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336 Cards in this Set

  • Front
  • Back
Precursor to squamous cell carcinoma
Actinic (solar) keratosis
Cushing's ulcer (increased ICP stimulates vagal gastric secretion)
Acute gastric ulcer associated with CNS injury
Curling's ulcer (greatly reduced plasma volume results in sloughing of gastric mucosa)
Acute gastric ulcer associated with severe burns
Skip lesions (alternating areas of transmural inflammation and normal colon).
Crohn's disease
Aneurysm, dissecting
Hypertension
Aortic aneurysm, abdominal and descending aorta
Atherosclerosis
Aortic aneurysm, ascending
Tertiary syphilis, Marfan's syndrome
Atrophy of the mammillary bodies
Wernicke's encephalopathy (thiamine deficiency causing ataxia, ophthalmoplegia, and confusion).
Autosplenectomy (fibrosis and shrinkage)
Sickle cell anaemia (HbS)
Bacteria associated with stomach cancer
H. pylori
Bacterial meningitis (adults and elderly)
Neisseria meningitidis
Bacterial meningitis (newborns and kids)
Group B streptococcus (newborns); S.pneumoniae/Neisseria meningitidis (kids).
Benign melanocytic nevus
Spitz nevus (most common in first 2 decades)
Bleeding disorder with GpIb deficiency
Bernard-Soulier disease (defect in platelet adhesion to von Willebrand's factor).
Brain tumour (adults)
Supratentorial: mets > astrocytoma (including glioblastoma multiforme) > meningioma > schwannoma
Brain tumour (kids)
Infratentorial: medulloblastoma (cerebellum) or
Supratentorial: craniopharyngioma (cerebrum)
Breast cancer
Infiltrating ductal carcinoma (in US, 1/9 women will develop breast cancer)
Breast mass
1. Fibrocystic change; 2. Carcinoma (postmenopausal women)
Breast tumour (benign)
Fibroadenoma
Cardiac primary tumour (kids)
Rhabdomyoma
Cardiac manifestations of lupus.
Libman-Sacks endocarditis (nonbacterial, affecting mitral)
Cardiac tumour (adults)
1. Metastasis; 2. Primary myxoma (4:1 left to right atrium; 'ball and valve')
Cerebellar tonsillar herniation
Chiari malformation (often presents with progressive hydrocephalus or syringomyelia)
Chronic arrhythmia
Atrial fibrillation (associated with high risk of emboli)
Chronic atrophic gastritis (autoimmune)
Predisposition to gastric carcinoma (can also cause pernicious anemia)
Clear cell adenocarcinoma of the vagina
DES exposure in utero
Congenital adrenal hyperplasia, hypotension
21-hydroxylase deficiency
Congenital cardiac anomaly
VSD
Congenital conjugated hyperbilirubinemia (black liver)
Dubin-Johnson syndrome (inability of hepatocytes to secrete conjugated bilirubin into bile)
Constrictive pericarditis in developing world.
Tuberculosis
Coronary artery involved in thrombosis
LAD > RCA > LCA
Cretinism
Iodine deficit/hypothyroidism
Cushing's syndrome
1. Corticosteroid therapy; 2. Excess ACTH secretion by pituitary
Cyanosis (early; less common)
Tetralogy of Fallot, transposition of great vessels, truncus arteriosus
Cyanosis (late; more common)
VSD, ASD, PDA
Death in CML
Blast crisis
Death in SLE
Lupus nephropathy
Dementia
1. Alzheimer's disease; 2. Multiple infarcts
Demyelinating disease in young women
Multiple sclerosis
DIC
Gram negative sepsis; obstetric complications, cancer, burn trauma
Dietary deficit
Iron
Diverticulum in pharynx
Zenker's diverticulum (diagnosed by barium swallow)
Ejection click
Aortic/pulmonic stenosis
Esophageal cancer
Squamous cell carcinoma (worldwide); adenocarcinoma (US)
