine - used to diagnose PKU, can also use blood phenylalanine levels
heart defects associated with digeorge?
- Trucus arteriousus
- TOF
- Interrupted aortic arch
- Septal defects
pathology of retinoblastoma?
inactivation of the Rb suppressor gene: can be familial or sporadic
- failure to treat early may lead to death from liver and brain mets
what is werdnig-Hoffman syndrome?
autosomal recessive disorder that involves degeneration of the anterior horn cells and cranial nerve motor nuclei
aka floppy baby syndrome
what is the most common extracranial solid tumor of childhood?
neuroblastoma
neuroblastoma arises from what embryonic origin?
neural crest cells: amplification of n-myc proto-oncogene and hyperdiploidy
wilms tumor arises from what embryonic origin?
metanephros: embryologic precursor of the renal parenchyma
mesonephros gives rise to the what?
- Seminal vesicles
- Epididymis
- Ejaculatory ducts
- Ductus deferens
paramesonephron gives rise to what?
- Fallopian tubes
- Uterus
- Part of the vagina
disregulation of imprinted gene expression in chromosome 11p15
- macroglossia, rapid growth, hemihyperplasia, umbilical hernia or omphalocele
Beckwith-Wiedemann syndrome
deletion of paternal copy of 15q11-q13
Prader Willi syndrome: sporadic disorder due to maternal uniparental disomy (inheriting both copies on chrom 15 from mother)
paternal uniparental disomy- deletion of maternal copy of chromosome 15q11-q13
angelman syndrome
pts w galactosemia are at an increased risk of what kind of sepsis?
e coli neonatal sepsis
bullous type impetigo is caused by what organism?
staph!
the other type is vesiculo-pustulo which i think is from strep
small erythematous patch on a kids cheek that is raised, sharply demarcated with advancing pargins
erysipelas: red, indurated, tense and shiny plaque
- can have lymphatic involvement
- usually due to Streptococci, penicillin is DOC
most common heart defects in downs from most common
- Complete Atrioventricular septal defect (endocardial cushion) = heart failure at 6 weeks
- VSD
- ASD
what is the most common cause of secondary hypertension in children?
fibromuscular dysplasia: most commonly affects the R renal aa, angiography shows a string of beads pattern to the renal aa
radiographic evidence of intra-cranial calcifications that resemble a tramline + seizures
sturge-weber syndrome
most common presenting symptom of craniopharyngioma in children vs adults
Children: retarded growth due to growth hormone and thyroid function
Adults: sexual dysfunction/amenorrhea
treatment for acute migraine HA?
IV Antiemetics (chlorpromazine, prochlorperazine, metoclopramide)
- can add NSAIDs or triptans too
- propanolol and amitriptyline are used for migraine prophylaxis
How does ABPA (allergic bronchopulmonary aspergillosis) usually present?
its a hypersensitivity reaction to Aspergillus colonization of the bronchi
- occurs most commonly in patients with athma or CF
- presents with:
1. Fever
2. Malaise
3. Productive cough
4. Eosinophilia
5. Hemoptysis
what are the causes of atypical pneumonia? (5)
- Mycoplasma pneumoniae (most common in ambulatory setting)
- Chlamydia pneumoniae
- Legionella
- Coxiella
- Influenza
what cause of atypical pneumonia is assocaited with a skin rash?
mycoplasma pneumo:
erythema multiforme: dusky red target shaped skin lesions over all four extremities
what is cerebral salt-wasting syndrome?
may occur in patients with subarachnoid hemorrhage
1. Inappropriate secretion of vasopressin -> water retention
2. Increased secretion of atrial/brain natriuretic peptide which causes cerebral salt wasting
- can also see SIADH
= hyponatremia
treatment of pagets disease?
tx symptomatic pts with bisphosphonates
what drug can cause a maculopapular rash with EBV?
amoxicillin (and other antibiotics)
what marker is relatively specific for hairy cell leukemia?
CD11c
- will also be tartrate-resistant acid phosphatase (TRAP) stain
neurocystericercosis is caused by what?
eating the larval stage of the pork tapeworm Taenia solium (eat eggs excreted by another person)
hyatid cysts are caused by what and seen in what pts?
