RAPID REVIEW CLASSIC LABS Flashcards
(106 cards)
1
Q
LOW AFP in amniotic fluid/maternal serum
A
Down syndrome, Edwards syndrome
2
Q
Large granules in phagocytes, immunodeficiency
A
Chédiak-Higashi disease (congenital failure of phagolysosome formation)
3
Q
Recurrent infections, eczema, thrombocytopenia
A
Recurrent infections, eczema, thrombocytopenia
4
Q
Optochin sensitivity
A
Sensitive: S pneumoniae; resistant: viridans streptococci (S mutans, S sanguis)
5
Q
Novobiocin response
A
Sensitive: S epidermidis; resistant: S saprophyticus
6
Q
Bacitracin response
A
Sensitive: S pyogenes (group A); resistant: S agalactiae (group B)
7
Q
Streptococcus bovis bacteremia
A
Colon cancer
8
Q
Branching gram ⊕ rods with sulfur granules
A
Actinomyces israelii
9
Q
Hilar lymphadenopathy, peripheral granulomatous lesion in middle or lower lung lobes (can calcify)
A
Ghon complex (1° TB: Mycobacterium bacilli)
10
Q
“Thumb sign” on lateral neck x-ray
A
Epiglottitis (Haemophilus influenzae)
11
Q
Bacteria-covered vaginal epithelial cells
A
“Clue cells” (Gardnerella vaginalis)
12
Q
Cardiomegaly with apical atrophy
A
Chagas disease (Trypanosoma cruzi)
13
Q
Atypical lymphocytes
A
EBV
14
Q
Enlarged cells with intranuclear inclusion bodies
A
“Owl eye” appearance of CMV
15
Q
Heterophile antibodies
A
Infectious mononucleosis (EBV)
16
Q
Intranuclear eosinophilic droplet-like bodies
A
Cowdry type A bodies (HSV or VZV)
17
Q
Eosinophilic globule in liver
A
Councilman body (viral hepatitis, yellow fever), represents hepatocyte undergoing apoptosis
18
Q
“Steeple” sign on frontal CXR
A
Croup (parainfluenza virus)
19
Q
Eosinophilic inclusion bodies in cytoplasm of hippocampal and cerebellar neurons
A
Negri bodies of rabies
20
Q
Ring-enhancing brain lesion on CT/MRI in AIDS
A
Toxoplasma gondii, CNS lymphoma
21
Q
Psammoma bodies
A
Meningiomas, papillary thyroid carcinoma, mesothelioma, papillary serous carcinoma of the endometrium and ovary
22
Q
“Delta wave” on ECG, short PR interval, supraventricular tachycardia
A
Wolff-Parkinson-White syndrome (Bundle of Kent bypasses AV node)
23
Q
“Boot-shaped” heart on x-ray
A
Tetralogy of Fallot (due to RVH)
24
Q
Rib notching (inferior surface, on x-ray)
A
Coarctation of the aorta
25
Heart nodules (granulomatous)
Aschoff bodies (rheumatic fever)
26
Electrical alternans (alternating amplitude on ECG)
Cardiac tamponade
27
Antineutrophil cytoplasmic antibodies (ANCAs)
Microscopic polyangiitis and eosinophilic granulomatosis with polyangiitis (MPO-ANCA/p-ANCA);
granulomatosis with polyangiitis (Wegener; PR3- ANCA/c-ANCA); primary sclerosing cholangitis (MPO- ANCA/p-ANCA)
28
Hypertension, hypokalemia, metabolic alkalosis
1° hyperaldosteronism (Conn syndrome)
29
Enlarged thyroid cells with ground-glass nuclei with central clearing
“Orphan Annie” eyes nuclei (papillary carcinoma of the thyroid)
30
Mucin-filled cell with peripheral nucleus
“Signet ring” (gastric carcinoma)
31
Anti-transglutaminase/anti-gliadin/anti-endomysial antibodies
Celiac disease (diarrhea, weight loss)
32
Narrowing of bowel lumen on barium x-ray
“String sign” (Crohn disease)
33
“Lead pipe” appearance of colon on abdominal imaging
Ulcerative colitis (loss of haustra)
34
Thousands of polyps on colonoscopy
Familial adenomatous polyposis (autosomal dominant, mutation of APC gene)
35
“Apple core” lesion on barium enema
x-ray Colorectal cancer (usually left-sided)
36
Eosinophilic cytoplasmic inclusion in liver cell
Mallory body (alcoholic liver disease)
37
Triglyceride accumulation in liver cell vacuoles
Fatty liver disease (alcoholic or metabolic syndrome)
38
“Nutmeg” appearance of liver