Food poisoning (exotoxin mediated)
S. aureus, B. cereus
Glomerulonephritis (adults)
Berger's disease (IgA nephropathy)
Gynecological malignancy
Endometrial carcinoma (most common)
Heart murmur, congenital
Mitral valve prolapse
Heart valve in bacterial endocarditis
Mitral (rheumatic fever), tricuspid (IV drug abuse), aortic (2nd affected in rheumatic fever)
Helminth infection (US)
1. Enterobius vermicularis; 2. Ascaris lumbricoides
Rupture of middle meningeal artery (crescent shaped)
Epidural hematoma
Rupture of bridging veins (trauma; lentiform shaped)
Subdural hematoma
Hemochromatosis
Multiple blood transfusions or hereditary HFE mutation (can result in CHF, 'bronze diabetes', and increased risk of HCC)
Hepatocellular carcinoma
Cirrhotic liver (often associated with HBV and HCV)
Hereditary bleeding disorder
von Willebrand's diseas
Hereditary harmless jaundice
Gilbert's syndrome (benign congenital unconjugated hyperbilirubinemia)
HLA-B27
Ankylosing spondylitis, Reiter's syndrome, ulcerative colitis, psoriasis
HLA-DR3 or -DR4
Diabetes mellitus type 1, rheumatoid arthritis, SLE
Holosystolic murmur
VSD, tricuspid regurgitation, mitral regurgitation
Hypercoagulability, endothelial damage, blood stasis
Virchow's triad (results in venous thrombosis)
Secondary hypertension
renal disease
Hypoparathyroidism
Thyroidectomy
Hypopituitarism
Pituitary adenoma (usually benign tumour)
Infection secondary to blood transfusion
HCV
Kidney stones
1. Calcium; 2. Struvite (ammonium - formed by urease-positive organisms such as proteus vulgaris or staphylococcus); 3. Uric acid (radiolucent)
Late cyanotic shunt (uncorrected L --> R becomes R --> L)
Eisenmenger's syndrome (caused by ASD, VSD, PDA; results in pulmonary hypertension/polycythemia)
Liver disease
Alcoholic cirrhosis
Lysosomal storage disease
Gaucher's disease
Male cancer
Prostatic carcinoma
Malignancy associated with noninfectious fever
Hodgkin's lymphoma
Malignant skin tumour
Basal cell carcinoma (rarely metastasizes)
Mental retardation
1. Down syndrome; 2. Fragile X syndrome
Metastases to bone
Lung, Breast, Prostate, Thyroid, Testes, Kidney
Metastases to brain
Lung, breast, skin (melanoma), kidney (renal cell carcinoma), GI
Metastases to liver
Colon, gastric, pancreatic, breast, and lung carcinoma
Mitral valve stenosis
Rheumatic heart disease
Mixed UMN and LMN motor neuron disease
ALS
Myocarditis
Coxsackie B
Neoplasms (kids)
1. ALL; 2. Cerebellar medulloblastoma
Nephrotic syndrome (adults)
Membranous GN
Nephrotic syndrome (kids)
Minimal change disease (associated with infections/vaccinations; treat with corticosteroids)
Nosocomial pneumonia
Klebsiella, E. coli, Pseudomonas aeruginosa
Obstruction of male urinary tract
BPH
Opening snap
Mitral stenosis
Opportunistic infection in AIDS
Pneumocystis jiroveci (formerly carinii) pneumonia
Osteomyelitis
S. aureus
Osteomyelitis in sickle cell disease patients
Salmonella
Ovarian metastasis from gastric carcinoma or breast cancer.
Krukenberg tumour (mucin-secreting signet-ring cells)
Ovarian tumour (benign)
Serous cystadenoma
Ovarian tumour (malignant)
Serous cystadenocarcinoma
Pancreatitis (acute)
Gallstones, alcohol
Pancreatitis (chronic)
Alcohol (adults), cystic fibrosis (kids)
Patient with ALL/CLL/AML/CML
ALL: child;
CLL: adult >60
AML: adult >60
CML: adult 35-50
Pelvic inflammatory disease
Neisseria gonorrhoea (monoarticular arthritis)
Philaedelphia chromosome
t(9;22) bcr-abl.
