• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/441

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

441 Cards in this Set

  • Front
  • Back
Abdominal pain, ascites, hepatomegaly
Budd-Chiari syndrome (posthepatic venous thrombosis)
Achilles tendon xanthoma
Familial hypercholesterolemia ( .l. LDL receptor signaling)
Adrenal hemorrhage, hypotension, DIC
Waterhouse-Friderichsen syndrome (meningococcemia)
Arachnodactyly, lens dislocation, aort · c dissection, hyperflexible joints
Marfan's syndrome (fibrillin defect)
Athlete with polycythemia .
Erythropoietin injection
Back pain, fever, night sweats, weight loss
Pott's disease (vertebral tuberculosis)
Bilateral hilar adenopathy, uveitis
Sarcoidosis (noncaseating granulomas)
Blue sclera
Osteogenesis imperfecta (collagen defect)
Bluish line on gingiva
Burton's line (lead poisoning)
B one pain, bone enlargement, arthritis
Paget's disease of bone (1' osteoblastic and osteoclastic activity)
Bounding pulses, diastolic heart murmur, head bobbing
Aortic regurgitation
Butterfly facial rash and Raynaud's phenomenon in a young female
Systemic lupus erythematosus
Cafe-au-lait spots, Lisch nodules (iris hamartoma)
Neurofibromatosis type I (+ 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's) : X-linked recessive deletion of dystrophin gene
Cherry-red spot on macula
Tay-Sachs (ganglioside accumulation) or Niemann-Pick (sphingomyelin accumulation), central retinal artery occlusion
Chest pain on exertion
Angina (stable: moderate exertion; unstable: minimal exertion)
Chest pain, pericardia! 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
Cowers' sign (Duchenne muscular dystrophy)
Child with fever develops red rash on face that spreads to body
Slapped cheeks (erythema infectiosum/fifth disease : parvovirus B 19)
Chorea, dementia, caudate degeneration
Huntington's disease (autosomal-dominant CAG repeat expansion)
Chronic exercise intolerance with myalgia, fatigue, painful cramps, myoglobinuria
McArdle's disease (muscle glycogen phosphorylase deficiency)
Cold intolerance
Hypothyroidism
Conjugate lateral gaze palsy, horizontal diplopia
Internuclear ophthalmoplegia (damage to MLF; bilateral [multiple sclerosis] , unilateral [stroke))
Continuous "machinery" heart murmur
PDA (close with indomethacin; open with misoprostol
Cutaneous/dermal edema due to connective tissue deposition
Myxedema (caused by hypothyroidism, Graves' disease I periorbital!)
Dark purple skin/mouth nodules
Kaposi's sarcoma (usually AIDS patients [gay men]: associated with HHV-8)
Deep, labored breathing/hyperventilation
Kussmaul breathing (diabetic ketoacidosis)
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 squamous cell carcinoma)
Elastic skin, hypermobility of joints
Ehlers-Danlos syndrome (type III collagen defect)
Enlarged, hard left supraclavicular node
Virchow's node (abdominal metastasis)
Erythroderma, lymphadenopathy, hepatosplenomegaly, atypical T cells
Sezary syndrome (cutaneous T-cell lymphoma) or mycosis fungoides
Facial muscle spasm upon tapping
Chvostek's sign (hypocalcemia)
Fat, female, forty, and fertile
Acute cholelithiasis (bile duct blockage)
Fever, chills, headache, myalgia following antibiotic treatment for syphilis
Jarisch-Herxheimer reaction (rapid lysis of spirochetes resultsin toxin release)
Fever, cough, conjunctivitis, coryza, diffuse rash
Measles (Morbilli virus)
Fever, n ight sweats, weight loss
B symptoms (lymphoma)
F ibrous plagues in soft tissue of penis
Peyronie's disease (connective tissue disorder)
Gout, mental retardation, self-mutilating behavior in a boy
Lesch-Nyhan syndrome (HGPRT deficiency, X-linked recessive)
Green-yellow rings around peripheral cornea
Kayser-F leischer 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 symptoms
Gaucher's disease (glucocerebrosidase deficiency)
