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444 Cards in this Set
- Front
- Back
2yo M with recurrent infections and eczema. Workup reveals thrombocytopenia.
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Wiscott Aldrich. X-linked.
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70yo white M with easy bruising, visual disturbance, and elevated IgM
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Waldenstrom's macroglobulinemia
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12yo M with bleeding, elevated PTT, and reduced quantitative factor VIII level. Platelets do no aggregate with ristocetin test.
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von Willebrand's disease
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23yo HIV positive F recently started SMX-TMP with rash, confusion, fever, anemia, thrombocytopenia, tachycardia.
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TTP
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6yo F with itching, joint pain, skin rash who received penicillin six days previously for strep infection.
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Serum sickness (Type III hypersens.)
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62yo Jewish M with pruritus, melena, epistaxis, and history of DVTs.
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Polycythemia vera (itching, epistaxis) Treat with phlebotomy, hydroxyurea for myelosuppression, aspirin for DVT prophy. Risk = develop CML, AML, myelofibrosis.
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12yo M with bony-hard swelling above knee.
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Osteosarcoma
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53yo M with painless lumps in neck, fever, weight loss.
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Non-Hodgkin's lymphoma
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54yo M with fatigue, splenomegaly, anemia, and 'dry tap' on bone marrow biopsy
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Myelofibrosis with myeloid dysplasia
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64yo black M with bone pain, fatigue, and recurrent URIs
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Multiple myeloma
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24yo M with painless lump in neck and CXR with hilar masses.
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Hodgkin's.
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8yo M with palpable rash, hematuria, and joint pain. CBC reveals normal platelet count.
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Henoch-Schonlein Purpura. Small vessel vasculits. IgA deposits. Hemmorhagic urticaria with fever, arthralgias, GI and renal involvement. Associated with URIs.
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21yo F with sudden onset bruisability, edema, and rash following diarrheal illness. Low platelet count.
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HUS
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61yo M with mycobacterium avium infection, splenomegaly, and leukocytes with cytoplasmic projections seen on CBC.
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Hairy cell leukemia (B cell)
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45yo M with fever, rash, diarrhea, and jaundice. Elevated IgE level and history of leukemia.
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Graft-versus-host
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45yo M with frank rigors 1hr following blood transfusion.
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Febrile nonhemolytic transfusion rxn
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25yo F with continued bleeding following delivery.
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DIC
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55yo M with no complaints, found on physical exam to have splenomegaly and leukocytosis.
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CML
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65yo M with lymphadenopathy, hepatosplenomegaly, and leukocytosis with smudge cells.
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CLL
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66yo M with CLL has urine that gets darker during the day.
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autoimmune hemolytic anemia
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18yo M with pallor, petechiae, and recurrent URIs
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aplastic anemia
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25yo F with recent infection, gingival hyperplasia, and leukocytosis with bone marrow expansion.
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AML
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43yo M with epigastric pain and diarrhea refractory to medical management.
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ZE syndrome
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40yo F with intellectual impairment, jaundice, and choreiform movements.
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Wilson's
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37yo M with acute pain in anorectal area and BRBPR for 4 months.
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thrombosed ext. hemorrhoid
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45yo F with pruritus, fatigue, and jaundice.
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PBC
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33yo M with four months epigastric pain radiating to back relieved by eating and leaning forward.
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posterior duodenal ulcer
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36yo F with difficulty swallowing and craving for ice. Physical exam reveals angular stomatitis and glossitis.
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Plummer-Vinson syndrome.
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24yo F with crampy abdominal pain and dark spots on lips.
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Peutz-Jehghers. Multiple polyposis of small intestine, pigmented melanin macules on oral mucosa. Associated with gynecological cancers, but actually a low to moderate colon CA risk.
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51yo M with 4 months pruritus, jaundice, and abdominal pain. Recent 15 pound wt loss.
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pancreatic CA (CEA, CA19-9)
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65yo M with abdominal pain, nausea, vomiting, and diarrhea. Has been suffering abd. Pain 30 min after eating.
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ischemic bowel
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50yo M with EtOH cirrhosis develops oliguria and abdominal distenstion.
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hepatorenal
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65yo M alcoholic with RUQ pain, jaundice, anorexia, and distention worsening over two months.
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hepatocellular carcinoma
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40yo M with increased pigmentation. PE reveals cardiomegaly. UA reveals glycosuria.
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hemochromatosis (cirrhosis, bronze diabetes, heart failure)
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24yo F found on dental checkup to have supernumerary teeth. Has father with history of colon polyps and
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Gardener's syndrome.
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44yo M with hematemesis and melena. Has had recurrent painless hematemesis for several years.
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gastric leiomyoma (#1 benign tumor of stomach)
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83yo M with epigastric pain, anorexia, and frequent vomiting. Guaic positive stools. Palpable mass over L shoulder.
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gastric CA (atrophic gastritis, pernicious anemia, ulcers, type A blood = risk; Krukenberg tumor = retro peritoneal spread to ovaries.
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68yo F smoker with dysphagia.
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esophageal CA (squamous > adeno in distal third)
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54yo F with colicky LLQ pain and bloody stools that have returned intermittently over several months.
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diverticulitis
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45yo M with recurrent epigastric pain that radiates to back and foul-smelling stools.
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chronic pancreatitis (alcoholism, cystic fibrosis)
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25yo F with diarrhea, foul smelling stools, pruritus, dry skin, and bruising.
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celiac disease (anti-gliadin Ab, nutrient malabsorption)
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67yo F with several months fatigue, weight loss, intermittent diarrhea with palpable RLQ mass.
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cecal CA (anemia and + guaic test + virchow's node)
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52yo M with diarrhea and facial flush.
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carcinoid = primary GI tumors arise from neuroendocrine cells "Kulchitsky cells" and secrete 5-HT, histamine, gastrin, and prostaglandins. Malignant or benign.
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45yo M with AIDS now with painful swallowing.
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candida esophagitis (candida, rx with oral fluconazole)
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34yo M with mediepigastric pain, periumbilical/flank bruising, and hypotension.
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acute pancreatitis (Cullen's / Grey Turner's sign, assoc. with gallstones and alcohol)
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33yo F with substernal pain and difficulty swallowing. Sometimes regurgitates food.
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achalasia (loss of ganglion cells in Auerbach's plexus). Esophageal CA risk. Can arise from Chagas disease (also with cardiomyopathy).
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50yo F with cold nodule in the neck. Normal TSH, T3 and T4.
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thyroid CA (risk = ionizing rad - papillary CA c best prognosis, also follicular, mixed, and medullary assoc c MENIIa and IIb) psammoma bodies on FNA.
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30yo F with weight loss, 2yrs amenorrhea following delivery of healthy baby.
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Sheehan's (postpartum pituitary infarction) decreased levels of all trophic hormones, can occur in males and nonpregnant females following trauma, SS anemia, DIC, and stroke)
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33yo F with menstrual irregularity and milky nipple discharge.
