Classic Labs/Findings Flashcards
Anticentromere antibodies
Scleroderma (CREST)
Anti-desmoglein (epithelial) antibodies
Pemphigus vulgaris (blistering)
Anti-glomerular basement membrane antibodies
Goodpasture syndrome (glomerulonephritis and hemoptysis)
Antihistone antibodies
Drug-induced SLE (e.g., hydralazine, isoniazid, phenytoin, procainamide)
Anti-IgG antibodies
Rheumatoid arthritis (systemic inflammation, joint pannus, boutonnière deformity)
Antimitochondrial antibodies (AMAs)
Primary biliary cirrhosis (female, cholestasis, portal hypertension)
Antineutrophil cytoplasmic antibodies (ANCAs)
Microscopic polyangitis and eosinophilia granulomatosis with polyangitis (Churg-Strauss syndrome) (MPO-ANCA/p-ANCA);
Granulomatosis with polyangitis (Wegener; PR3-ANCA/c-ANCA)
Antinuclear antibodies (ANAs:anti-Smith and anti-dsDNA
SLE (type 3 hypersensitivity)
Anti-platelet antibodies
Idiopathic thrombocytopenic purpura
Anti-topoisomerase
Diffuse systemic scleroderma
Anti-transglutaminase/anti-gliadin/anti-endomysial antibodies
Celiac Disease (diarrhea, weight loss)
“Apple core” lesionon barium enema x-ray
Colorectal cancer (usually left-sided)
Atypical lymphocytes
EBV
Azurophilic peroxidase positive granular inclusions in granulocytes and myeloblasts
Auer rods (AML, especially the promyelocytic (M3) type)
Bacitracin response
Sensitive: Streptococcus pyogenes (group A)
Resistant: Streptococcus agalactiae (group B)
“Bamboo spine” on X-ray
Ankylosing spondylitis (chronic inflammatory arthritis: HLA-B27)
Basophilic nuclear remnants in RBCs
Howell-Jolly bodies (due to splenectomy or nonfunctional spleen)
Basophilic stippling of RBCs
Lead poisoning or sideroblastic anemia
Bloody or yellow tap on lumbar puncture
Subarachnoid hemorrhage
“Boot shaped” heart on x-ray
Tetralogy of Fallot (due to RVH)
Branching gram positive rods with sulfur granules
Actinomyces Israeli
Brochogenic apical lung tumor on imaging
Pancoast tumor (can compress cervical sympathetic chain and cause Horner syndrome)
“Brown” tumor of bone
Hyperparathyroidism or osteitis fibrosis cystica (deposited hemosiderin from hemorrhage gives brown color)
Cardiomegaly with apical atrophy
Chagas’ disease (trypanosoma Cruzi)
Cellular crescents in bowman capsule
Rapidly progressive cresenteric glomerulonephritis
‘Chocolate cyst’ of ovary
Endometriosis (frequently involves both ovaries)
Circular Grouping of dark tumor cells surrounding pale neurofibrils
Homer-Wright rosettes (neuroblastoma, medulloblastoma)
Colonies of mucous Pseudomonas in lungs
Cystic fibrosis (AR mutation in CFTR gene—-> fat soluble vitamin deficiency and mucous plugs)
Decrease AFP in amniotic fluid/maternal serum
Down syndrome or other chromosomal abnormalities
Degeneration of dorsal column fibers
Tabes Dorsalis (tertiary syphilis)
Subacute combined degeneration of the spinal cord
(dorsal columns, lateral corticospinal, spinocerebellar tracts affected)
“Delta wave” on EKG, short PR interval, supraventricular tachycardia
Wolf-Parkinson-White syndrome (Bundle of Kent bypasses AV node)
Depigmentation of neurons in substantia nigra
Parkinson Disease (basal ganglia disorder: rigidity, resting tremor, bradykinesia)
Desquamated epithelium casts in sputum
Curschmann spirals (bronchial asthma; can result in whorled mucous plugs)
Disarrayed granulosa cells arranged around collections of eosinophilia fluid
Call-Exner bodies (granulosa cell tumor of the ovary)
Dysplastic squamous cervical cells with “rasinoid” nuclei and hyperchromasia
Koilocytes (HPV: predisposes to cervical cancer)