Hereditary nephritis, sensorineural hearing loss, cataracts
Alport syndrome (mutation in a chain of collagen IV)
Hypercoagulability (leading to migrating DVTs and vasculitis)
Trousseau's sign (adenocarcinoma of pancreas or lung)
Hyperphagia, hypersexuality, hyperorality, hyperdocility
KlLiver-Bucy syndrome (bilateral amygdala lesion)
Hyperreflexia, hypertonia, positive Babinski sign
UMN damage
Hypertension, hypokalemia, metabolic alkalosis
Conn's syndrome
Hyporeflexia, hypotonia, atrophy
LMN damage
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 hypoglycemia, failure to thrive, and hepatomegaly
Cori's disease (debranching enzyme deficiency)
Infant with microcephaly, rocker-bottom feet, clenched hands, and structural heart defect
Edwards' syndrome (trisomy 18)
Keratin pearls on a skin biopsy
Squamous cell carcinoma
Large rash with bull's-eye appearance
Erythema chronicum migrans from Ixodes tick bite (Lyme disease: Borrelia)
Lucid interval after traumatic brain injury
Epidural hematoma (middle meningeal artery rupture)
Male child, recurrent i nfections, no mature B cells
Bruton's disease _0-linked agamm??glob??linei_nia)
Mucosal bleeding and prolonged bleeding time
Glanzmann's thrombasthenia (defect in platelet aggregation due to lack of Gpllb/Illa)
Multiple colon polyps, osteomas/soft tissue tumors, impacted/ supernumerary teeth
Gardner's syndrome (subtype of FAP)
Myopathy (infantile hypertrophic cardiomyopathy), exercise intolerance
Pompe's disease (lysosomal a-1 ,4-glucosidase deficiency)
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, bilateral internuclear ophthalmoplegia
Multiple sclerosis
Oscillating slow/fast breathing
Cheyne-Stokes respirations (central apnea in CHF or I intracranial pressure)
Painful blue fingers/toes, hemolytic anemia
Cold agglutinin 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 the pancreatic head obstructing bile duct
Palpable purpura on buttocks/legs, joint pain, abdominal pain (child)
Henoch-Schonlein purpura (IgA vasculitis affecting skin and kidneys)
Pancreatic, pituitary, parathyroid tumors
MEN 1 (autosomal dominant)
Pink complexion, dyspnea, hyperventilation
Pink puffer (emphysema: centroacinar [smoking] , par??a0nar [ C?-r!??titrrr??in defic??r??cy])
Polyuria, acidosis, growth failure, electrolyte imbalances
Fanconi's syndrome (proximal tubular reabsorption defect)
Positive anterior "drawer sign"
Anterior cruciate ligament (ACL) 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 demyel i nating polyneuropathy)
Rash on palms and soles
Coxsackie A, zo syphilis, Rocky Mountain spotted fever
Recurrent colds, unusual eczema, high serum IgE
Hyper-IgE syndrome (Job's syndrome: neutrophil chemotaxis abnormality)
Red "currant jelly" sputum in alcoholic or diabetic patients
Klebsiella pnewnoniae
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 hemoglobinuria
Renal cell carcinoma (bilateral), hemangioblastomas, angiomatosis, pheochromocytoma
von Hippel-Lindau disease (dominant tumor suppressor gene mutation)
Resting tremor, rigidity, akinesia, postural instability
Parkinson's disease (nigrostriatal dopamine depletion)
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, i incidence of tumors/leukemia, aplastic anemia
Fanconi's anemia (genetic loss of DNA crosslink repair; often progresses to AML)
Single palm crease
Simian crease (Down syndrome)
S itus inversus, chronic sinusitis, bronchiectasis, infertility
Kartagener's syndrome ( dynein arm defect affecting cilia)
Skin hyperpigmentation
Addison's disease (l o adrenocortical insufficiency causes i ACTH and a-MSH production)
Slow, progressive muscle weakness in boys
Becker's muscular dystrophy (X-linked missense mutation in dystrophin; less severe than Duchenne's)
Small, irregular red spots on buccal/lingual mucosa with blue-white centers
Koplik spots (measles; rubeola virus)