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prolactinoma (most common pituitary adenoma; GnRH suppressed by excessive prolactin, reduces LH and estradiol. In males = HA, impotence, visual disturbance.
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56yo F with flank pain, confusion, constipation, thirst and polyuria.
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hyperparathyroidism (symptoms of hypercalcemia, bank keratopathy, cystic bone lesions = osteitis fibrosa cystica, adenoma = 1 gland, hyperplasia = 4 gland, renal stones, elevated serum Ca and AP with lowPO4.
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42yo F with hypertension, weakness, and decreased urinary volume.
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Conn's (hypokalemia, hypernatremia, hypertension, increased urinary aldosterone, low plasma renin). Usually adrenal cortex adenoma, sometimes adrenal cortical hyperplasia.
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53yo F with fatigue, insomnia, depresison. Thinning of skin, hirsutism, vaginal atrophy.
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menopause (hot flashes, vaginal atrophy, osteoporosis). Post-menopausal bleeding gets biopsy to r/o endometrial cancer.
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48yo F with weakness, lethargy, cold intolerance.
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hypothyroidism (weight gain, constipation, coarsening of facial features, hair loss, hoarseness, depression, loss of outer third of eyebrows, delayed recovery phase of achilles. Most common = Hashimoto's
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46yo M with impotence, fatigue and decreased peripheral vision. Is also hypotensive.
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hypopituitarism: Low FSH, LH, TSH, ACTH. Most common cause adenoma compressing anterior pituitary.
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29yo F with seizure. Has history of thyroid surgery two years ago.
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hypoparathyroidism (circumoral and foot numbness, fasciculations, chvostek's sign, trousseau's sign, brittle nails, low serum calcium, elevated PO4, low Mg, low PTH. Most commonly d/t thyroidectomy, symptoms d/t hypocalcemia.
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24yo F with weight loss despite good appetite, anxiety, menstrual irregularity, and tremors.
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hyperthyroidism = diarrhea, heat intolerance, palpitations, tremors, increased T4, decr. TSH. Hot nodule with decreased uptake in surrounding tissue and other lobe d/t atrophy of remainder of gland. Rx with propranolol, PTU, methimazole.
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45yo F with anterior neck fatigue, history of RA, and cold intolerance.
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Hashimoto's (anti-thyroglobulin and antimicrosomal Abs, often assoc with other autoimmune dx including SLE, pernicious anemia, Sjogren's, hepatitis, HLA-DR5/3. May see thyrotoxicosis early during disease course.
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55yo M with obesity, thirst, and excessive appetite.
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DM2. Can develop nonketotic hyperosmoler coma but not DKA.
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44yo F with irritability, easy bruising, weight gain, and glucosuria.
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Cushing's (truncal obesity, moon facies, buffalo hump, hirsutism. Elevated plasma cortisol with high ACTH, hypokalemia, leukopenia, osteoporosis, adrenocortical hyperplasia and pituitary adenoma.
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60yo M with rash composed of red plaques with scaling and nodules. Has not responded to steroid rx.
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Mycosis fungoides. Malignant cutaneous helper T-cell lymphoma; disseminated disease with exfoliative dermatitis and lymphadenopathy = Sezary syndrome. "Red man's disease". CBC shows lymphocytosis.
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68yo outdoor construction worker, raised bleeding lesion over upper lip.
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basal cell carcinoma. Most common skin cancer. Light-skinned people. Sun-exposed areas, slow growing, metastatic disease rare. Increased incidence in xeroderma pigmentosum.
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60yo farmer with skin lesions on forehead, upper lip, dorsum of hands. Scaly rough plaques.
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actinic keratosis. Most common precancerous dermatosis --> squamous cell CA. Signs that preceed malignancy include elevation, ulceration, inflammation, and enlargement >1 cm.
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35yo M with cramping in calves with walking, smokes 3 ppd. PE reveals pallor and cyanosis of distal extremities.
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thromboangiitis obliterans = occluded small and medium arteries, no atherosclerosis, inflammation of all layers of arterial wall. Smoking cessation critical. Amputation may become necessary of fingers/toes.
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79yo F with unilateral HA, jaw pain, visual disturbance in ipsilateral eye.
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temporal arteritis. Most common vasculitis in US. Often coexists with polymyalgia rheumatica. Ophthalmic artery occlusion --> blindness. Biopsy positive 60%, so treat on clinical picture with steroids before biopsy.
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50yo M with palpitations and CP. Has had multiple sexual partners. Has diastolic murmur.
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Syphilitic aortitis. Signs include collapsing pulse, wide pulse pressure, LVH with strain, mid-diastolic murmur at apex = Austin-Flint, VDRL / FTA-ABS positive. "Tree bark" calcification of arch and ascending aorta on CXR, tertiary stage syphillis.
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30yo F with HTN and elevated plasma renin.
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Renovascular hypertension. "String-of-pearls" pattern seen on renal angio. +/- renal artery bruit. Mostly fibromuscular dysplasia (young female), atherosclerosis (older male), <5% of all HTN. Rx with ACE-I but contraindicated in bilateral RAS.
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34yo F in 27th week of pregnancy with dyspnea and orthopnea. History of recurrent strep pharyngitis as child.
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Mitral stenosis. Opening snap and mid-diastolic murmur at apex. +/- LVH and a-fib.
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37yo M with fatigue and dyspnea with exertion. Pansystolic murmur at the apex with radiation to the axilla.
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Mitral insufficiency. Common causes: mitral valve prolapase, ischemic papillary muscle, endocarditis, rheumatic. S3 may be present.
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42yo M with CP, headache and confusion. Has history of HTN.
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malignant HTN. Severe diastolic hypertension, papilledema, hematuria, proteinuria, small scarred kidneys. Rx with sodium nitroprusside or IV beta-blockers to prevent end-organ damage due.
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21yo M with DOE and an episode of syncope while playing tennis.
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HCM. Signs = S4, SEM incr by valsalva, decr by squatting. EKG shows LVH. Echo: asymmetrical septal hypertrophy, ant. motion of mitral valve. Rx with beta-blockers, avoid sports, amiodarone may prevent fatal arrythymia, surgical myomectomy.
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29yo F recently delivered baby, now with dyspnea and pedal edema.
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dilated cardiomyopathy. Systolic dysfunction, decr ejection fraction Peripartum period (3 mo.), alcoholism, hypothyroidism, Freidreich's ataxia, previous myocarditis coxsackie B, adriamycin, tricyclic antidepressants, lithium, cyclophosphamide.
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60yo M with COPD with severe dyspnea at rest, bulging neck veins, and peripheral edema.
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cor pulmonale. Right heart failure d/t pulmonary cause, usually COPD. Other causes include pulmonary fibrosis, pneumoconioses, recurrent PE, PPHTN, obesity with sleep apnea, kyposcoliosis.