Electrical alternans (alternating amplitude on EKG)
Pericardial tamponade
Enlarged cells with intranuclear inclusion bodies
“Owl eye” appearance of CMV
Enlarged thyroid cells with ground glass nuclei with central clearing
“Orphan Annie” eyes nuclei (papillary carcinoma of the thyroid)
Eosinophilic cytoplasmic inclusion in liver cell
Mallory body (alcoholic liver disease)
Eosinophilic cytoplasmic inclusion in nerve cell
Lewy body (Parkinson Disease)
Eosinophilic globule in liver
Councilman body (viral hepatitis, yellow fever), represents hepatocyte undergoing apoptosis
Eosinophilic inclusion bodies in cytoplasm of hippocampal and cerebellum neurons
Negri bodies of rabies
Extracellular amyloid deposition in gray matter of brain
Senile plaques (Alzheimer’s disease)
Giant B cells with bilobed nuclei with prominent inclusions (“owls’s eye”)
Reed-Sternberg cells (Hodgkin lymphoma)
Glomerulus-like structure surround vessel in germ cells
Schiller-Duval bodies (yolk sac tumor)
“Hair on end” (“crew cut”) appearance on X-ray
B-thalassemia, sickle cell Disease (marrow expansion)
hCG elevate
Choriocarcionoma, hydatidiform mole (occurs with and without embryo, and multiple pregnancy).
Heart nodules (granulomatous)
Aschoff bodies (Rhuematic fever)
Heterophile antibodies
Infectious mononucleosis (EBV)
Hexagonal, double-pointed, needle like crystals in bronchial secretions
Bronchial asthma (Charcot-Leyden crystals: eosinophilic granules)
High level of D-dimers
DVT, PE,DIC
Hilar lymphadenopathy, peripheral granulomatosis lesion in middle or lower Lung lobes (can calcify)
Ghon complex (primary TB: mycobacterium bacilli)
“Honeycomb lung” on X-ray or CT
Interstitial pulmonary fibrosis
Hypercoagulability (leading to migrating DVTs and vasculitis)
Trousseau syndrome (adenocarcinoma of pancreas or lung)
Hypersegmented neutrophils
Megaloblastic anemia (B12 deficiency: neurological symptoms; folate deficiency:no neurological symptoms)
Hypertension, hypokalemia, metabolic alkalosis
Conn syndrome (primary hyperaldosteronism)
Hypochromic, microcytic anemia
Thalassemia (fetal hemoglobin sometimes present)
A
Iron deficiency anemia
Lead poisoning
Increased AFPmin amniotic fluid or maternal serum
Dating error, anencephaly, spina bifida (NTDs)
Increased Uris acid levels
Gout, Lesch-Nyhan syndrome, tumor lysis syndrome, loop and thiazide diuretics
Intranuclear esosinophilc droplet-like bodies
Cowdry type A bodies (HSV or VZV)
Iron-containing nodules in alveolar septum
Ferruginous bodies (asbestosis: increase chance of mesothelioma)
Keratin pearls on skin biopsy
Squamous cell carcinoma
Large granules in phagocytes, immunodeficiency
Chédiak-Higashi Disease (congenital failure of phagolysosome formation)
“Lead pipe” appearance of colon on abdominal imaging
Ulcerative colitis (loss of haustra)
Linear appearance of IgG deposition on glomerularnand alveolar basement membranes
Goodpasture syndrome
Low serum ceruloplasmin
Wilson disease (hepatolenticular degeneration)
“Lumpy bumpy” appearance of glomeruli on immunofluorescence
Poststreptoccal glomerulonephritis (due to deposition of IgG, IgM and C3)
Lytic “punched out” bone lesion on x-ray
Multiple Myeloma
Mammary gland (“blue domed”) cyst
Fibrocystic change of the breast
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
Mucin-filled cell with peripheral nucleus
“Signet ring” (gastric carcinoma)
Narrowing of bowel lumen on barium X-ray
String sign (Crohn Disease)
Necrotizing vasculitis (lungs) and necrotizing glomerulonephritis
Granulomatosis with polyangitis (Wegener; PR3-ANCA/c-ANCA)