Smooth, flat, moist white lesions on genitals
Condylomata lata (2° syphilis)
Splinter hemorrhages in fingernails
Bacterial endocarditis
Strawberry tongue
Scarlet fever, Kawasaki disease, toxic shock syndrome
Streak ovaries, congenital heart disease, horseshoe kidney, cystic hygroma at birth
Turner syndrome (45XO, 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 coll agen 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 tumors, pheochromocytoma
MEN 2A (autosomal dominant ret mutation)
Thyroid tumors, pheochromocytoma, ganglioneuromatosis
MEN 2B (autosomal dominant ret mutation)
Toe extension/fanning upon plantar scrape
Babinski sign (UMN lesion)
Unilateral facial drooping involving forehead
Bell's palsy (LMN CN VII palsy)
Urethritis, conjunctivitis, arthritis in a male
Reactive arthritis associated with HLA-B27
Vascular birthmark (port-wine stain)
Hemangioma (benign, but associated with Sturge-Weber syndrome)
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
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 (hydralazine, isoniazid, phenytoin procainamide)
Anti-lgG antibodies
Rheumatoid arthritis (systemic inflammation, joint pannus, boutonniere deformity)
Antimitochondrial antibodies (AMAs)
Primary biliary cirrhosis (female, cholestasis, portal hypertension)
Antineutrophil cytoplasmic antibodies (ANCAs)
Vasculitis (c-ANCA: Wegener's; p-ANCA: microscopic polyangiitis, Churg-Strauss syndrome)
Antinuclear antibodies (ANAs : anti-Smith and anti-dsDNA)
SLE (type Ill hypersensitivity)
Antiplatelet antibodies
Idiopathic thrombocytopenic purpura (ITP)
Anti-topoisomerase antibodies
Diffuse systemic scleroderma
Anti-transglutaminase/anti-gliadin/anti-endomysial antibodies
Celiac disease (diarrhea, d istention, weight loss)
Apple core lesion on abdominal x-ray
Colorectal cancer (usually left-sided)
Azurophilic granular needles in leukemic blasts
Auer rods (acute myelogenous leukemia, 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 tap on LP
Subarachnoid hemorrhage
Boot-shaped heart on x-ray
Tetralogy of Fallot, RVH
Branching gram-positive rods with sulfur granules
Actinomyces israelii
Bronchogenic apical lung tumor
Pancoast tumor (can compress sympathetic ganglion and cause Horner's syndrome)
Brown tumor of bone
Hemorrhage (hemosiderin) causes brown color of osteolytic cysts. Due to: l. 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 of ovary
Endometriosis (frequently involves both ovaries)
Circular grouping of dark tumor cells surrounding pale neurofibril
Homer Wright rosettes (neuroblastoma, medulloblastoma, retinoblastoma)
Colonies of mucoid Pseudomonas in lungs
Cystic fibrosis (AR mutation to CFTR resulting in fat-soluble vitamin deficiency and mucous plugs)
Decreased a-fetoprotei n in amniotic fluid/maternal serum
Down syndrome or other chromosomal abnormality
Degeneration of dorsal column nerves
Tabes dorsalis W syphilis)
Depigmentation of neurons in substantia nigra
Parkinson's disease (basal ganglia disorder: rigidity, resting tremor, bradykinesia)
Desquamated epithelium casts in sputum
Curschmann's spirals (bronchial asthma; can result in whorled mucous plugs)
Disarrayed granulosa cells in eosinophilic fluid
Call-Exner bodies (granulosa-theca cell tumor of the ovary)
Dysplastic squamous cervical cells with nuclear enlargement and hyperchromasia
Koilocytes (HPV: predisposes to cervical cancer)
Enlarged cells with intranuclear inclusion bodies
Owl's-eye appearance of CMV
Enlarged thyroid cells with ground-glass nuclei
Orphan Annie eye nuclei (papillary carcinoma of the thyroid)
Eosinophilic cytoplasmic inclusion i n liver cell
Mallory bodies (alcoholic liver disease)
Eosinophilic cytoplasmic inclusion in nerve cell
Lewy body (Parkinson's disease)
Eosinophilic globule in liver
Councilman body (toxic or 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-Sternberg cells ( Hodgkin's lymphoma)