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24yo M with angina, DOE, occasional fainting, and systolic ejection murmur to right of sternum.
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aortic stenosis. Crescendo-decrescendo SEM, paradoxical splitting. Causes include congenital bicuspid valve, degenerative calcification, rheumatic.
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31yo M with ankylosing spondylitis develops severe SOB.
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aortic insufficiency. Signs include bounding pulse, wide pulse pressure, diastolic decrescendo murmur at left sternal border. Causes include rheumatic, ankylosing spondylitis, marfan's, reiter's, tertiary syphillis.
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35yo M with nonproductive cough and chest pain worse with inspiration, relieved by sitting up.
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pericarditis. +/- friction rub, incr JVP (c inspir = Kussmaul's sx), elevated ESR, CPK-MB nl, diffuse ST elev., pericardial effusion. Coxsackie A/B, TB, staph/strep, amebiasis, actinomycoses, CRF, SLE, scleroderma, RA, CA, MI, trauma.
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25yo F with myalgias and low-grade fevers starting one week after a dental extraction.
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subacute bact. endocarditis. Ass. c rheumatic dx, mvp, etc. AB prophy prevents. Janeway = periph hemmorhage, Osler's = painful, Splinter hem. = subungal linear, Roth's spots = oval retinal. Strep viridans = most common subacute.
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25yo M with SOB and ankle edema following severe URI.
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viral myocarditis. Cocksackie B > Borrelia burdorferi (Lyme), trypanosome cruzi (Chagas), hypersensitivity rxn in SLE or drug rxn, radiation, sarcoidosis. Echo: dilatation c low EF. ASO titers not elevated. ESR elevated.
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35yo M develops pruritus and blistering rash over shins following camping trip.
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Contact dermatitis = type IV hypersensitivity rxn. Papulovesicular rash c oozing and crusting. Rx c topical and systemic corticosteroids. Also occurs with various irritants, diaper rash.
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5yo M with yellow crusty lesions behind the ear and around the mouth.
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impetigo. "honey-colored" lesions. Group A strep. Rx with cephalosporin, pcn, or erythromycin. ASO titer negative. Highly communicable. Staph. aureus superinfection may cause bullous impetigo. Group B strep impetigo in newborns.
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30yo homosexual M with skin eruption on upper limbs, trunk, anogenital areas.
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molluscum contagiousum. Poxvirus. Opportunistic AIDS infection. Painless, pearly-white, dome-shaped, waxy, umbilicated nodules, 2-5mm, palms and soles not affected.
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16yo M with headache, fever, and rash on the palms and soles. Recent camping in North Carolina. UA demonstrates proteinuria and hematuria.
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RMSF. Rash periph. to central, palms/soles, petechial, thrombocytopenia, + Hess' test = Rumpel-Leede phenomena, + Proteus OX19 / OX2 Weil-Felix rxn. Rickettsia rickettsii. Rx tetracycline. Dermacentor wood tick. East coast of US.
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24yo F with extensive denuding of skin and recent skin infection.
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Scalded skin syndrome. Vesicle fluid is sterile. S. aureus on blood culture. Rx IV methicillin or oxacillin. Phage group 2 staph exotoxin.
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30yo M with bilateral circular red eruption in the groin.
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tinea corporis = ringworm. Circular papulosquamous eruption. Hyphae on KOH skin scrapings. Rx clotrimazole, miconazole, ketoconazole cream. Also systemic griseofulvin, keto/itraconazole prn. Tinea capitis = children.
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28yo M treated for UTI develops raised, red, pruritic rash over trunk and limbs.
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urticaria. wheal and flare rxn, "hives". Rx: stop causative agent, H1/2 blockers, calamine lotion, corticosteroids.
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11yo M with jaundice, dark urine, and recent shellfish ingestion.
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Hep A. Hyperbilirubinemia, ALT>AST, +/- AP, incr PT, incr. urine urobilinogen and bili, + IgM Ab to HepA. No infectivity in 3wks. Fecal/oral, bad water. Not chronic. HAV = naked, ssRNA, picorna. Prevent with killed vaccine and immune globulins.
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25yo M with jaundice following needle stick two months ago.
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HBV. Hyperbili, ALT>AST, +/- AP, HBsAg +, IgM anti-HBc + (window period). Liver biopsy = Councilman bodies. 5% progress to chronic c risk cirrhosis and HCC. Long incubation = 3 months. Enveloped DNA hepadna. HBsAg = chronicity.
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30yo M intermittent jaundice for two years following a motorcycle accident.
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HCV. Percutaneous transmission = 90% of cases. >50% progress to chronic, leading to cirrhosis in 20%. PCR test.
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50yo alcoholic with fever, abdominal pain, and progressive distention of abdomen.
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SBP. Ascites fluid leukocyte count >500/cc; PMNs >250 = diagnostic, low protein and glucose, ascites culture may be negative. Rx empirically, then organism-specific if possible. E. coli = most common.
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56yo M with diarrhea for 2 months, arthritis, and weight loss.
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Whipple's disease. Increased fecal fat. Macrocytic, hypochromic anemia. Small bowel biopsy c PAS + macrophages. Gram + actinomycete bacilli in macs. Rx with bactrim or ceftriaxone for 1 year. Tropheryma whippellii. Vitamin malabsorption.
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19yo F with recurrent episodes of periorbital swelling and dyspnea lasting up to 24hrs.
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C1 esterase inhibitor deficiency. Autosomal dominant. Decreased C4= best screening test. Decreased C1 inhibitor (confirmatory test). Decr. C2, but normalC3, normal IgE. Also called hereditary angioedema.
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3yo M with albinism and recurrent infections with recurrent staph and strep infections.
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Chediak-Higashi. Also nystagmus, photophobia. Decreased neutrophil count. Normal platelet count. Large cytoplasmic granules (Giant Lysosomes) in WBCs. Autosomal recessive, defect in microtubule polymerization in leukocytes. Defective chemotaxis.
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2yo M with recurrent fungal and staph furunculosis and neutrophilic leukocytosis.
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Chronic granulomatous disease. X-linked disorder of neutrophils, deficient NADPH oxidase . Normal chemotaxis, degranulation, and phagocytosis. Deficient killing d/t myeloperoxidase system. Recurrent staph infections. Rx SMP-TMP prophy.
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25yo F with recurrent sinusitis, multiple allergies, watery diarrhea, and hypopigmented skin lesions.
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IgA deficiency. No blood or plasma transfusions! #1 congenital immunodeficiency. Diarrhea usually G. lamblia, sinopulmonary infection with S. pneumo, H. flu, or S. aureus. Assoc with allergies/autoimmune dx. May be d/t isotype switching defect.
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7 month M recurrent URIs, skin infections, and asymetric arthritis of the kness. No tonsillar tissue on exam.