CML (may sometimes be associated with ALL/AML)
Pituitary tumour
1. Prolactinoma; 2. Somatotropic 'acidophilic' adenoma
Primary amenorrhea
Turner syndrome (XO)
Primary bone tumour (adults)
Multiple myeloma
Primary hyperaldosteronism
Adenoma of adrenal cortex
Primary hyperparathyroidism
1. Adenomas; 2. Hyperplasia; 3. Carcinoma
Primary liver cancer
Hepatocellular carcinoma (chronic hepatitis, cirrhosis, hemochromatosis, alpha-1 antitrypsin)
Pulmonary hypertension
COPD
Recurrent inflammation/thrombosis of small/medium vessels in extremities
Buerger's disease (strongly associated with tobacco)
Renal tumour
Renal cell carcinoma: associated with von Hippel-Lindau and adult polycystic kidney disease; Paraneoplastic syndromes (erythropoietin, renin, PTH, ACTH)
Right heart failure due to a pulmonary cause
Cor pulmonale
S3 (protodiastolic gallop)
Increased ventricular filling (L-->R shunt, mitral regurgitation, LV failure)
S4 (presystolic gallop)
Stiff/hypertrophic ventricle (aortic stenosis, restrictive cardiomyopathy)
Secondary hyperparathyroidism
Hypocalcemia of chronic kidney disease
Sexually transmitted disease
Chlamydia (usually coinfected with gonorrhea)
SIADH
Small cell carcinoma of the lung
Site of diverticula
Sigmoid colon
Sites of atherosclerosis
Abdominal aorta > coronary > popliteal > carotid
Stomach cancer
Adenocarcinoma
Stomach ulcerations and high gastrin levels
Zollinger-Ellison syndrome (gastrinoma of duodenum or pancreas)
t(14;18)
Follicular lymphomas (bcl-2 activation)
t(8; 14)
Burkitt's lymphoma (c-myc activation)
t(9;22)
Philadelphia chromosome, CML (bcr-abl hybrid)
Temporal arteritis
Risk of ipsilateral blindness due to thrombosis of ophthalmic artery; polymyalgia rheumatica
Testicular tumour
Seminoma
Thyroid cancer
Papillary carcinoma
Tumour in women
Leiomyoma (estrogen dependent)
Tumour of infancy
Hemangioma (usually regresses spontaneously by childhood)
Tumour of the adrenal medulla (adults)
Pheochromocytoma (usually benign)
Tumour of the adrenal medulla (kids)
Neuroblastoma (malignant)
Type of Hodgkin's
Nodular sclerosis (vs. mixed cellularity, lymphocytic predominance, lymphocytic depletion)
Type of non-Hodgkin's
Diffuse large cell
UTI
E. coli, Staph saprophyticus (young women)
Viral encephalitis affecting temporal lobe
HSV
Vitamin deficiency (US)
Folic acid (pregnant women are at high risk; body stores only 3- to 4-month supply; prevents neural tube defects
Abdominal pain, ascites, hepatomegaly
Budd-Chiari syndrome (posthepatic venous thrombosis)
Achilles tendon xanthoma
Familial hypercholesterolemia (high LDL)
Adrenal hemorrhage, hypotension, DIC
Waterhouse-Friderichsen syndrome (meningoccemia)
Arachnodactyly, lens dislocation, aortic dissection, hyperflexible joints
Marfan's syndrome (fibrillin defect)
Athlete with polycythemia
EPO injection
Back pain, fever, night sweats, weight loss
Pott's disease (vertebral tuberculosis)
Bilateral hilar adenopathy, uveitis
Sarcoidosis (noncaseating granulomas)
Blue sclera
Osteogenesis imperfecta (type I collagen)
Bluish line on gingiva
Burton's line (lead poisoning)
Bone pain, bone enlargement, arthritis
Paget's disease of bone (increased osteoblastic and osteoclastic function
Bounding pulses, diastolic heart murmur, head bobbing
Aortic regurgitation
Cafe-au-lait spots, Lisch nodules (iris hamartoma)
Neurofibromatosis type 1 (+pheochromocytoma, optic gliomas)
Neurofibromatosis type II (+bilateral acoustic neuromas)
Cafe-au-lait spots, polyostotic fibrous dysplasia, precocious puberty
McCune Albright syndrome (mosaic G-protein signaling mutation)
Calf pseudohypertrophy
Muscular dystrophy (most commonly Duchenne)
Cherry red spot on macula
Tay-Sachs (ganglioside accumulation) or Niemann-Pick (sphingomyelin accumulation), central retinal artery occlusion