Glomerulus-like structure surrounding vessel in germ cells
Schiller-Duval bodies (yolk sac tumor)
Hair-on-end (crew-cut) appearance on x-ray
P-thalassemia, sickle cell anemia (marrow expansion)
hCG elevated
Choriocarcinoma, hydatidiform mole (occurs with and without embryo)
Heart nodules (granulomatous)
Aschoff bod ies (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, pulmonary embolism, DIC
Hilar lymphadenopathy, peripheral granulomatous lesion in middle or lower lung lobes (can calcify)
Chon complex W TB : Mycobacterium bacilli)
Honeycomb lung on x-ray
Interstitial fibrosis
Hypersegmented neutrophils
Megaloblastic anemia (B12 deficiency: neurologic symptoms; folate deficiency: no neurologic symptoms)
Hypochromic, microcytic anemia
Iron deficiency anemia, lead poisoning, thalassemia (HbF sometimes present)
Increased a-fetoprotein in amniotic fluid/maternal serum
Dating error, anencephaly, spina bifida (neural tube defects)
Increased uric acid levels
Gout, Lesch-Nyhan syndrome, tumor lysis syndrome, loop and thiazide diuretics
Intranuclear eosinophilic droplet-like bodies
Cowdry type A bodies (HSV or CMV)
Iron-contai ning nodules in alveolar septum
Ferruginous bodies (asbestosis: t chance of mesothelioma)
Large lysosomal vesicles in phagocytes, immunodeficiency
Chediak-Higashi disease (congenital failure of phagolysosome formation)
Lead pipe appearance of colon on x-ray
Ulcerative colitis (loss of haustra)
Linear appearance of glomeruli on immunofluorescence
Goodpasture's syndrome
Low serum ceruloplasmin
Wilson's disease (hepatolenticular degeneration)
Lumpy-bumpy appearance of glomeruli on immunofluorescence
Poststreptococcal glomerulonephritis (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 (called the 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 (lgM)
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 birefringent crystals
Gout (monosodium urate crystals)
Nodular hyaline deposits in glomeruli
Kimmelstiel-Wilson nodules (diabetic nephropathy)
Novobiocin response
Sensitive: Staphylococcus epidermidis; resistant: Staphylococcus saprophyticus
Nutmeg appearance of liver
Chronic passive congestion of liver clue to right heart failure
Onion-skin periosteal reaction
Ewing's sarcoma (malignant round-cell tumor)
Optochin response
Sensitive: Streptococcus pneumoniae; resistant: Viridans streptococcus
Periosteum raised from bone, creating triangular area
Cadman's triangle on x-ray (osteosarcoma, Ewing's sarcoma,pyogenic osteomyelitis)
Poclocyte fusion on EM
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 protein tau
Neurofibrillary tangles (Alzheimer's disease and CJD)
Pseudopalisading tumor cells on brain biopsy
Glioblastoma multiforme
RBC casts in urine
Acute glomerulonephritis
Rectangular, crystal-like, cytoplasmic inclusions in Leydig cells
Reinke crystals (Leydig cell tumor)
Renal epithelial casts in urine
Acute toxic/viral nephrosis
Rhomboid crystals, positively birefringent
Pseudogout (calcium pyrophosphate dihydrate)
Rib notching
Coarctation of the aorta
Ring-enhancing brain l esion in AIDS
Toxoplasma gondii
Sheets of medium-sized lymphoid cells ( "starry sky"appearance on histology)
Burkitt's lymphoma (t[8: 14) c-myc activation, associated with EBV; "black sky" made up of malignant cells)
Silver-staining spherical aggregation of tau proteins inneurons
Pick bodies ( Pick's 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 glomerulonephritis (may progress to nephrotic syndrome)
Stacks of red blood cells
Rouleaux formation (high ESR, multiple myeloma)
Stippled vaginal epithelial cells
Clue cells ( Gardnerella vagina lis)
Tennis-racket-shaped cytoplasmic organelles (EM) in Langerhans cells
Birbeck granules (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 (Haemophilus influenzae)
Thyroid-like appearance of kidney