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X-linked hypogammaglobulinemia. Selective B-cell defect. Recurrent bacterial infections. a.k.a. Bruton's disease. Tyrosine kinase receptor defect, impaired maturation of antibodies. Labs = panhypoglobulinemia: very low IgG; IgA and IgM not detectable.
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15yo M with thick yellow discharge that prevents eye-opening in the morning.
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Conjunctivitis. Rx topical AB drops. Usually viral = adenovirus. Self-limiting. Secondary staph/strep may result.
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8yo F with rash, diffuse joint pain, fever, and sore throat two weeks ago.
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Acute rheumatic fever. Erythema marginatum = blanching ring-shaped over trunk and extremities. Elevated ASO titer, incr ESR, incr C-reactive protein. Blood culture negative. Endo/myo/pericarditis. Rx aspirin/corticosteroids, pcn/erythromycin.
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35yo F with pain in upper teeth and face, nasal congestion and discharge.
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sinusitis. boggy nasal mucosa. Common pathogens = S. pneumo, other streptococci, H. flu, Moraxella. Rx amoxicillin or TMP-SMX, decongestants.
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48yo missionary returns from West Africa with lethargy, nuchal rigidity, HA, drowsiness.
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African trypanosomiasis. Tsetse fly. Painless lymphadenopathy in posterior neck & supraclavicular = Winterbottom's sign. Does not respond to antibiotic rx. Chancre with induration at bite site. AKA African sleeping sickness. Rx suramin / pentamidine.
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45yo M Peace Corps in Mexico with spiking fever, RUQ pain, and bloody diarrhea with mucus. Tender hepatomegaly on exam.
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Amebic liver disease. Entamoeba histolytica. Cavitating liver lesion with chocolate-colored pus that is sterile, ameba obtained from periphery of lesion. Rx includes metronidazole and abscess drainage.
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30yo sheep farmer with dyspnea, nonproductive cough, and black skin lesions.
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Anthrax. CXR c mediastinal widening = hemorrhagic mediastinits. Vesicular papules covered by "black eschar". Bacillus anthracis. Rx IV penicillin G. Isolation precautions. Cell-free anthrax vaccine for high risk groups.
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38yo M on chemotherapy with pleuritic chest pain, fever, and productive cough.
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Aspergillosis. Multiple nodular infiltrates. Branched hyphae c silver stain, vascular invasion --> thrombi. Rx Amphotericin B c flucytosine. Lobectomy for fungus ball. Invasive dx: AIDS, neutropenia, chronic granulomatous dx, steroid rx, transplant pts.
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25yo M c sudden onset double vision, dry mouth, weakness, dysarthria, and dysphagia. Ate some home-canned peaches the night before.
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Botulism. Flaccid paralysis. Rx antitoxin, resp. support. Botox cleaves synaptic docking/fusion machinery. Disease d/t ingestion of toxin produced by C. botulinum. Often seen in infants after honey.
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28yo M with hip pain, undulating fever for two months, and pain in testicle. Drinks unpasteurized milk.
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Brucellosis. Blood culture demonstrates B. abortus, transmitted from milk or direct contact with animal tissues. Rx combination of doxycycline/SMX-TMP plus rifampin/streptomycin.
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49yo obese, diabetic F with pruritus underneath her breasts.
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candidiasis. Denuded, beefy red areas with whitish curd-like material. Budding cells with short hyphae on KOH prep. Rx clotrimazole, keep area dry.
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24yo F with fever and swelling over eye after trip to Brazil.
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Chagas dx. Eye swollen shut = Romana's sign. Encapsulated, nodular area at bite site = Chagoma. Ipsilateral retroauricular & cervical nodes. Trypanosoma cruzi, reduviid bug injects feces. Complications = dilated cardiomyopathy, megaesophagus/colon.
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30yo M with profuse watery diarrhea, vomiting, and abdominal pain following trip to India.
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Cholera. Vibrio cholerae. Severe dehydration, rice-water stools gram - rods c darting motility, O1 antigen, decreased serum chloride with increased serum sodium. Heat-labile exotoxin, stimulates Gs via ADP ribosylation incr cAMP --> secretory diarrhea.
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19yo Arizona migrant worker with cough, pleuritic CP, fever and tender nodules over the both shins.
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Coccidioidomycosis. Erythematous skin rash, erythema nodosum, positive skin test with coccidioidin, dimorhphic fungi, eosinophilia, caseating granulomas. Rx amphotericin B. Endemic in southwestern US. Inhalation of spores.
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30yo M with AIDS presents with profuse, nonbloody diarrhea.
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Cryptosporidium parvum. Dehydration. Acid-fast stain --> oocyts in fresh stool. Rx is supportive only. Self-limiting in immunocompetent pts.
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13yo F s/p BMT on immunosuppresion now with fever, dyspnea, dry cough.
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CMV pneumonitis. Insterstitial pneumonitis, intranuclear inclusions with surrounding halo (owl's eye). Rx ganciclovi ). #1 pneumonia and death in BMT patients. Common in AIDS. Enveloped dsDNA herpesvirus.
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5yo M with fever, cervical lymphadenopathy, and grey membrane on tonsils.
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Diptheria. Cornybacterium diphtheriae growth on Loffler's blood agar. Heat-labile exotoxin --> myocarditis and neuritis (blocks EF-2 via ADP ribosylation --> decr ribosomal fnctn & protein synth. Rx: PCN or erythromycin, antitoxin.
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56yo veterinarian with sudden high fever, jaundice, and RUQ pain.
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Echinococcosis. Hepatomegaly, + immunoblot test : echinococcal antigens, large septated liver cysts. +/- lungs/kidneys/bone/brain. Scoleces c inner germinal & outer laminated layer, fibrotic rxn. Rx: surgical cyst removal, albendazole.
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36yo woman with AIDS and pneumonia develops spiking fever, chills, and delirium.
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Endotoxic shock/gram neg. sepsis. E. coli on urine & blood culture. CXR with fluffy infiltrates (ARDS). Sequelae: ATN, DIC, multiorgan failure. Rx: fluid, IV ABs, manage ARDS c O2 and PEEP. Usually d/t gram negative endotoxins &gram positive exotoxins.
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28yo Guatamalan refugee with severe headache, fever, and rash on trunk and extremities; palms and soles spared. Spent time in refugee camp.
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Epidemic typhus. Rickettsia prowazekii. Cerebral edema/myocarditis/pneumonia, peripheral spreading rash. + Weil-Felix rxn. Path: Zencker's degeneration of striated musc. Rx: tetracycline, chloramphenicol. Intracellular. Lice vector. war/famine/crowding.
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21 yo F with low-grade fever, pain and swelling over left knee, and dysuria.
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gonnococcal arthritis. Intracellular diplococci bean-shaped. Migratory polyarthralgias. Incr WBCs c urethral smear & synovial fluid. Rx: IV ceftriaxone. Rapidly destroys cartilage. Associated with skin rash over affected joint, complement deficiencies.