Chest pain, pericardial effusion/friction rub, persistent fever following MI
Dressler's syndrome (autoimmune-mediated post-MI fibrinous pericarditis, 1-12 weeks after acute episode)
Child uses arms to stand up from squat
Gower's sign (Duchenne muscular dystrophy: X-linked recessive deleted dystrophin gene)
Child with fever develops red rash on face that spreads to body
"slapped cheeks" (erythema infectiosum/fifth disease: parvovirus B19)
Chorea, dementia, caudate degeneration
Huntington's disease (autosomal-dominant CAG repeats)
Chronic exercise intolerance with myalgia, fatigue, painful cramps
McArdle's disease (muscle phosphorylase deficiency)
Cold intolerance
Hypothyroidism
Conjugate lateral gaze palsy, horizontal diplopia
Internuclear ophthalmoplegia (damage to MLF; bilateral [MS], unilateral [stroke])
Continuous 'machinery' heart murmur
PDA (close with indomethacin, open with misoprostol)
Cutaneous/dermal edema due to connective tissue deposition
Myxedema (hypothyroidism, Graves' disease)
Dark purple skin/mouth nodules
Kaposi sarcoma (usually AIDS patients [gay men]: associated with HHV-8)
Deep, laboured breathing/hyperventilation
Kussmaul breathing (DKA)
Dermatitis, dementia, diarrhea
Pellagra (niacin [vitamin B3] deficiency)
Dilated cardiomyopathy, edema, polyneuropathy
Wet beriberi (thiamine [vitamin B1] deficiency)
Dog or cat bite resulting in infection
Pasteurella multocida (cellulitis at inoculation site)
Dry eyes, dry mouth, arthritis
Sjogren's syndrome (autoimmune destruction of exocrine glands)
Dysphagia (esophageal webs), glossitis, iron deficiency anemia
Plummer-Vinson syndrome (may progress to esophageal SCC)
Elastic skin, hypermobility of joints
Ehlers-Danlos syndrome (collagen defect - usually type III)
Enlarged, hard left supraclavicular node
Virchow's node (abdominal metastasis)
Erythroderma (exfoliative dermatitis - erythema and scaling), lymphadenopathy, hepatosplenomegaly, atypical T cells
Sezary syndrome (cutaneous T-cell lymphonma) or mycosis fungoides
Facial muscle spasm upon tapping
Chvostek's sign (hypocalcemia)
Fat, female, forty, and fertile
Cholelithiasis
Fever, chills, headache, myalgia following antibiotic treatment for syphilis
Jarisch-Herxheimer reaction (rapid lysis of spirochetes results in toxin release)
Fever, cough, conjunctivitis, coryza, diffuse rash
Measles (Morbillivirus)
Fever, night sweats, weight loss
B symptoms (lymphoma, TB)
Fibrous plaques in soft tissue of penis
Peyronie's disease (connective tissue disorder)
Gout, mental retardation, self-mutilating behaviour in a boy
Lesch-Nyhan syndrome (HGPRT deficiency, X-linked recessive)
Green-yellow rings around peripheral cornea
Kayser-Fleischer rings (copper accumulation from Wilson's disease)
Hamartomatous GI polyps, hyperpigmentation of mouth/feet/hands
Peutz-Jeghers syndrome (genetic benign polyposis can cause bowel obstruction; increased cancer risk)
Hepatosplenomegaly, osteoporosis, neurologic symptomsq
Gaucher's disease (glucocerebrosidase deficiency)
Hereditary nephritis, sensorineural hearing loss, cataracts
Alport's syndrome (type IV collagen mutation)
Hypercoagualability (leading to migrating DVTs and vasculitis
Trousseau's sign of malignancy (adenocarcinoma of pancreas or lung)
Hyperphagia, hypersexuality, hyperorality, hyperdocility
Kluver-Bucy syndrome (bilateral amygdala lesion)
Hypertension, hypokalemia, metabolic acidosis
Conn's syndrome (primary hyperaldosteronism)
Hypoxemia, polycythemia, hypercapnia
'Blue bloater' (chronic bronchitis: hyperplasia of mucous cells)
Indurated, ulcerated genital lesion
Nonpainful: chancre (primary syphilis, Treponema pallidum)
Painful with exudate: chancroid (Haemophilus ducreyi)
Infant with failure to thrive, hepatosplenomegaly, neurodegeneration
Niemann-Pick disease (genetic sphingomyelinase deficiency)
Infant with failure to thrive, hepatomegaly, hypoglycemia