Chronic passive congestion of liver due to right heart failure or Budd-Chiari syndrome
39
Antimitochondrial antibodies (AMAs)
1° biliary cholangitis (female, cholestasis, portal hypertension)
40
Low serum ceruloplasmin
Wilson disease (hepatolenticular degeneration; Kayser- Fleischer rings due to copper accumulation)
41
Migratory thrombophlebitis (leading to migrating DVTs and vasculitis)
Trousseau syndrome (adenocarcinoma of pancreas of pancreas or lung)
42
Basophilic nuclear remnants in RBCs
Howell-Jolly bodies (due to splenectomy or nonfunctional spleen)
43
Basophilic stippling of RBCs
Lead poisoning or sideroblastic anemia
44
Hypochromic, microcytic anemia
Iron deficiency anemia, lead poisoning, thalassemia (fetal , hemoglobin sometimes present)
45
“Hair on end” (“Crew-cut”) appearance on x-ray
β-thalassemia, sickle cell disease (marrow expansion)
46
Hypersegmented neutrophils
Megaloblastic anemia (B12 deficiency: neurologic symptoms; folate deficiency: no neurologic symptoms)
47
Antiplatelet antibodies
Idiopathic thrombocytopenic purpura
48
High level of d-dimers
DVT, PE, DIC
49
Giant B cells with bilobed nuclei with prominent (“owl’s eye”)
Reed-Sternberg cells (Hodgkin lymphoma) inclusions
50
Sheets of medium-sized lymphoid cells with scattered , pale, tingible body–laden macrophages (“starry sky”
histology)
Burkitt lymphoma (t[8:14] c-myc activation associated with EBV; “starry sky” made up of malignant cells)
51
Lytic (“punched-out”) bone lesions on x-ray
Multiple myeloma
52
Monoclonal antibody spike
-Multiple myeloma (usually IgG or IgA)
- Monoclonal gammopathy of undetermined
significance (MGUS consequence of aging)
-Waldenström (M protein = IgM) macroglobulinemia Primary amyloidosis
53
Stacks of RBCs
Rouleaux formation (high ESR, multiple myeloma)
54
Azurophilic peroxidase ⊕ granular inclusions in granulocytes and myeloblasts
Auer rods (AML, especially the promyelocytic [M3] type)
55
WBCs that look “smudged”
CLL (almost always B cell)
56
“Tennis racket”-shaped cytoplasmic organelles (EM) in Langerhans cells
Birbeck granules (Langerhans cell histiocytosis)
57
“Brown” tumor of bone
Hyperparathyroidism or osteitis fibrosa cystica (deposited hemosiderin from hemorrhage gives brown color)
58
“Soap bubble” in femur or tibia on x-ray
Giant cell tumor of bone (generally benign)
59
Raised periosteum (creating a “Codman triangle”)
Aggressive bone lesion (eg, osteosarcoma, Ewing sarcoma, osteomyelitis)
60
“Onion skin” periosteal reaction
Ewing sarcoma (malignant small blue cell tumor)
61
Anti-IgG antibodies
Rheumatoid arthritis (systemic inflammation, joint pannus, boutonniere and swan neck deformities) RF
62
Rhomboid crystals, ⊕ birefringent
Pseudogout (calcium pyrophosphate dihydrate crystals)
63
Needle-shaped, ⊝ birefringent crystals
Gout (monosodium urate crystals)
64
uric acid levels
Gout, Lesch-Nyhan syndrome, tumor lysis syndrome, loop and thiazide diuretics
65
“Bamboo spine” on x-ray
Ankylosing spondylitis (chronic inflammatory arthritis: HLA-B27)
66
Antinuclear antibodies (ANAs: anti-Smith and anti- dsDNA)
SLE (type III hypersensitivity)
67
Anti-histone antibodies
Drug-induced SLE (eg, hydralazine, isoniazid, phenytoin, procainamide)
68
Anti-topoisomerase antibodies
Diffuse scleroderma
69
Keratin pearls on a skin biopsy
Squamous cell carcinoma
70
Bloody or yellow tap on lumbar puncture
Xanthochromia (due to subarachnoid hemorrhage)
71
Eosinophilic cytoplasmic inclusion in neuron
Lewy body (Parkinson disease and Lewy body dementia)
72
Extracellular amyloid deposition in gray matter of brain
Senile plaques (Alzheimer disease)
73
Depigmentation of neurons in substantia nigra