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19yo M with burning urination and greenish-yellow purulent discharge.
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gonorrhea. Intracellular gram negative diplococci, confirmed c Thayer-Martin medium culture. Rx: Ceftriaxone + doxycycline/erythromycin for Chlamydia coverage. Gonorrhea can involve throat, anus, rectum, epididymis, cervix, fallopian, prostate, joints.
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25yo M with painful skin rash in the perianal area.
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Herpes simplex 2. Vesicular in clusters with clear fluid over erythematous base. Giant cells on Pap-stained scraping. Rx: acyclovir. dsDNA virus. Transmitted to fetus through birth canal.
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27yo F with two months fever, mouth ulcers, fatigue, and weight loss. Started new job on farm in Ohio.
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histoplasmosis. Histoplasma capsulatum.Rx: itraconazole or amphotericin B. Intracellular budding fungus in reticuloendothelial cells. Hilar adenopathy. Associated with bird or bat feces. Transmitted by inhalation of mold spores.
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37yo M black male from the Caribbean with swollen glands in armpits and groin, feeling of heavyness in abdomen.
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Human T-cell leukemia virus type 1 (HTLV-1). Lymphadenopathy & splenomegaly. Skin biopsy --> leukemic CD4+. Type C is assoc. c adult T-cell leukemia/lymphoma --> high incidence blacks in Carribean/SE US, Subsaharan Africa/Japan.
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20yo M with sore throat, lymphadenopathy, and malaise.
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IM (EBV). Lymphocytosis c atypical lymphs. Incr ALT/AST/bili. Positive heterophil Ab test (Monospot / Paul-Bunnell test). IgM antibodies to viral capsid = monospot positive.
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40yo M smoker with high fever, nonproductive cough, pleuritic CP, and coworkers with similar symptoms.
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Legionella pneumonia. Gram stain shows no organisms. Direct immunofluorescence confirms indirect fluorescent antibody titer. CXR: ill-defined nodules. Rx: erythromycin. Outbreaks d/t drinking water, humidifiers.
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30yo Pakistani immigrant with history of red papule on arm following insect bite; now with chronic fever, skin darkening, and massive splenomegaly.
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Leishmaniasis / "kala azar". Leshmania donovani zoonosis. Transmitted by Phlebotomussandfly. Labs = anemia, leukopenia, thrombocytopenia. Amastigotesin buffy layer. Rx: pentavalent antimony = Na stibogluconate; amph. B, or pentamidine.
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26yo M from India with hypopigmented anesthetic skin patch on face and swelling in elbow in area of ulner nerve.
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Leprosy: Mycobacterium leprae. Acid-fast bacillus. Thermolabile, divides slowly --> long course. Tuberculoid = skin with limited nerve /involvement (ulner/peroneal). Lepromatous = diffuse skin involvement/eyes/nerves/disfigurement (leonine facies).
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12yo M with fatigue, joint pain, and rash.
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Lyme. Borrelia burgdorferii, spirochete. IgM ELISA, confirm c WB. Rx: doxy or amox. 3 stages; 1= erythema chronicum migrans + constitutional si/sx. 2= cardiac & neuro. 3= persistent migratory arthritis/synovitis/acrodermatitis chronicum atrophicans.
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25yo with tender masses and painful groin ulcers after unprotected sex.
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Lymphogranuloma venerum. Inguinal adenitis, buboes. + complement fixation and IF tests. Ulcerated nodule --> secondary = inguinal bubo (enlarged node +/- fistula/balanitis/phimosis/rectal involvement. Rx: doxycycline. An STD d/t C. trachomatis (L1/2/3).
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30yo missionary with high fever, chills, and severe HA after returning from Africa 1 wk ago.
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Malaria. peripheral smear = plasmodia in erythrocytes. Rx: chloroquine, quinine for cerebral malaria, tetracycline for resistant areas. Anophelesmosquito. Plasmodium falciparum may be lethal --> cerebral malaria.
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12yo F with fever, severe HA, and stiff neck who fainted at school.
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Meningococcemia. +/- petechial rash. Kernig's / Brudzinski's. CSF = incr prot, low gluc. Hypoglycemia, hypo-Na, hyper-K = Waterhouse-Friedrichsen's = adrenal necrosis --> death. Rx: steroids, IV fluid, DA, PCN-G. Prophylactic rifampin for contacts.
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24yo F in hospital for DKA develops periorbital swelling and purulent postnasal discharge that fails to respond to ABs. PE reveals black ulceration of nasal mucosa.
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Mucormycosis. Irregular nonseptate hyphae branching at wide angles. Mucor and Rhizopus molds. Conjunctival swelling = chemosis, black ulceration of nasal mucosa, CNIII palsy, necrotic destruction. !Suspect if AB-resistant sinusitis in DM/lymph/leukemia!
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20yo M college student with productive cough, malaise, and fever. Cough started out nonproductive.
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Mycoplasma pneumonia. CBC: normal leukocyte count. Elevated cold agglutinin titer >1:128. CXR: patchy infiltrates appear worse than clinical picture. Rx: erythromycin. #1 atypical pneumonia. Rapid spread in close quarters.
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45yo M undergoing chemotherapy for Hodgkin's now with SOB/cyanosis; has had greenish sputum for 3 months.
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Nocardiosis. Gram + filamentous, partially acid-fast bacteria. Nocardia asteroides. Chronic infection: DM/leukemia/lymphoma/IC'd pts. Usually lungs, +/- brain/SC tissue. Rx: SMX-TMP 6mo.
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56yo F with visual acuity change, generalized itching after showering, and recent travel to tropics.
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River blindness. Hypopigmentation, nodules, keratitis, chorioretinal lesions.Diethylcarbamazapine --> pruritus, rash, fever, conjuctivitis = Massotti reaction. Rx: ivermectin. Blackfly --> Onchocerca volvulus. Larvae in SC tx and lymphatics.
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28yo diabetic with immobility of knee, swelling, tenderness, and elevated ESR.
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Osteomyelitis. Periosteal thickening. New bone = involucrum traps necrotic bone = sequestrum. Rx IV ABs, surg. #1 =Staph > strep > enterobacteria. SC = E. coli > Salmonella. DM/puncture = Pseudomonas. IC'd = Sporothrix.Human bite = anaerobes.
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18 month F with irritability and ear discharge. Recurrent URIs.
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Otitis media. E. coli,staph, Klebsiella (neonates); S. pneumo, H. flu, Morexella, group A strep (kids). Rx amoxicillin-clavulanate. Complications = ingrowth of epithelium of middle ear = cholesteatoma. Hearing loss, mastoiditis, CNS abscess.
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25yo M bitten by a cat with shiny, edematous tender hand draining purulent fluid.