Cori's disease (debranching enzyme deficiency)
Infant with microcephaly, rocker-bottom feet, clenched hands, and structural heart defect
Edward's syndrome (trisomy 18)
Jaundice, RUQ pain, fever
Charcot's triad 2 (ascending cholangitis)
Keratin pearls on a skin biopsy
SCC
Large rash with bull's eye appearance
Large rash with bull's eye appearance
Erythema chronicum migrans from Ixodes tick bite (Lyme disease)
Lucid interval after traumatic brain injury
Epidural hematoma (middle meningeal artery rupture)
Male child, recurrent infections, no mature B cells
Bruton's disease (X-linked agammaglobulinemia)
Mucosal bleeding and prolonged bleeding time due to lack of GpIIb/IIIa on platelets
Glanzmann's thrombasthenia (defect in platelet aggregation due to lack of GpIIb/IIIa)
Multiple colon polyps, osteomas/soft tissue tumours, impacted/supernumerary teeth
Gardner's syndrome (subtype of FAP)
Necrotizing vasculitis (lungs) and necrotizing glomerulonephritis
Wegener's (c-ANCA positive) and Goodpasture's syndromes (anti-basement membrane antibodies)
Neonate with arm paralysis following difficult birth
Erb-Duchenne palsy (superior trunk [C5-C6] brachial plexus injury: 'waiter's tip')
No lactation postpartum, absent menstruation, cold intolerance
Sheehan's syndrome (pituitary infarction)
Nystagmus, intention tremor, scanning speech
Charcot's triad 1 (for MS)
Also characteristic for bilateral internuclear ophthalmoplegia
Oscillating slow/fast breathing
Cheyne-Stokes respiration (central apnea in CHF or increased intracranial pressure)
Painful blue fingers/toes, hemolytic anemia
Cold agglutin disease (autoimmune hemolytic anemia caused by Mycoplasma pneumoniae, infectious mononucleosis)
Painful, pale, cold fingers/toes
Raynaud's syndrome (vasospasm in extremities)
Painful, raised red lesions on palms and soles
Osler's node (infective endocarditis)
Painless erythematous lesions on palms and soles
Janeway lesions (infective endocarditis)
Painless jaundice
Cancer of pancreatic head obstructing bile duct
Palpable purpura, joint pain, abdominal pain (child)
Henoch-Schonlein purpura (IgA vasculitis affecting skin and kidneys)
Pink complexion, dyspnea, hyperventilation
'Pink puffer' (emphysema: centroacinar [smoking], panacinar [alpha 1 antitrypsin deficiency])
Red current stool
Interssusception
Rusty coloured sputum
Strep pneumonia
Polyuria, acidosis, growth failure, electrolyte imbalances
Fanconi's syndrome (PCT defect)
Positive anterior 'drawer sign'
Anterior cruciate ligament injury
Ptosis, miosis, anhidrosis
Horner's syndrome (sympathetic chain lesion)
Pupil accommodates but doesn't react
Argyll Robertson pupil (neurosyphilis)
Rapidly progressive leg weakness that ascends (following GI/upper respiratory infection
Guillain-Barre syndrome (autoimmune acute inflammatory demyelinating polyneuropathy)
Rash on palms and soles
Secondary syphilis, Rocky Mountain spotted fever, coxsackie A virus (hand-foot disease)
Recurrent colds, unusual eczema, high serum IgE
Job's syndrome (hyper-IgE syndrome: neutrophil chemotaxis abnormal)
Red 'current jelly' sputum in alcoholic or diabetic patients
Klebsiella pneumoniae
Red, itchy, swollen rash of nipple/areola
Paget's disease of the breast (represents underlying neoplasm)
Red urine in the morning, fragile RBCs
Paroxysmal nocturnal hemoglobulinuria
Renal cell carcinoma, hemangioblastomas, angiomatosis, pheochromocytoma
von Hippel-Lindau disease (dominant tumour suppressor gene mutation)
Resting tremor, rigidity, akinesia, postural instability
Parkinson's disease (nigrostriatal DA depletion)
Restrictive cardiomyopathy (juvenile form: cardiomegaly), exercise intolerance
Pompe's disease (lysosomal glucosidase deficiency)
Retinal hemorrhages with pale centers
Roth's spots (bacterial endocarditis)