Chronic bacterial pyelonephritis
Tram-track appearance on LM
M-embranop-roliferative glomerulonephritis
Triglyceride accumulation in liver cell vacuoles
Fatt-y liver d-isease (alcoholic or metabolic syndrome)
WBCs that look "smudged"
C-LL -(alm-ost always B cell; affects the elderly)
Wire loop glomerular appearance on LM
Lupus nephropathy
Yellow CSF
Xantho-chromia (previous -s-ubarachnoid hemorrhage)
Absence seizures
Ethosuximide
Acute gout attack
NSAIDs, colchicine
Acute promyelocytic leukemia (M3)
All-trans retinoic acid
ADHD
Methylphenidate, amphetamines
Alcohol abuse
AA +disulfiram for patient and Al-Anon for family
Alcohol withdrawal
Benzodiazepines
Anorexia
SSRis
Anticoagulation during pregnancy
Heparin
Anxiety
Buspirone
Arrhythmia in damaged cardiac tissue
Class IB antiarrhythmic (lidocaine, mexiletine, tocainide)
B1z deficiency
B12
Benign prostatic hyperplasia
Tamsulosin, finasteride
Bipolar disorder
Lithium, valproate, carbamazepine (mood stabilizers)
Breast cancer in postmenopausal woman
Aromatase inh ibitor
Buerger's disease
Smoking cessation
Bulimia
SSRis
Candida albicans
Amphotericin B (systemic), nystatin (oral thrush, esophagitis)
Carcinoid syndrome
Octreotide
Chlamydia trachomatis
Doxycycline (+ ceftriaxone for gonorrhea coinfection), erythromycin eye drops (prophylaxis in infants)
Chronic gout
Probenecid (underexcretor) , allopurinol (overproducer)
Chronic hepatitis
IFN-a
Chronic myelogenous leukemia
Imatinib
Clostridium botulinum
Antitoxin
Clostridium difficile
Oral metronidazole
Clostridium tetani
Antitoxin + vaccine booster + diazepam
Crohn's disease
Corticosteroids, i nfliximab
Cryptococcus neoformans
Fluconazole (prophylaxis in AIDS patients)
Cystic fibrosis
N-acetylcysteine + antipseudomonal prophylaxis (tobramycin/azithromycin)
Cytomegalovirus
Ganciclovir
Depression
SSRis (first-line)
Diabetes insipidus
Desmopressin (central); hydrochlorothiazide, indomethacin, amiloride (nephrogenic)
Diabetes mellitus type 1
Dietary intervention (low-sugar)+ insulin replacement
Diabetes mellitus type 2
Dietary intervention, oral hypoglycemic, and insulin (possible)
Diabetic ketoacidosis
Fluids, insulin, K+
Enterococci
Vancomycin/ampicillin + aminoglycoside
Erectile dysfunction
Sildenafil
ER-positive breast cancer
Tamoxifen
Ethylene glycol/methanol intoxication
Fomepizole (alcohol dehydrogenase inhibitor)
Folate deficiency
Folate
Haemophilus influenzae (B)
Rifampin (prophylaxis)
Hemorrhagic cystitis
Mesna
Heparin toxicity (acute)
Protamine sulfate
HER2/neu-positive breast cancer
Trastuzumab
Hyperaldosteronism
Spironolactone
Hypercholesterolemia
Statin (first-line)
Hypertriglyceridemia
Fibrate
Immediate anticoagulation
Heparin
Infertility
Leuprolide, GnRH (pulsatile)
Influenza
Amantadine/rimantadine
Legionella pneumophila
Erythromycin
Long-term anticoagulation
Warfarin
Malaria
Chloroquine/mefloquine (for blood schizont), primaquine (for liver hypnozoite)
Malignant hyperthermia
Dantrolene
Medical abortion
Mifepristone
Migraine
Sumatriptan
MRSA
Vancomycin
Multiple sclerosis
Beta-interferon
Mycobacterium tuberculosis
RIPES (rifampin, INH, pyrazinamide, ethambutol,streptomycin)
Neisseria gonorrhoeae
Ceftriaxone (add doxycycline to cover likely concurrent Chlamydia)
Neisseria meningitidis
Penicillin/ceftriaxone, rifampin (prophylaxis)
Neural tube defect prevention
Folate
Osteomalacia/rickets
Vitamin D supplementation
Patent ductus arteriosus
Indomethacin
Pheochromocytoma
a-antagonists
Pneumocystis jiroveci
TMP-SMX (prophylaxis in AIDS patient)
Prolactinoma
Bromocriptine (dopamine agonists)
Prostate cancer/uterine fibroids
Leuprolide, GnRH (continuous)
Prostate carcinoma
Flutamide
Pseudomonas aeruginosa
Antipseudomonal penicillin + aminoglycoside
Pulmonary hypertension
Bosentan
Rickettsia rickettsii
Tetracycline, chloramphenicol (especially in context of aplastic anemia)