Goodpasture syndrome (anti-basement membrane antibodies)
Needle shaped, negative birefringrnt crystals
Gout (monosodium urate crystals)
Nodular hyaline deposits in glomeruli
Kimmelstiel-Wilson nodules (diabetic nephropathy)
Novobocin response
Sensitive: S.epidermidis
Resistant: S.saprophyticus
“Nutmeg” appearance of liver
Chronic passive congestion of liver due to right heart failure or Budd-Chiari Syndrome
“Onion skin” periosteal reaction
Ewing sarcoma (malignant small blue cell tumor)
Optochin response
Sensitive: S.pnuemoniae
Resistant: Viridans strep (s.mutans, S.sanguis)
Periosteum raised from bone, creating triangular area
Cod an triangle on X-ray , Ewing sarcoma, pyogenic osteomyelitis
Podocyte fusion or effacement on electron microscopy
Minimal change Disease (child with nephrotic syndrome)
Polished, “ivory-like” appearance of bone at cartilage erosion
Eburnation (osteoarthritis resulting in bony Sclerosis)
Protein aggregates in neurons from hyperphosphorylation of tau protein
Neurofibrillary tangles (Alzheimer Disease) and Pick bodies (Pick Disease)
Psammoma bodies
Meninigiomas, papillary thyroid carcinoma, mesothelioma, papillary serous carcinoma of the endometrium and ovary
Pseudopalisading tumor on brain biopsy
Glioblastoma Multiforme
RBc casts in urine
Glomerulonephritis
Rectangular, crystal like, cytoplasmic inclusions in Leydig cells
Reinke crystals (Leydig cell tumor)
Recurrent infections, eczema, thrombocytopenia
Wiskott-Aldrich syndrome
Renal epithelial casts in urine
Intrinsic renal failure (ischemic or toxic)
Rhomboid crystals, positively birefringent
Psuedogout (calcium pyrophosphate dihydrate crystals)
Rib notching
Coarctaion of the aorta
Ring enhancing brain lesions in AIDS
Toxoplasma gondii, CNS lymphoma
Sheets of medium sized lymphoid cells with scattered pale, tangible body-laden macrophages (“starry sky” histology)
Burkitt lymphoma (t[8:14] c-myc activation, associated with EBV; “starry sky” made up of malignant cells)
Silver-staining spherical aggregation of tau proteins in neurons
Pick bodies (pick Disease: progressive dementia, changes in personality)
Soap bubble in femur or tibia on X-ray
Giant cell tumor of bone (generally benign)
“Spikes” on basement membrane “dome-like” subepithelial deposits
Membranous nephropathy (nephrotic syndrome)
Stacks of RBCs
Rouleaux formation (high ESR, multiple myeloma)
“Steeple” sign on CXR
Croup (parainfluenza virus)
Stipples vaginal epithelial cells
“Clue cells” (Gardnerella vaginalis)
Streptococcus bovis bacteremia
Colon cancer
“Tennis racket-shaped cytoplasmic organelles in Langerhans cells
Birbeck granules (langerhans cell histiocytosis)
Thousands of polyps on colonoscopy
Familial adenomatous polyposis (AD mutation of APC gene)
Thrombi made of white/red layers
Lines of Zahn (arterial thrombus, layers of platelets/RBCs)
“Thumb sign” on lateral neck X-ray
Epiglottitis (H.influenza)
Thyroid-like appearance of kidney
Chronic pyelonephritis (usually due to recurrent infections)
“Tram-track” appearance of capillary loops of glomerular basement membranes on light microscopy
Membranoproliferative glomerulonephritis
Triglyceride accumulation in liver cell vacuoles
Fatty liver disease (alcoholic or metabolic syndrome)
Waxy casts with very low urine flow
Chronic end stage renal disease
WBC casts in urine
Acute pyelonephritis
WBCs that look smudged
CLL (almost always B cell)
“Wire loop” glomerular capillary appearance on light microscopy
Diffuse glomerulonephritis (usually seen with lupus)
Yellowish CSF
Xanthochromia (e.g. Due to subarachnoid hemorrhage)