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Pasturella multicoda. Gram neg rod with bipolar staining. Catalase and oxidase positive. Rx: Incision and drainage + amoxicillin/clavulanate, tetracycline, or penicillin. Can progress to osteomyelitis.
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14yo M bitten by younger sister with shiny, edematous, tender hand draining fluid.
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Eikenella corrodens. Rx: PCN + I&D.
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44yo archaeologist returns from dig site in Arizona with high fever, severe myalgia, and painful inguinal swelling.
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Plague. Yersinia pestis. Enlarged inguinal nodes = buboes. No genital lesions. Gram negative bacilli c safety pin appearance in aspirates from buboes. Rx: streptomycin / tetracycline. Rodents and fleas in Southwestern US. Death rapid if untreated.
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11yo M with blood-tinged, mucoid sputum and pleuritic chest pain.
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Pneumococcal pneumonia. Incr fremitus & dullness over afffected lobe. Gram positive diplococci in sputum, alpha-hemolytic colonies. CXR = homogenous opacification of affected lobe +/- pleural effusion. Rx: IV PCN. #1 community acquired pneumonia.
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32yo HIV + M with progressive dyspnea over 3 wks.
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PCP. dry cough, fatigue, hypoxemia out of proportion to clinical findings. Rx: SMX-TMP. Interstitial pneumonia in IC'd pts. Bactrim prophylaxis for HIV pts if CD4 <200. Labs: serum LDH elevated.
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14yo M Russian immigrant with weight loss, fever, night sweats and bloody sputum.
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TB. Primary = lower lobes / subpleural. Secondary = cavity lesions in upper lobes. Rx: RIPE therapy = rifampin, isoniazid, pyrazinamide, ethambucil.
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28yo M with numbness of R arm following bat bite. Refuses to drink water.
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Rabies. Hydrophobia, neuropathy. Long incubation period 3-8wks, prevent occurrence with vaccine. Negri bodies = cytoplasmic inclusions in Ammon's horn. Positive rabies antigen on corneal scraping.
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27yo Peace Corps volunteer in Africa with fever, sweats, abdominal pain. Had an itchy rash after swimming several weeks ago.
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Schistosomiasis. CBC: eosinophilia. Rx: praziquantel. Snail-infested ponds/lakes. Hepatosplenomegaly d/t portal hypertension d/t granulomas = periportal fibrosis.
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36yo M executive with sudden nausea, vomiting, and diarrhea with blood and mucus after business trip to South America.
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Shigellosis. + fecal leukocytes. Shigella on stool culture. Not motile. Outbreaks c overcrowding, fecal-oral. Can be complicated by Reiter's syndrome = arthritis, conjunctivitis, urethritis (HLA-B27 individuals). Rx: ampicillin or SMX-TMP.
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37yo with ulcerated nodule on hand after trauma while doing yardwork.
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Sporotrichosis. Sporothrix schenckii. Nonpainful, soft, ulcerated nodule at inoculation site = sporotrichotic chancre. Rx: itraconazole. (Sporothrix is a dimorphic fungus = cigar shaped budding cells). May cause bone/joint infection.
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9yo M with odynophagia and erythematous tonsils with white exudate.
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Strep pharyngitis. Rx: oral penicillin V. Streptococcus pyogenes. Complications include glomerulonephritis and rheumatic fever.
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38yo diplomat in Nigeria with diarrhea, fever, dry cough, and dyspnea. Frequently walks barefoot through his neighborhood.
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Strongyloidiasis. Eosinophilia with motile rhabditiform larvae. Rx: thiabendazole or ivermectin. Results from poor hygeine in tropics. CXR: bilateral transient migratory infiltrates.
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54yo F with spiking fever, loss of appetite, and RUQ pain who underwent emergency cholecystectomy 10d ago.
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Subdiaphragmatic abscess. Rx: percutaneous drainage. Findings include pain on percussion, left-shift, fluid collection below diaphragm. Occurs typically >1wk after abdominal surgery.
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18yo M with painless ulcer on penis.
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Syphillis. Dark-field exam of exudate = treponemes. VDRL and FTA-ABS positive. Rx: Benzathine PCN IM, 2.4U single dose. STD d/t Treponema pallidum.
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23yo F with nonpruritic skin rash, hair loss, and copper-colored maculopapular rash on palms and soles.
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Secondary syphilis = generalized tender lymphadenopathy, rash on palms/soles, coalescent papules/plaques in groin = condyloma lata, hair loss = alopecia. Rx: IV benzathine PCN.
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12yo M with dysphagia. Stepped on a nail about a week ago.
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Tetanus. Clostridium tetani. Trismus = jaw m rigid, Risus sardonicus = facial m spasm; dysphagia, neck rigidity, painful facial spasms, opisthotonos. Rx: debride wound, tetanus immune globulin IM or intrathecally, diazepam; tetanus toxoid; IV PCN.
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40yo HIV + M with severe HA. Has 2 cats at home.
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Toxoplasmosis. Toxoplasma gondii. Host = cats. Rx: pyrimethamine or sulfadiazine. PE reveals generalized lymphadenopathy, papilledema. CT/MRI-head reveals mass lesions with ring or nodular enhancement. Compl include seizure, brain abscess.
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50yo M with generalized myalgia and low-grade fever. Had severe abdominal pain and diarrhea several weeks ago after eating at a pigroast.
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Trichinosis. Labs: elevated CPK, LDH, and AST. Normal ESR. Eosinophilia. Raw/undercooked pork. Trichinella spiralis. Affects facial, neck, lower back, and diaphragm. Biopsy of SCM reveals organism.
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20yo M with ulcer on wrist, lymphadenopthy in ispilateral axilla with suppuration. Recently trapped and disposed of rabbit on his property.
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Tularemia. Francisella tularensis. Rabbits, squirrels, rodents, ticks. E levated ESR. Lymph nodes with suppuration + necrosis. Direct fluorescentantibody staining. May be tonsillar, oculoglandular, pneumonitic, typhoidal. Rx: streptomycin + tetracycline.
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27yo M with increasing fever, constipation, and faint erythematous macules over the trunk. Visited Southeast Asia three weeks ago.
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Typhoid fever. Salmonella typhi. Rx: ciprofloxacin. Infection of Peyer's patches c subsequent mucosal necrosis. Fever c stepladder pattern. Macules = "Rose spots" Infection from contaminated food or water. Typhoid vaccine available.
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5yo M with pruritic rash on scalp, face and trunk.
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Varicella zoster. Lesions appear in crops q3-5d. Macules, papules, vesicles, pustules, and scabs all present at same time. Leukopenia. Tzank smear = inclusion bodies (Lipschutz bodies) + MNG cells. DNA herpesvirus.
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45yo HIV+ M with painful, burning skin rash on left side of chest.
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Zoster (shingles). Vesicular rash on erythematous base. Dermatomal distribution. Exquisitely tender. Acantholytic cells on Tzanck smear from base of vesicles. Cowdry A = intranuclear eosinophilic inclusions surrounded by clear halo. Rx: acyclovir.