Ringworm infections
Terbinafine, griseofulvin, imidazole
Schizophrenia (negative symptoms)
5 -HT2A antagonists (e.g., olanzapine)
Schizophren ia (positive symptoms)
D2 receptor antagonists
SIADH
Demeclocycline, lithium
Sickle cell anemia
Hydroxyurea (t HbF )
Sporothrix schenckii
Oral KI
Stable angina
Sublingual nitroglycerin
Staphylococcus aureus
Methicillin/naficillin
Streptococcus bovis
Penicillin prophylaxis
Streptococcus pneumoniae
Penicillin/cephalosporin (systemic infection, pneumonia), vancomycin (meningitis)
Streptococcus pyogenes
Penicillin prophylaxis
Temporal arteritis
High-dose steroids
Tonic-clonic seizures
Phenytoin, valproate, carbamazepine
Toxoplasma gondii
Sulfonamide + pyrimethamine
Treponema pallidum
Penicillin
Trichomonas vaginalis
Metronidazole (patient and partner)
Ulcerative colitis
5-ASA, infliximab
UTI prophylaxis
TMP-SMX
Warfarin toxicity
Fresh frozen plasma (acute), vitamin K (chronic)
Wegener's granulomatosis
Cyclophosphamide, corticosteroids
Actinic (solar) keratosis
Precursor to squamous cell carcinoma
Acute gastric ulcer associated with CNS injury
Cushing's ulcer (t ICP stimulates vagal gastric secretion)
Acute gastric ulcer associated with severe burns
Curling's ulcer (greatly reduced plasma volume results in sloughing of gastric mucosa)
Alternating areas of transmural inflammation and normal colon
Skip lesions (Crohn's disease)
Aneurysm, dissecting
Hypertension
Aortic aneurysm, abdominal and descending aorta
Atherosclerosis
Aortic aneurysm, ascending
Marfan's syndrome (idiopathic cystic medial degeneration)
Atrophy of the mammillary bodies
Wernicke's encephalopathy (thiamine deficiency causing ataxia, ophthalmoplegia, and confusion)
Autosplenectomy (fibrosis and shrinkage)
Sickle cell anemia ( HbS)
Bacteria associated with gastritis, peptic ulcer disease, and 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 two decades)
Bleeding disorder with Gplb deficiency
Bernard-Soulier disease (defect in platelet adhesion to von Willebrand's factor)
Brain tumor (adults)
Supratentorial: mets > astrocytoma (including glioblastoma multiforme) >meningioma> schwannoma
Brain tumor (kids)
Infratentorial: medulloblastoma (cerebellum) or supratentorial : craniopharyngioma (cerebrum)
Breast cancer
Infiltrating ductal carcinoma (in the United States, l in 9 women will develop breast cancer)
Breast mass
1. Fibrocystic change 2. Carcinoma (in postmenopausal women)
Breast tumor (benign)
Fibroadenoma
Cardiac Primary tumor (kids)
Rhabdomyoma, often seen in tuberous sclerosis
Cardiac manifestation of lupus
Libman-Sacks endocarditis (nonbacterial, affecting both sides of mitral valve)
Cardiac tumor (adults)
1. Metastasis 2 . 1° myxoma (4:lleft 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
Compression fracture
Osteoporosis (type I : postmenopausal woman; type II: elderly man or woman)
Congenital adrenal hyperplasia, hypotension
2 1-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
Tuberculosis (developing world) ; systemic lupuserythematosus (developed world)
Coronary artery involved in thrombosis
LAD > RCA > LCA
Cretinism
Iodine deficit/hypothyroidism
Cushing's syndrome
l. Corticosteroid therapy 2. Excess ACTH secretion by pituitary 3. Small cell lung carcinoma
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 i n SLE
Lupus nephropathy
Dementia
l . 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 d iverticulum (diagnosed by barium swallow)
Ejection click
Aortic /pulmonic stenosis
Esophageal cancer
Squamous cell carcinoma (worldwide) ; adenocarcinoma (U.S.)
Food poisoning (exotoxin mediated)
S. aureus, B. cereus
Glomerulonephritis (adults)
Berger's disease (IgA nephropathy)
Gynecologic malignancy
Endometrial carcinoma (most common in U. S.); cervical carcinoma (most common worldwide)
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 (U.S.)