- caused by echinococcus species and usually seen in the liver and lungs
- more common in sheep breeders
what type of hemolytic anemia do you see in a malignant lymphoproliferative disorder?
warm autoimmune type- caused by anti-red blood cell IgG antibodies,
tx: prednisone, if that doesnt work then splenectomy
why do people with chronic renal failure have abnormal hemostasis? tx?
due to uremic coagulopathy: several uremic toxins cause platelet dysfunction- ie guanidinosuccinic acid
- PT, PTT and TT are normal, BT is prolonged
tx: Desmopressin, cryoprecipitate and conjugated estrogens
what is the underlying pathology of parkinsons?
degeneration of neurons in the substantia nigra- leading to decreased dopaminergic activity and increased cholinergic activity
the risk of hemophilic arthropathy can be significantly reduced by what?
prophylactic treatment with factor concetrates
treatment of choice in kids with constipation?
Oral laxatives: polyethylene glycol and mineral oral
direct head injury followed by a lucid interval then rapid neurologic deterioration w HA vomiting seizures, confusion and lethargy
epidural hematoma: injury to meningeal blood vessels, do not cross suture lines
- dx = CT scan
clinical features that necessitate an emergent craniotomy in epidural hematomas? 5
- GCS <8
- Signs of increased ICP
- Pupillary abnormalities
- Hemiparesis
- Cerebellar signs
whats Friedreich taxia?
most common type of spinocerebellar ataxias
- Neurologic sx: ataxia, dysarthria
- Skeletal: scoliosis, feet deformities
- Cardiac: concentric hypertrophic cardiomyopathy
- most common cause of death are cardiomyopathy and resp complications
- lifespan >20 years
what is the most common pathogenic organism in young CF children in the setting of concurrent influenza infection?
Staph aureus
- after the age of 20, pseudomonas becomes the most common in CF pts
kid w downs syndrome presents with upper motor neuron findings?
- Think atlantoaxial instability
what drugs can cause a serum sickness like reaction and in what setting?
- Amoxicillin
- Penicillin
- Cefaclor
- in the setting of a viral illness
sx: fever, uticarial rash, polyarthralgia and lymphadenopathy
what is the most common complications of supracondylar fractures?
entrapment of the brachial artery
classic triad of congenital rubella?
- Leukocoria (white papillary reflex) from cataracts
- Murmur of PDA
- Hearing loss
how does congenital CMV and rubella differ?
Congenital rubella (triad of leukocoria, PDA< hearing loss) Congenital CMV: deafness, purpura, hepatospneomegaly, sensorineural hearing loss
- In CMV, the deafness is typically unilateral, blindness is usually due to chorioretinitis, and the heart is unaffected
injury in nurse maids elbow??
radial head subluxation: child typically keeps hand in pronated position and refuses attempted forearm supination
low birth weight, closed fists with the index overlapping the 3rd and the 5th overlapping the 4th, microcephaly, prominant occiput, micgrognathia, abduction, short sternum, cardiac and renal malformations, and mental retardation
Edwards syndrome: trisomy 18
whats the actual name of the pinworm?
tx?
enterobius vermicularis
tx: albendazole or mebendazole, but do NOT use in pregnant patients
how is HSP different from other causes of purpura?
it has a normal platelet count
first line treatment for pertussis?
macrolide antibiotic: erythromycin, azithromycin, or clarithromycin
- must treat all family and close contacts regardless of immunization status
3 syndromes associated wtih Wilms tumor? (nephroblastoma)
- WAGR: wilms, aniridia, GU anomalies, intellectual disability
- Beckwith-Wiedemann syndrome
- Denys-Drash syndrome
epidemiology of neuroblastoma? how does it differ from Wilms?
- third most common pediatric cancer (after leukemia and brain), but most common cancer in FIRST year of life
- presents as an abdominal mass that CROSSES the midline whereas Wilms does NOT cross the midline
whats the primary pathophysiologic cause of throbocytopenia in patients with WAS?
decreased platelet production
what are the EKG findings of WPW? (3)
- Shortened PR interval
- Slurred initial portion of the QRS complex (delta wave)
- Widened QRS
treatment of reyes syndrome?
administration of glucose with FFP and mannitol to decrease cerebral edema
what is Jervell-Lange-Nielson syndrome?
one of the congenital QT prolongation syndromes
- autosomal recessive disease characterized by:
1. congenital deafness
2. QT prolongation
tx= propanolol
what should be used as IV fluid resuscitation in children?
isotonic saline or LR