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24yo South American male develops high fever. He develops yellow eyes, and coffee-ground emesis four days later.
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Yellow fever. Flavivirus transmitted by Aedes mosquito. Affects liver and kidneys: liver midzonal lobular necrosis, severe renal tubular damage. Rx: symptomatic only. Preventable by vaccine. 5-10% mortality, most cases mild.
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50yo M with sudden fever, chills, neck stiffness.
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Bacterial meningitis. S. pneumoniae = most common adult. Photophobia, obtundation. Tap = high pressure, cloudy, high protein, very low glucose, high cells mostly WBCs.
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33yo HIV+ M with persistent HA.
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Cryptococcal meningitis. Encapsulated spherical fungi on India ink prep. CT/MRI-brain multiple ring-enhancing lesions. Rx: amphotericin B + 5-flucytosine. Acquired from pigeon droppings, usually seenin IC'd pts.
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30yo HIV+ M with rapidly progressive visual loss.
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CMV retinitis. Cotton-wool exudates, necrotizing retinitis, perivascular hemorrhages. Rx: ganciclovir; foscarnet. Occurs in 20% of AIDS pts. Blindness in HIV = toxoplasmosis, PML, and CMV.
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45yo hog farmer with visual loss, severe HA, and projectile vomiting.
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Neurocysticercosis. Taenia solium. Papilledema, free-floating cysts in vitreous body of right eye. Ingestion of ova is fecal-oral. CT/MRI-brain: intracranial cysts or calcifications. Eosinophilia.
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54yo man with ataxia, MS changes, deformed ankles, and shooting pain in extremities.
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Tertiary syphillis. Gummas = subcutaneous nodules. Dorsal column --> reduced position/vibration sense. Charcot's neuropathic arthropathy. Broad-based gait. Romberg's sign. Light reflex lost with retained accomadation = Argyll Robertson. "Tree-bark" aorta.
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25yo F with dysuria, frequency, and hematuria after her honeymoon.
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Acute cystitis. E. coli > Proteus, Klebsiella, Staph. saprophyticus, and Enterococcus. Hemorrhagic cystitis may also result from adenovirusinfection.
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28yo F in 27th week of pregnancy with R flank pain, fever, and dysuria.
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Acute pyelonephritis. UA: proteinuria, WBC casts, >100,000 cfu E. coli. Rx by sensitivity, ampicillin empirically. E. coli, Klebsiella, Proteus, and Enterobacter.
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19yo M with painful urination and yellow-green urethral discharge. No bacteria seen on Gram stain.
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Nongonnococcal urethritis. Rx: doxycycline. Most common = C. trachomatis, also Ureaplasma urealyticum. Frequentl coinfection c gonnococcal urethritis. Direct immunofluorescence using monoclonal Ab to Chlamydia. No growth on culture.
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15yo M with painful bilateral parotid swelling and left-sided scrotal pain.
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Orchitis. Mumps, E.coli, enterobacteria, chlamydia, gonnorhea, mycobacterium tuberculosis. May cause sterility if bilateral. Rx: scrotal support, ice packs, steroids. CBC: lymphocytosis, hyperamylasemia.
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25yo F with burning on urination.
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UTI. E. coli, staph saprophyticus = #1 and 2 causes. Others include proteus, klebsiella, enterobacter, serratia, psuedomonas, enterococcus, chlamydia, neisseria. Risk = females, sex, pregnancy, obstruction, bladder dysfunction, reflux, catheters.
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34yo M with multiple myeloma develops reticular skin infarction, necrosis, and ulceration.
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Cryoglobulinaemia. Associated with paraproteinemias, RA, SLE, mononucleosis, lymphoma, PBC, and HCV. Small vessel vasculitis that may involve kidneys = renal failure. Rx: plasmapheresis.
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54yo F with RA develops Bence Jones proteinuria.
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Monoclonal gammopathy of uncertain significance (MGUS). Monoclonal paraprotein without B-cell tumor. Assoc c hepatitis, leptospirosis, autoimmune dx. Follow closely 10-20% develop myeloma. Rx: None necessary. Close f/u.
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78yo M with fever, anemia, fatigue, petechiae and recent lacunar stroke.
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Waldenstrom's macroglobulinemia. Old men 2:1. Normochromic normocytic anemia. Rouleaux RBCs. ESR elevated. Serum M protein, cryoglobulin, and cold-reacting Abs. Hyperviscosity --> stroke, MI, Raynaud's, pyoderma gangrenosum.
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55yo M with anemia, leukopenia, thrombocytopenia and bone pain.
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Multiple myeloma. Infections (70%), renal failure (50%), bone pain (100% with progression), bleeding (10%). Very high ESR, rouleaux RBCs. Diagnosis = 2 of following: Bence Jones, bone marrow plasma cells, punched-out bone lesions.
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19yo M with recurrent DVTs for one year.
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Antithrombin III deficiency. Diagnosis = antithrombin level. Rx: coumadin. AT-III activity enhanced by binding heparin (don't use heparin to treat AT-III deficiency). Inherited disorder, screen family. Onset in late teens typical.
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24yo M with recurrent DVTs. Family history of DVTs affecting mother and sister.
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Factor V Leiden. #1 thrombophilia. 20-40% of pts c DVTs esp. young ages. Auto dom: homoz's with 80x risk, hetero 7x risk. Incr risk in pregnancy & contraceptive use. Mutation eliminates protein C cut site. Rx: coumadin for homos, prophy for hetero's.
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23yo M bitten by snake now with purpuric skin lesions.
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DIC. Causes include meningococcal, snakebite, staph septicemia, obstetric, malignancy (bronchus, pancreas, ovary, prostate, leukemias), shock, massive transfusion, vasculitis (HUS/TTP), bypass, cavernous hemangiomas.
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16yo M with massive hematomas and no history of trauma.
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Differential includes: Christmas dx, von Willebrand's, hemophilia, or uncontrolled anticoagulation.
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15yo M with acute hot, red, swollen knee and easy bruising.
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Hemophilia. Prolonged aPTT, normal PT. Rx: factor VIII replacement. X-linked recessive.
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13yo M with recurrent bleeding episodes and normal factor VIII levels and activity assay.
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Christmas disease. Factor IX deficiency. Complications of both include: chronic degenerative joint dx, compression neuropathy, renal pelvic / ureteral obstruction, intestinal obstruction.
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53yo homeless man with bleeding gums, purpura, and perifollicular bleeding.
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Scurvy = vitamin C deficiency.
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6yo F with generalized skin rash following mild URI. Rash became purpuric after one day.
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HSP. Drugs, food, insect bites, infections. Purpura +/- glomerulonephritis. Immune complex deposition. Children > adults. Glomerulonephritis in 33%.
