FA - Classic Labs/Findings Flashcards
Antidesmoglein (epitheliall) antibodies
Pemphigus vulgaris (blistering)
Anti-glomerular BM antibodies
Goodpasture (GN + Hemoptysis)
Antihistone antibodies
Drug induced lupus (hydralazine, INH, phenytoin, procainamide)
Anti-IgG antibodies
RA
Antimitochondrial antibodies
PBC
Antineutrophil cytoplasmic antibodies (ANCAs)
c-ANCA (PR3-ANCA) –> Wegener
p-ANCA (MPO-ANCA) –> Microscopic poluangiitis + Churg-Strauss syndrome
Antinuclear antibodies (ANAs: Anti-Smith, anti-dsDNA)
SLE - HRS III.
Antiplatelet antibodies
Idiopathic thrombocytopenic purpura
Anti-topoisomerase antibodies
Diffuse scleroderma
Anti-transglutaminase
Anti-gliadin
Anti-endomysial
Celiac disease
Apple core lesion on abdominal X-ray
Colorectal cancer (usually left-sided)
Azurophilic peroxidase (+) granular inclusions in granulocytes and myeloblasts
Auer rods –> AML M3 –> promyelocytic.
Bacitracin response
Sensitive - Strep pyogenes (group A)
Resistant - Strep agalactiae (group B)
“Bambo spine” on x-ray
Ankylosing spondylitis
Basophilic nuclear remnants in RBCs
Howell-Jolly bodies - due to splenectomy or nonfunctional spleen.
Basophilic stippling of RBCs
- Lead poisoning
2. Sideroblastic anemia
Bloody tap on LP
Subarachnoid hemorrhage
“Boot-shaped” heart on x-ray
- FALLOT
2. RVH
Branching gram(+) rods with sulfur granules
Actinomyces israelii
Bronchogenic apical lung tumor on imaging
Pancoast tumor - can compress sympathetic ganglion and cause Horner syndrome.
“Brown” tumor of bone
Hyperparathyroidism or osteitis fibrosa cystica –> deposited hemosiderin from hemorrhage gives brown color.
Cardiomegaly with apical atrophy
Chagas disease
Cellular crescents in Bowman capsule
Rapidly progressive crescentic GN
“Chocolate cyst” of ovary
Endometriosis - frequently involves both ovaries
Circulating grouping of dark tumor cells surrounding pale neurofibrils
Homer-Wright rosettes:
- Neuroblastoma
- Medulloblastoma
- Retinoblastoma
Colonies of mucoid Pseudomonas in lungs
CF
DOWN AFP in amniotic fluid/maternal serum
Down syndrome or other chromosomal abnormality.
Degeneration of dorsal column nerves
Tabes dorsalis –> 3o syphilis
Subacute combined degeneration –> dorsal columns + lateral corticospinal tracts affected.
Depigmentation of neurons in substantia nigra
Parkinson
Desquamated epithelium casts in sputum
Curschmann spirals
Disarrayed granulosa cells in eosinophilic fluid
Call-Exner bodies –> Granulosa-theca cell tumor of the ovary.
Dysplastic squamous cervical cells with nuclear enlargement + hyperchromasia
Koilocytes
Enlarged cells with intranuclear inclusion bodies
“Owl eye” appearance of CMV
Enlarged thyroid cells with ground-glass nuclei
“Orphan Annie” eyes nuclei –> Papillary carcinoma of the thyroid
Eosinophilic cytoplasmic inclusion in liver cell
Mallory body - Alcohol liver disease.
Eosinophilic cytoplasmic inclusion in nerve cell
Lewy body - Parkinson
Eosinophilic globule in liver
Councilman body –> toxic/viral hepatitis, often yellow fever.
Eosinophilic inclusion bodies in cytoplasm of hippocampal + cerebellar nerve cells
Negri bodies of rabies
Extracellular amyloid deposition in gray matter of brain
Senile plaques –> Alzheimer
Giant B cell with bilobed nuclei with prominent inclusions (“owl’s eye”)
Reed-Sternberg cells (HL)
Glomerulus-like structure surrounding vessel in germ cells
Schiller-Duval bodies –> Yolk sac tumor.
“Hair on end” (crew cut) appearance on x-ray
Beta-thalassemia
SCA –> Marrow expansion
hCG elevated
- Choriocarcinoma
2. Hydatidiform mole –> occurs with and without embryo, and multiple pregnancy.
Heart nodules (granulomatous)
Aschoff bodies (RF).
Heterophile antibodies
IM
Hexagonal, double-pointed, needle-like crystals in bronchial secretions
Bronchial asthma - Charcot-Leyden crystals: eosinophilic granules.
Elevated D-dimers
DVT
PE
DIC
Hilar lymphadenopathy
Peripheral granulomatous lesion in middle or lower lung lobes (can calcify).
Ghon complex –> 1o TB.
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 - EITHER B12 OR FOLATE.