Severe jaundice in neonate
Crigler-Najjar syndrome (congenital unconjugated hyperbilirubinemia)
Severe RLQ pain with rebound tenderness
McBurney's sign (appendicitis)
Short stature, increased incidence of tumours/leukemia, aplastic anemia
Fanconi's anemia (genetically inherited; often progresses to AML)
Single palm crease
Simian crease (Down syndrome)
Situs invertus, chronic sinusitis, bronchiectasis, infertility
Kartagener's syndrome (dynein defect affecting cilia)
Skin hyperpigmentation
Addison's disease (primary adrenocortical insufficiency of autoimmune or infectious etiology)
Slow, progressive muscle weakness in boys
Becker's muscular dystrophy (X-linked, defective dystrophin; less severe than Duchenne's)
Small, irregular red spots on buccal/lingual mucosa with blue-white centers
Koplik spots (measles)
Smooth, flat, moist white lesions on genitals
Condylomata lata (secondary syphilis)
Splinter hemorrhages in fingernails
Bacterial endocarditis
'Strawberry tongue'
Scarlet fever, Kawasaki disease, toxic shock syndrome
Streak ovaries, congenital heart disease (coarctation of the aorta), horseshoe kidney
Turner syndrome (XO, short stature, webbed neck, lymphedema)
Sudden swollen/painful big toe joint, tophi
Gout/podagra (hyperuricemia)
Swollen gums, mucous bleeding, poor wound healing, spots on skin
Scurvy (vitamin C deficiency: can't hydroxylate proline/lysine for collagen synthesis)
Swollen, hard, painful finger joints
Osteoarthritis (osteophytes on PIP [Bouchard's nodes], DIP [Heberden's nodes])
Systolic ejection murmur (crescendo-decrescendo)
Aortic valve stenosis
Thyroid and parathyroid tumours, pheochromocytoma
Sipple's syndrome (MEN 2A)
Toe extension/fanning upon plantar scrape
UMN lesion (Babinski's sign)
Unilateral facial drooping involving forehead
Bell's palsy (LMN CN VII palsy).
Bilateral - Lyme disease, Guillain-Barre syndrome
Urethritis, conjunctivitis, arthritis in a male
Reiter's syndrome (reactive arthritis associated with HLA-B27)
Vascular birthmark (port-wine stain)
Hemangioma (benign, but associated with Sturge-Weber syndrome)
Vasculitis from exposure to endotoxin causing glomerular thrombosis
Shwartzman reaction (following second exposure to endotoxin)
Vomiting blood following esophagogastric lacerations
Mallory-Weiss syndrome (alcoholic and bulimic patients)
'Waxy' casts with very low urine flow
Chronic end-stage renal disease
WBC casts in urine
Acute pyelonephritis
Weight loss, diarrhea, arthritis, fever, adenopathy
Whipple's disease (Tropheryma whippelii)
'Worst headache of my life'
Subarachnoid hemorrhage
t (11; 22)
Ewing sarcoma
Anticentromere antibodies
Scleroderma (CREST)
Antidesmoglein (epithelial) antibodies
Pemphigus vulgaris (blistering)
Anti-glomerular basement membrane antibodies
Goodpasture's syndrome (glomerulonephritis and hemoptysis)
Antihistone antibodies
Drug-induced SLE (sulpha drugs, hydralazine, isoniazid, phenytoin, procainamide)
Anti-IgG antibodies
Rheumatoid arthritis (rheumatoid factor)
Antimitochondrial antibodies (AMAs)
Primary biliary cirrhosis (female, cholestasis, portal hypertension)
Antineutrophil cytoplasmic antibodies (ANCAs)
Vasculitis (c-ANCA: Wegener's; p-ANCA: microscopic polyangitis, Churg-Strauss syndrome, Pauci immune crescentic glomerulonephritis)
Antinuclear antibodies (ANAs: anti-Smith and anti-dsDNA)
SLE (type III hypersensitivity)
Antiplatelet antibodies
Idiopathic thrombocytopenic purpura (ITP) (bleeding diathesis)
Anti-topoisomerase antibodies
Diffuse systemic scleroderma
Anti-transglutaminase/antigliadin/anti-endomysial antibodies
Celiac disease (diarrhea, distention, weight loss)
Azurophilic granular needles in leukemic blasts
Azurophilic granular needles in leukemic blasts
Auer rods (AML - especially the promyelocytic type)
"Bamboo spin" on xray
Ankylosing spondylitis (chronic inflammatory arthritis; HLA-B27)