Parkinson disease (basal ganglia disorder: rigidity, resting tremor, bradykinesia)
74
Protein aggregates in neurons from hyperphosphorylation of tau protein
Neurofibrillary tangles (Alzheimer disease) and Pick bodies (Pick disease)
75
Silver-staining spherical aggregation of tau proteins in neurons
Pick bodies (Pick disease: progressive dementia, changes in personality)
76
Pseudopalisading tumor cells on brain biopsy
Glioblastoma multiforme
77
Circular grouping of dark tumor cells surrounding pale neurofibrils
Homer-Wright rosettes (neuroblastoma, medulloblastoma)
78
“Waxy” casts with very low urine flow
Chronic end-stage renal disease
79
Nodular hyaline deposits in glomeruli
Kimmelstiel-Wilson nodules (diabetic nephropathy)
80
Podocyte fusion or “effacement” on electron microscopy
Minimal change disease (child with nephrotic syndrome)
81
“Spikes” on basement membrane, “dome-like” subepithelial deposits
Membranous nephropathy (nephrotic syndrome)
82
RBC casts in urine
Glomerulonephritis
83
“Tram-track” appearance of capillary loops of glomerular basement membranes on light microscopy
Membranoproliferative glomerulonephritis
84
Anti–glomerular basement membrane antibodies
Goodpasture syndrome (glomerulonephritis and hemoptysis)
85
Cellular crescents in Bowman capsule
Rapidly progressive (crescentic) glomerulonephritis
86
“Wire loop” glomerular capillary appearance on light microscopy
Diffuse proliferative glomerulonephritis (usually seen with lupus)
87
Linear appearance of IgG deposition on glomerular and alveolar basement membranes
Goodpasture syndrome
88
“Lumpy bumpy” appearance of glomeruli on immunofluorescence
Poststreptococcal glomerulonephritis (due to deposition of IgG, IgM, and C3)
89
Necrotizing vasculitis (lungs) and necrotizing glomerulonephritis
Granulomatosis with polyangiitis (Wegener; PR3-ANCA/c-ANCA) and Goodpasture syndrome (anti–basement membrane antibodies)
90
Thyroid-like appearance of kidney
Chronic pyelonephritis (usually due to recurrent infections)
91
WBC casts in urine
Acute pyelonephritis
92
Renal epithelial casts in urine
Intrinsic renal failure (eg, ischemia or toxic injury)
93
hCG elevated
Choriocarcinoma, hydatidiform mole (occurs with and without embryo, and multiple pregnancy)
94
Dysplastic squamous cervical cells with “raisinoid” nuclei and hyperchromasia
Koilocytes (HPV: predisposes to cervical cancer)
95
Disarrayed granulosa cells arranged around collections of eosinophilic fluid
Call-Exner bodies (granulosa cell tumor of the ovary)
96
“Chocolate cyst” of ovary
Endometriosis (frequently involves both ovaries)
97
Mammary gland (“blue domed”) cyst
Fibrocystic change of the breast
98
Glomerulus-like structure surrounding vessel in germ cells
Schiller-Duval bodies (yolk sac tumor)
99
Rectangular, crystal-like, cytoplasmic inclusions in Leydig cells
Reinke crystals (Leydig cell tumor)
100
Thrombi made of white/red layers
Lines of Zahn (arterial thrombus, layers of platelets/RBCs)
101
Hexagonal, double-pointed, needle-like crystals in bronchial secretions
Bronchial asthma (Charcot-Leyden crystals: eosinophilic granules)
102
Desquamated epithelium casts in sputum
Curschmann spirals (bronchial asthma; can result in whorled mucous plugs)
103
“Honeycomb lung” on x-ray or CT
Idiopathic pulmonary fibrosis
104
Colonies of mucoid Pseudomonas in lungs
Cystic fibrosis (autosomal recessive mutation in CFTR gene -> fat-soluble vitamin defic iency and mucous plugs)
105
Iron-containing nodules in alveolar septum
Ferruginous bodies (asbestosis: ^chance of lung cancer)
106
Bronchogenic apical lung tumor on imaging
Pancoast tumor (can compress cervical sympathetic chain and cause Horner syndrome)