1. Enterobius vermicularis 2. Ascaris lumbricoides
Hematoma- epidural
Rupture of middle meningeal artery (trauma; lentiform shaped)
Hematoma-subdural
Rupture of bridging veins (crescent shaped)
Hemochromatosis
Multiple blood transfusions or hereditary HFE mutation (can result in CHF, "bronze diabetes," and i risk of hepatocellular carcinoma)
Hepatocellular carcinoma
Cirrhotic liver (associated with hepatitis B and C)
Hereditary bleeding disorder
von Willebrand's disease
Hereditary harmless jaundice
Gilbert's syndrome (benign congenital unconjugated hyperbilirubinemia)
HLA-B27
Ankylosing spondylitis, Reiter's syndrome, ulcerative colitis, psonas1s
HLA-DR3 or -DR4
Diabetes mellitus type l, rheumatoid arthritis, SLE
Holosystolic murmur
VSD, tricuspid regurgitation, mitral regurgitation
Hypercoagulability, endothelial damage, blood stasis
Virchow's triad (results in venous thrombosis)
Hypertension, 2°
Renal disease
Hypoparathyroidism
Accidental excision during thyroidectomy
Hypopituitarism
Pituitary adenoma (usually benign tumor)
Infection 2° to blood transfusion
Hepatitis C
Infections in chronic granulomatous disease
Staphylococcus aureus, E. coli, Aspergillus (catalase positive)
Kidney stones
l . Calcium = radiopaque 2. Struvite (ammonium) = radiopaque (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 tumor
Basal cell carcinoma (rarely metastasizes)
Mental retardation
l . Down syndrome 2. Fragile X syndrome
Metastases to bone
Breast, lung, thyroid, testes, prostate, kidney
Metastases to brain
Lung, breast, skin (melanoma) , kidney (renal cell carcinoma) , GI
Metastases to liver
Colon, gastric, pancreatic, breast, and lung carcinomas
Mitochondrial inheritance
Disease occurs in both males and fem ales, inherited through females only
Mitral valve stenosis
Rheumatic heart disease
Mixed (UMN and LMN) motor neuron disease
ALS
Myocarditis
Coxsackie B
Neoplasm (kids)
l . ALL 2. Cerebellar medulloblastoma
Nephrotic syndrome (adults)
Focal segmental glomerulosclerosis
Nephrotic syndrome (kids)
Minimal change disease (associated with infections/vaccinations; treat with corticosteroids)
Neuron m igration failure
Kallmann syndrome
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
Salmonella
Osteomyelitis with IV drug use
Pseudomonas, S. aureus
Ovarian metastasis from gastric carcinoma or breast cancer
Krukenberg tumor (mucin-secreting signet-ring cells)
Ovarian tumor (benign, bilateral)
Serous cystadenoma
Ovarian tumor (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 30-60
Pelvic inflammatory disease
Neisseria gonorrhoeae (monoarticular arthritis)
Philadelphia chromosome t(9;22) (bcr-abl)
CML (may sometimes be associated with ALL/AML)
Pituitary tumor
I. Prolactinoma 2. Somatotropic "acidophilic" adenoma
Primary amenorrhea
Turner syndrome (45XO)
Primary bone tumor (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, alpha1 antitrypsin)
Pulmonary hypertension
COPD
Recurrent inflammation/thrombosis of small/medium vessels in extremities
Buerger's disease (strongly associated with tobacco)
Renal tumor
Renal cell carcinoma: associated with von Hippel-Lindau
and adult polycystic kidney disease; paraneoplastic syndromes
(EPO, renin, PTH, ACTH)"
Right heart failure due to a pulmonary cause
Cor Pulmonale
S3 (protodiastolic gallop)
increased ventricular filling (L -7 R shunt, mitral regurgitation, LV failure [CHF])
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 fusion)
Temporal arteritis
Risk of ipsilateral blindness clue to thrombosis of ophthalmic artery; polymyalgia rheumatica
Testicular tumor
Seminoma
Thyroid cancer
Papillary carcinoma
Tumor in women
Leiomyoma (estrogen dependent, not precancerous)
Tumor of infancy
Hemangioma (usually regresses spontaneously by childhood)
Tumor of the adrenal medulla (adults)
Pheochromocytoma (usually benign)
Tumor 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, Staphylococcus saprophyticus (young women)
Viral encephalitis affecting temporal lobe
H SV-l
Vitamin deficiency (U. S .)
Folic acid (pregnant women are at high risk; body stores only 3- to 4-month supply; prevents neural tube defects)