Basophilic nuclear remnants in RBCs
Basophilic nuclear remnants in RBCs
Howell-Jolly bodies (due to splenectomy or nonfunctional spleen)
Basophilic stippling of RBCs
Basophilic stippling of RBCs
Lead poisoning or sideroblastic anaemia
Bloody tap on LP
Subarachnoid hemorrhage
"Boot-shaped" heart on xray
Tetralogy of Fallot, RVH
Branching gram-positive rods with sulfur granules
Actinomyces israelii
Bronchogenic apical lung tumour
Pancoast's tumour (can compress sympathetic ganglion and cause Horner's syndrome)
"Brown" tumour of bone
Hemorrhage (hemosiderin) causes brown colour of osteolytic cysts due to:
1. hyperparathyroidism
2. osteitis fibrosa cystica
Cardiomegaly with apical atrophy
Chagas' disease (Trypanosoma cruzi)
Cellular crescents in Bowman's capsule
Rapidly progressive crescentic glomerulonephritis
"Chocolate cyst" on ovary
Endometriosis (frequently involves both ovaries)
Circular grouping of dark tumour cells surrounding pale neurofibrils
Circular grouping of dark tumour cells surrounding pale neurofibrils
Homer Wright rosettes (neuroblastoma, medulloblastoma, retinoblastoma)
Colonies of mucoid Pseudomonas in lungs
Cystic fibrosis (CFTR mutation in Caucasians resulting in fat-soluble vitamin deficiency and mucous plugs)
Degeneration of dorsal column nerves
Tabes dorsalis (tertiary syphilis)
Depigmentation of neurons in substantia nigra
Parkinson's disease
Desquamated epithelium casts in sputum
Curschmann's spirals (bronchial asthma; can result in whorled mucous plugs)
Disarrayed granulosa cells in eosinophilic fluid
Disarrayed granulosa cells in eosinophilic fluid
Call-Exner bodies (granulosa-theca cell tumour of ovary)
Dysplastic squamous cervical cells with nuclear enlargement and hyperchromasia
Dysplastic squamous cervical cells with nuclear enlargement and hyperchromasia
Koilocytes (HPV: predisposes to cervical cancer)
Enlarged cells with intranuclear inclusion bodies
Enlarged cells with intranuclear inclusion bodies
"Owl's-eye" appearance of CMV`
Enlarged thyroid cells with ground-glass nuclei
Enlarged thyroid cells with ground-glass nuclei
"Orphan Annie" eye nuclei (papillary carcinoma of thyroid
Eosinophilic cytoplasmic inclusion in liver cells
Eosinophilic cytoplasmic inclusion in liver cells
Mallory bodies (alcoholic liver disease)
Eosinophilic cytoplasmic inclusion in nerve cell
Eosinophilic cytoplasmic inclusion in nerve cell
Lewy body (Parkinson's disease)
Eosinophilic globule in liver
Eosinophilic globule in liver
Councilman body (viral hepatitis, often yellow fever)
Eosinophilic inclusion bodies in cytoplasm of hippocampal nerve cells
Rabies virus (Lyssavirus)
Extracellular amyloid deposition in gray matter of brain
Senile plaques (Alzheimer's disease)
Giant B cells with bilobed nuclei with prominent inclusions ("owl's eye")
Reed-Sterberg cells (Hodgkin's lymphoma)
Glomerulus-like structure surrounding vessel in germ cells
Schiller-Duval bodies (yolk sac tumour)
"Hair-on-end" (crew cut) appearance on xray
B-thalassemia, sickle cell anemia (extramedullary hematopoiesis)
hCG elevated
Choriocarcinoma, hydatiform mole (occurs with and without embryo)
Heart nodules (inflammatory)
Heart nodules (inflammatory)
Aschoff bodies (rheumatic 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, Budd-Chiari syndrome
Hilar lymphadenopathy, peripheral granulomatous lesion in middle or lower lung lobes (can calcify)
Ghon focus (primary TB: Mycobacterium bacilli)
"Honeycomb lung" on xray
Interstitial fibrosis
Hypersegmented neutrophils
Megaloblastic anemia (B12, folate deficiency)
Hypochromic, microcytic anemia
Iron deficiency anemia, lead poisoning, thalassemia (HbF sometimes present)
Increased alpha-fetoprotein in amniotic fluid/maternal serum
Anencephaly, spina bifida (neural tube defects)
