Test 1 Flashcards

1
Q

Guillain-Barre syndrome is often associated with ____ infection. This bacteria is a Gram-__ organism with a characteristic curved-___ shape. Diagnosis is confirmed with culture, and further testing will be ____ for catalase and oxidase

A

Campylobacter jejuni/ negative/ rod/ positive

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2
Q

A Gram-negative, oxidase-negative rod which does not ferment lactose (white colonies on MacConkey agar) or produce hydrogen sulfide (no blackening on TSI) is ____, a extremely virulent bacteria. It invades via the ….. cells found in the Peyer patches of the small intestine, spreading between cells by actin ……

A

Shigella/ M/ rockets

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3
Q

Liver abscess and toxic megacolon result from …… infection

A

Entamoeba histolytica

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4
Q

Meningitis is a complication of invasive ……., caused by ……. Listeriosis causes a self-limiting diarrheal illness in healthy individuals, but can also manifest as neonatal or pediatric …… and …… Symptoms in pregnant women may also include nausea, vomiting, diarrhea, and fever. It does not cause …… diarrhea. Listeria is a Gram-……, ….-shaped bacteria with ….. motility under light microscopy.

A

listeriosis/ Listeria monocytogenes/ meningitis/ sepsis/ bloody/ positive/ rod/ tumbling

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5
Q

Both _____ and _____ are gram ⊝rods, non-lactose fermenters, oxidase ⊝, and can invade the GI tract via M cells of Peyer patches

A

Salmonella/ Shigella

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6
Q

Li-Fraumeni syndrome is characterized by an autosomal ____ mutation in ____ that is associated with multiple malignancies at an early age. Commonly-associated malignancies can be remembered with the mnemonic __ cancer syndrome: ____, ____, _____, and ____ cancers. In Li-Fraumeni syndrome, one abnormal copy of ____ is inherited, leading to heterozygosity of p53. If the other copy becomes mutated or deleted, there is loss of function of p53. While loss of function of one copy increases cancer risk, both alleles must be lost for expression of the disease.

A

dominant/ P53/ SBLA/ Sarcoma/ Breast/ Leukemia/ Adrenal gland/ P53

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7
Q

In any adult with more than _____ cases of consolidated pneumonia in 1 year, or more than ___ upper respiratory infections (URIs) in 1 year, the physician should consider an immunodeficiency. _____ deficiency is the most common immunodeficiency. Although most patients with this deficiency are asymptomatic, patients are at risk for the development of anaphylactic reactions following ____ or administration of intravenous _____.
IgA is involved in preventing invasion by pathogenic organisms and has a crucial role in maintaining the homeostatic balance between the host and the commensal microbiota. Thus, patients with selective IgA deficiency are particularly susceptible to ____ infections, especially ____.

A

two/ four/ Selective IgA/ blood transfusions/ immunoglobulin (IVIG)/ gastrointestinal/ giardiasis

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8
Q

Risk factors for N. meningitidis infections include living in ____ spaces, or having a history of ____ procedure.

A

close contact/ splenectomy

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9
Q

Positive Stool guaiac test result means …….

A

blood in stools

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10
Q

Celiac disease is an autoimmune-mediated intolerance of ….., which is a gluten protein found in wheat.

A

gliadin

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11
Q

Hypertrophic cardiomyopathy manifests with an …. gallop and ……. murmur along the left sternal border. It can be treated with ….. or with non-dihydropyridine ……..

A

S4/ systolic/ β-blockers/ calcium-channel blockers

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12
Q

Septic arthritis is a finding in patients with ____ infection. It presents with fever, migratory joint pain, and synovial inflammation.

A

Neisseria gonorrhoeae

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13
Q

Doxorubicin is commonly used in the initial stage of _____ treatment. It inhibits DNA synthesis through the generation of free radicals that cause strand breaks. It also has the ability to intercalate (insert) between DNA base pairs, and therefore acts during ____ phases of the cell cycle.

A

acute lymphoblastic leukemia/ multiple

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14
Q

___ and _____ are plant alkaloid derivatives that act on cells specifically during the M phase of the cell cycle. They bind to tubulin and block polymerization of microtubules, preventing mitotic spindle assembly and promoting cell cycle arrest in M phase.

A

Vincristine/ vinblastine

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15
Q

Broad-based budding yeast refers to ____. It is found in wooded areas east of the _____ River.
Budding yeast with pseudohyphae refers to ____, which can cause thrush, vulvovaginitis, and numerous other mucocutaneous infections. Mold with hyphae that branch at 45-degree angles refers to ____, which more commonly infects individuals with underlying pulmonary disease or those working in construction (due to inhalation exposure).
Small intracellular yeast refers to ____, a fungus found in the Mississippi and Ohio River valleys.