HTN
Hypokalemia
Metabolic alkalosis
Conn syndrome
Hypochromic, microcytic anemia
- Iron def.
- Lead poisoning
- Thalassemia (fetal Hb sometimes present)
Incr. AFP in amniotic fluid/maternal serum
- Dating error
- Anencephaly
- Spina bifida (neural tube defects)
Incr. uric acid levels
- Gout
- Lesch-Nyhan syndrome
- Tumor lysis syndrome
- Loop + Thiazides
Intranuclear eosinophilic droplet-like bodies
Cowdry type A bodies –> HSV or CMV.
Iron-containing nodules in alveolar septum
Ferruginous bodies –> Asbestosis: Incr. risk for mesothelioma.
Keratin pearls on skin biopsy
SCC
Large lysosomal vesicles in phagocytes
Immunodeficiency
Chediak-Higashi
“Lead pipe” appearance of colon on barium enema x-ray
UC (loss of haustra)
Linear appearance of IgG deposition on glomerular BM
Goodpasture
Low serum ceruloplasmin
Wilson disease - Hepatolenticular degeneration.
“Lumpy bumpy” appearance off glomeruli on immunofluorescence
Poststreptococcal GN –> Immune complex deposition of IgG and C3b.
Lytic (“hole punched”) bone lesions on x-ray
Multiple myeloma
Mammary gland (“blue domed”) cyst
Fibrocystic change of the breast
Monoclonal antibody spike
- Multiple myeloma (usually IgG, or IgA)
- MGUS –> consequence of aging.
- Waldenstrom (M protein = IgM)
- Primary amyloidosis
Mucin-filled cell with peripheral nucleus
“Signet ring”
Narrowing of bowel lumen on barium x-ray
String sign - Crohn disease
Necrotizing vasculitis (lungs) + Necrotizing GN
- Granulomatosis with polyangiitis - Wegener
2. Goodpasture
Needle-shaped, negatively birefringent crystals
Gout - monosodium urate crystals.
Nodular hyaline deposits in glomeruli
Kimmelstiel-Wilson nodules - Diabetic nephropathy
Novobiocin response
Sensitive –> S.epi
Resistant –> S.sapro
Nutmeg liver
CHRONIC passive congestion of live due to RHF.
“Onion skin” periosteal reaction
Ewing sarcoma - malignant ROUND cell tumor.
Optochin response
Sensitive –> S.pneumo
Resistant –> Viridans strep
Periosteum raised from bone –> Creating triangular area
Codman triangle on x-ray –>
- Osteosarcoma
- Ewing
- Pyogenic osteomyelitis
Podocyte fusion or “effacement” on electron microscopy
Minimal change disease - child with nephrotic syndrome.
Polished, “ivory-like” appearancce of bone at cartilage erosion
Eburnation –> Osteoarthritis resulting in bony sclerosis.
Protein aggregates in neurons from hyperphosphorylation of tau protein
- Neurofibrillary tangles - Alzheimer
2. Pick bodies - Pick
Psammoma bodies
- Meningiomas
- Papillary thyroid carcinoma
- Mesothelioma
- Papillary serous carcinoma of the endometrium and ovary
Pseudopalisading tumor cells on brain biopsy
Glioblastoma multiforme
RBC cast in urine
Acute GN
Rectangular, crystal-like, cytoplasmic inclusions in Leydig cells
Reinke crystals –> Leydig cell tumor.
Renal epithelial casts in urine
Acute toxic/viral renal injury
Rhomboid crystals, positively birefringent
Pseudogout –> Ca pyrophosphate dihydrate crystals
Rib notching
COTA
Ring-enhancing brain lesions in AIDS
- T.gondii
2. CNS lymphoma
Sheets of medium-sized lymphoid cells with scattered pale, tingible body-laden macrophages –> starry sky histology.
Burkitt
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 the bone - usually benign.
“Spikes” on BM, “dome-like” subepithelial deposits
Membranous GN –> May progress to nephrotic syndrome.
Stacks of RBCs
Rouleaux formation –> High ESR, MM.
Stippled vaginal epithelial cells
“Clue cells” - G.vaginalis
“Tennis racket”-shaped cytoplasmic organelles (EM) in Langerhans cells
Birbeck granules:
- Langerhans cell histiocytosis
- Histiocytosis X: eosinophilic granuloma
Thrombi made of white/red layers
Lines of Zahn –> Arterial thrombus, layers of platelets/RBCs
“Thumb sign” on lateral x-ray
Epiglottitis - H.influenza
Thyroid-like appearance of kidney
Chronic bacterial pyelonephritis
“Tram track” appearance of capillary loops of glomerular BM on light microscopy
Membranoproliferative GN
TGs 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
“Wire loop” glomerular capillary appearance on light microscopy
Lupus nephropathy
Yellowish CSF
Xanthocromia –> Due to subarachnoid hemorrhage.
Antidentromere antibodies
Scleroderma (CREST)