Increased uric acid levels
Gout, Lesch-Nyhan syndrome, tumour lysis syndrome, loop and thiazide diuretics
Intranuclear eosinophilic droplet-like bodies
Cowdry type A bodies (HSV or CMV)
Iron containing nodules in alveolar septum
Ferruginous bodies (asbestosis)
Large lysosomal vesicles in phagocytes, immunodeficiency
Chediak-Higashi disease (congenital failure of phagolysosome formation)
Low serum ceruloplasmin
Wilson's disease (hepatolenticular degeneration)
"Lumpy-bumpy" appearance of glomeruli on immunofluorescence
Poststreptococcal glomerulonephritis
Lytic ("hole punched") bone lesions on xray
Multiple myeloma
Mammary gland ("blue domed") cyst
Fibrocystic change of the breast
Monoclonal antibody spike
1. Multiple myeloma (called M protein; usually IgG or IgA)
2. Monoclonal gammopathy of undetermined significance (MGUS; normal consequence of aging)
3. Waldenstrom's (M protein = IgM) macroglobulinemia
4. Primary amyloidosis
Monoclonal globulin protein in blood/urine
Bence Jones proteins (multiple myeloma [kappa or lambda Ig light chains in urine]), Waldenstrom's macroglobulinemia (IgM)
Mucin-filled cell with peripheral nucleus
Signet ring (gastric carcinoma)
Narrowing of bowel lumen on barium radiograph
"String sign" (Crohn's disease)
Needle-shaped, negatively bifringent crystals
Gout (hyperuricemia)
Nodular hyaline deposits in glomeruli
Kimmelstiel-Wilson nodules (diabetic nephropathy)
"Nutmeg" appearance of liver
Chronic passive congestion of liver due to right heart failure
"Onion-skin" periosteal reaction
Ewing sarcoma (malignant round-cell tumour)
Periosteum raised from bone, creating triangular area
Codman's triangle on xray (osteosarcoma, pyogenic osteomyelitis)
Podocyte fusion on EM
Minimal change disease (child with nephrotic syndrome)
Polished "ivory-like" appearance of bone at cartilage erosion
Eburnation (OA resulting in bony sclerosis)
Protein aggregates in neurons from hyperphosphorylation of protein tau
Neurofibrillary tangles (Alzheimer's disease and CJD)
Pseuodopalisading tumour cells on brain biopsy
Glioblastoma multiforme
RBC casts in urine
Acute glomerulonephritis
Rectangular, crystal-like cytoplasmic inclusions in Leydig cells
Reinke crystals (Leydig cell tumour)
Renal epithelial casts in urine
Acute toxic/viral nephrosis
Rhomboid crystals, positively bifringent
Pseudogout (calcium pyrophosphate dihydrate)
Rib notching
Coartctation of the aorta
Sheets of medium-sized lymphoid cells ('starry sky' appearance on histology)
Burkitt's lymphoma (t[8; 14] c-myc activation, associated with EBV)
Silver-staining spherical aggregation of tau proteins in neurons
Pick bodies (Pick's disease: progressive dementia, similar to Alzheimer's)
"Soap bubble" in femur or tibia on xray
Giant cell tumour of bone (generally benign)
"Spikes" on basement membrane, "dome-like" endothelial deposits
Membranous glomerulonephritis (may progress to nephrotic syndrome)
Stacks of red blood cells
Rouleaux formation (high ESR, multiple myeloma)
Stippled vaginal epithelial cells
Stippled vaginal epithelial cells
"Clue cells" (Gardnerella vaginalis)
"Tennis-racket"-shaped cytoplasmic organelles (EM) in Langerhans cells
Birbeck granules (histocytosis X: eosinophilic granuloma)
Thrombi made with white/red layers
Lines of Zahn (arterial thrombus, layers of platelets/RBCs)
"Thumb sign" on lateral xray
"Thumb sign" on lateral xray
Epiglottitis (Haemophilus influenza)
Thyroid-like appearance of kidney
Chronic bacterial pyelonephritis
"Tram-track" appearance on LM
Membranoproliferative glomerulonephritis
Triglyceride accumulation in liver cell vacuoles
Fatty liver disease (alcoholic or metabolic syndrome)
WBCs that look 'smudged'
CLL (almost always B cell; affects elderly)
"Wire loop" glomerular appearance on LM
Lupus nephropathy
Yellow CSF
Xanthochromia (subarachnoid hemorrhage)