A

Blastomyces/ Mississippi/ Candida albicans/ Aspergillus fumigatus/ Histoplasma

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16
Q

Lead inhibits ______, preventing ____ formation. Lead also disrupts the incorporation by ___ of iron into ____, which is the final step in heme synthesis. Inhibition of either of these steps results in ineffective heme synthesis and subsequent __ (hemoglobin-poor) anemia.

A

δ-aminolevulinic acid (ALA) dehydratase/ porphobilinogen/ ferrochelatase/ protoporphyrin IX/ microcytic

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17
Q

Mixed metabolic acidosis and respiratory alkalosis is associated with ____ toxicity, as the acidic metabolites trigger the brain to hyperventilate and blow off the excess acid in the form of CO2.

A

aspirin

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18
Q

Pain over the anatomic snuff box is pathognomonic for _____ fracture. This fracture is usually due from a fall on an _____ hand. It presents with persistent pain the anatomical snuff box. It may take up to ______ or more for the fracture to be seen on radiology imaging. The scaphoid bone has tenuous blood supply fed by retrograde flow, so it can be vulnerable to avascular necrosis after fracture

A

scaphoid/ outstretched/ 3 weeks

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19
Q

A patient with a prescription for tetracycline antibiotic for acne can use Demeclocycline, a tetracycline that impairs the action of _____ at its receptor, causing ______, which manifests as urinary frequency and polydipsia. A water deprivation test would reveal inappropriately _____ urine in the context of decreased water intake as a result of nonfunctional ADH.

A

antidiuretic hormone (ADH)/ nephrogenic diabetes insipidus/ dilute

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20
Q

______ are common, benign central nervous system tumors that arise from arachnoid cells outside of the brain parenchyma, and they may have a dural attachment.

A

Meningiomas

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21
Q

_____ is the most common primary brain tumor in adults and is typically found within the cerebral hemisphere. It can cross the corpus callosum, forming a “_____.” Histologic examination reveals pleomorphic tumor cells and central areas of necrosis and hemorrhage. Prognosis is extremely poor.

A

Glioblastoma multiforme/ butterfly glioma

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22
Q

Hemangioblastomas are more common in ____ and are often located in the _____. The cells tend to be “foamy,” and the tumors display a high degree of ____. These tumors are associated with ____ syndrome

A

children/ cerebellum/ vascularity/ von Hippel-Lindau

23
Q

Pathology specimens of ____ reveal “fried egg” cells. These cells have round nuclei amidst a halo of clear cytoplasm. It is a ____ brain tumors found in the cerebral hemispheres. They tend to have areas of calcification that can be detected radiographically.

A

oligodendrogliomas/ benign

24
Q

Schwannoma is the third most common primary brain tumor. It has a Schwann cell origin and is often localized to ____. A schwannoma is usually found at the cerebellopontine angle. Histologically, schwannomas are characterized by densely cellular ____ areas and loosely cellular ______ areas. Both areas are composed of spindle-shaped tumor cells, which are _____ positive.

A

cranial nerve VIII/ Antoni A/ Antoni B/ S-100

25
Q

The most common genetic condition responsible for SCID is a mutation of the _____, shared by the receptors for ___, ____, ___, ____, ____ and ___. Since this protein is encoded on the ___ chromosome, this variant of SCID is __-linked, which makes it more common in ____. These patients account for approximately 50% of all patients with SCID. All other causes of SCID are ____, and thus equally present in females and males. _____ is one of the more common autosomal recessive genetic defects in SCID, which causes T, B, and natural killer cells to dysfunction.

A

common γ chain of the interleukin (IL) receptors/ IL-2/ IL-4/ IL-7/ IL-9/ IL-15/ IL-21/ X/ X/ males/ autosomal recessive/ Adenosine deaminase deficiency

26
Q

Bilateral lesions of the amygdala cause ____ syndrome, which is characterized by ____, ____, and _____. Hyperorality means placing inappropriate objects into one’s mouth. This may be caused by _____.

A

Klüver-Bucy/ hyperorality/ hypersexuality/ behavioral disinhibition/ herpes encephalitis

27
Q

Gaucher disease is an ____ condition characterized by the deficiency of the lysosomal enzyme ____, leading to the accumulation of _____ in the reticuloendothelial system and causing organomegaly and infiltration of bone marrow. These patients can present at __ age with ____, ___ pain, ____, ____, and fatigue. More than 50% have bony changes seen on radiograph, most commonly manifesting as abnormal cortex of the distal femur described as having an “_____” appearance.

A

autosomal recessive/ β-glucocerebrosidase/ glucocerebroside/ any/ organomegaly/ bone/ anemia/ thrombocytopenia/ Erlenmeyer flask

28
Q

Tay-Sachs disease, an ____ condition common in Ashkenazi Jews, is characterized by the deficiency of the lysosomal enzyme ____, leading to the accumulation of ____ within cells. These patients present around 4 years of age with decreased ____, increased ____, ____, _____, ____, and _____. Neurologic degeneration and death occur within several years of diagnosis.

A

autosomal recessive/ hexosaminidase A/ gangliosides/ eye contact/ startle/ macrocephaly/ seizures/ ataxia/ cherry-red spots on the macula

29
Q

____ disease, also called hepatolenticular degeneration, is caused by an ____ mutation in the hepatocyte ___-transporting ATPase (___ gene; chromosome 13) gene. This gene prevents excretion of copper from the body. Thus, there is a decrease in copper incorporation into apoceruloplasmin, and a decrease of copper excretion into the bile, causing ____ in serum ceruloplasmin. The Parkinsonian-like movement are a direct result of copper accumulation in the ____. Lab findings include ____ and possible indications of renal disease. Treatment includes chelation with either ___, ____, or oral __.

A

Wilson/ autosomal recessive/ copper/ ATP7B/ decrease/ basal ganglia/ hemolytic anemia/ penicillamine/ trientine/ zinc

30
Q

The maintenance dose is calculated as: ______. Drugs administered intravenously have a bioavailability of __.

A

Target plasma concentration (Cp) × Drug clearance [CL] × Dosage interval [τ])/ Bioavailability [F]; 1

31
Q

India ink is a negative stain that can help to identify some ___ organisms with a gelatinous capsule, which do not pick up other more common stains. India ink is used to identify ___ species

A

fungal/ cryptococcal

32
Q

Drugs that can induce folate deficiency are ____, ____, and ____

A

phenytoin/ sulfonamides/ methotrexate

33
Q

The Toll-like receptor 4 recognises ……

A

LPS

34
Q

The Toll-like receptor 2 recognises ……

A

Peptidoglycan

35
Q

The autosomal dominant diseases are: ______ (type 2A), ______, _______, ______ type 1 and ______

A

Familial hypercholesterolemia/ Huntington disease/ Neurofibromatosis/ Marfan syndrome/ acute intermittent porphyria

36
Q

The autosomal recessive diseases are: ______, ______, _______, ______ and ______

A

sickle cell anaemia/ cystic fibrosis/ phenylketonuria (PKU)/ Tay Sachs disease

37
Q

The autosomal dominant diseases are: ______ (type 2A), ______, _______, ______ type 1 and ______

A

Familial hypercholesterolemia/ Huntington disease/ Neurofibromatosis/ Marfan syndrome/ acute intermittent porphyria

38
Q

The autosomal recessive diseases are: ______, ______, _______, ______ and ______

A

sickle cell anaemia/ cystic fibrosis/ phenylketonuria (PKU)/ Tay Sachs disease

39
Q

NF-1 gene is a …… gene, and when mutated give rise to …….

A

tumor supressor/ Neurofibromatosis type 1

40
Q

The X-linked dominant diseases are: ______ and ______

A

Fragile X syndorme/ Hypophosophatemic rickets (vitamin D resistant ricket)

41
Q

NF-1 gene is a …… gene, and when mutated give rise to …….

A

tumor supressor/ Neurofibromatosis type 1

42
Q

Rb gene is a …… gene, and when mutated give rise to …….

A

tumor supressor/ retinoblastoma

43
Q

Diseases that can result from mRNA splicing defect are: ….., ……., ……., …… and …….

A

B-talassemia/ LES/ Tay Sachs/ Gaucher/ Marfan

44
Q

INF alpha is used in the treatment of __, ___, ____, ____ and _____

A

Hepatitis B/ Hepatitis C/ CML/ hairy B cell leukemia/ kaposi sarcoma

45
Q

IFN Beta is used to treat ____

A

Multiple Sclerosis

46
Q

Blood tests done to detect Down syndrome in uterus are: ____, _____ and _____

A

AFP/ estriol/ ach

47
Q

Microdeletions of chunks of chromosomes cause the following pathologies: _____ (chromosome __), _____ (chromosome __), _____ (chromosome __), and _____ (chromosome __),

A

Cri-Du-Chat/ 5/ alpha-thalassemia/ 16/ Di George/ 22/ William Syndrome/ 7

48
Q

Blood tests done to detect Down syndrome in uterus are: ____, _____ and _____

A

AFP/ estriol/ ach

49
Q

The cytokine ___ stimulate the isotope switch to IgG, while the cytokines __ and __ stimulate the isotope switch to IgE, and the cytokines __ and __ stimulate the isotope switch to IgA

A

IFN gamma/ IL 4/ IL 13/ IL 5/ TGF Beta

50
Q

IgM has ___ affinity and ____ avidity compared to IgG

A

lower/ higher (related to valency)

51
Q

Fibrinoid necrosis is typically seen in ____ and ____

A

acute immune diseases/ malignant hypertension

52
Q

Dry gangrene has ____ necrosis, wet gangrene has ____ necrosis

A

coagulative/ liquefactive

53
Q

Systolic interval is a marker of _____, while diastolic interval is a marker of _____. Decrease systolic interval _____ (increase or decrease) in ______. Ejection fraction is a marker of _____.

A

contractility/ heart rate/ increase/ contractility/ contractility