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14yo with recurrent epistaxis and multiple small red lesions on lips, mouth, tongue. Mother and uncle have similar condition.
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Hereditary hemorrhagic telangiectasias = Osler-Weber-Rendu. Autosomal dominant. Mucosal bleeding. Association with pulmonary AV fistula.
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9yo F with recurrent URIs, diarrhea, and failure to thrive.`
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CF. High Cl sweat test.CXR: brochiectasis. Pseudomonasand staph infections of the lung. Mucous plugging, small bowel obstruction = meconium ileus. Rx: pulmozyme (DNAse breaks up airway). Azithromycin. Inhaled tobramycin (Tobi). Male sterility.
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23yo M with chronic productive cough and wife with difficulty becoming pregnant. Apical impulse not present on L side.
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Kartagener's syndrome. Sperm immotility, bronchiectasis. Dynein defect leads to immotile cilia. Autosomal recessive. Dextrocardia.
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23yo M goes to family doctor for evaluation of sterility. Found to have height greater than arm span, crown-pubis length greater than pubis-floor.
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Klinefelter's. 47XXY. Male hypogonadism. High incidence of breast CA, COPD, DM, mild mental retardation. PE: small testes, gynecomastia, "eunuchoid" body proportions. Increased gonadotropin with reduced testosterone.
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26yo M with flat nose, and single palmar crease. Had silver spots on iris at birth.
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Down's. Epicanthal folds, Brushfield spots, Simian crease. Double bubble on KUB: dilated stomach proximal duodenum d/t duodenal atresia. Hypoplastic phalanges in 5th digits (acromicria). Usually nondisjunction; Robertsonian translocation or mosaicism.
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7yo boy with diminished visual acuity and long arms, legs, and fingers.
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Marfan's syndrome. Arm span > height, arachnodactyly, ectopia lentis, severe myopia, high-arched palate, flat feet = pes planus, aortic insufficiency, pectus excavatum. Rx: beta-blockers, endocarditis prophy. Auto-dom. fibrillin = elastin scaffold.
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17yo F with amenorrhea, lack of breast development, and harsh systolic murmur.
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Turner's. Short stature, webbed neck, shield-like chest with wide-spaced nipples. High serum FSH/LH; no Barr bodies on buccal smear. Get US pelvis --> streak ovaries. Karyotype 45, XO; sometimes mosaicism --> skeletal, CV, horshoe kidney.
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5yo Asian F with sudden eye pain and loss of vision after watching a film. Reports seeing halos around lights at night.
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Acute glaucoma (angle closure). Hazy cornea, elevated intraocular pressure. Rock-hard eye. Rx: analgesics, IV acetazolamide, topical beta-blocker, steroids, pilocarpine, laser iridotomy. Precip'd by mydriatics and switch from dark to well lit areas.
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49yo M with progressive weakness, difficulty speaking, and fasciculations.
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ALS. Bilateral hand wasting, DTRs absent in upper limbs, muscle weakness, + Babinski sign (upgoing great toe) = upper motor neuron sign. Involves both upper and lower motor neurons. CSF normal. CT/MRI-brain normal.
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40yo M, now unresponsive, found in bathroom at work projectile vomiting. Said he was "seeing double".
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Cerebral aneurysm. Papilledema, CNIII palsy. Congenital Berry aneurysms associated with polycystic kidney disease, AV malformation. Cause subarachnoid hemmorhage. ACOMM > PCOMM > POST CEREBRAL.
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14yo M with short stature, history of polyuria, and peripheral vision loss.
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Craniopharyngioma. #1 supratentorial tumor in kids. Derived from Rathke's pouch remnants. Common cause of growth retardation, diabetes insipidus, bitemporal hemianopia, and headache d/t obstructive hydrocephalus. Bimodal with peak in fifth decade.
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62yo M with rapidly progressing decline in cognitive function, somnolence, and clonus on exam.
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Creutzfeld-Jakob. Subacute spongiform encephalopathy. Risk = dura mater, corneal transplants, cadaveric growth hormone, neurosurgical contamination. Lithium OD may mimic presentation.
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19yo F horseback rider was thrown off horse. Lost consciousness then recovered. Now with HA, confusion, and weakness of left side with projectile vomiting.
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Epidural hematoma. "Lucid interval" is classic. Signs = bradycardia, papilledema, mydriasis and CNIII palsy on ipsilateral,extensor plantar response and weakness on contralateral. CT --> lens-shaped, convex extra-axial fluid collection btwn dura & skull.
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19yo M with wide-based gait, clubfoot, and lateral curvature of spine.
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Friedreich's ataxia. #1 hereditary ataxia. Auto-dom, chromosome 9. Degeneration of doral root ganglia --> prorioceptive loss, areflexia, ataxia, Babinski's. Also causes visual loss, hypertrophic cardiomyopathy.
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60yo M with HA worse in morning, nausea, and vomiting for six weeks.
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Glioblastoma multiforme. CT = irregular enhancing left-sided mass with necrotic center; mass effect and surrounding edema.
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38yo M with symmetric muscle weakness started in feet, now involving legs and shoulders. Had diarrhea and fever.
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Guillain-Barre. Symmetrical proximalweakness / flaccidity. Increased CSF protein concentration without cellular increase. VDRL negative. Decreased nerve conduction velocity. Preceeded by GI/respiratory/EBV/Campylobacter/CMV +/- respiratory paralysis.
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65yo M with sudden severe HA and hemiplegia. Now incontinent.
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Hypertensive stroke.
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59yo F with retro-orbital HA and diplopia. Diagnosed with lung cancer.
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Metastatic dx. Intracranial mets from lung, breast, GI, GU, CA, and melanoma.
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25yo with weakness, droopy eyelids, double vision, and dysphonia.
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Myastenia gravis. Autoimmune c Abs to acetylcholine receptor subunits. Thymoma is present in 20% of cases.
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46yo M with HAs in the morning, seizures, and CT showing nodular calcifications in a frontal lobe mass.
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Oligodendroglioma. Usually low grade, but may be anaplastic. More sensitive to chemo than astrocytomas. Calcification in 90% of cases.
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30yo M with anesthesia and weakness in both arms, occipital HAs, and stiff gait.
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Syringomyelia. MR/CT --> cystic dilatation within central cervical cord. Hydromelia is lined by ependymal tissue, syringomyelia is not.
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18yo M with wide-based gait and headaches. Father died of renal cell carcinoma at young age.
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von Hippel-Lindau. Auto-dom, renal cell CA + renal, hepatic, pancreatic cysts + cerebellar ataxia.
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49yo alcoholic with confusion, stupor, and nystagmus following 5% dextrose infusion.
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Wernicke's encephalopathy. Due to thiamine deficiency.
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22yo F with abnormal Pap smear and no history of irregular menstrual, postcoital bleeding, or vaginal discharge.
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Cervical carcinoma in situ.
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29yo Vietnames F with nausea, vaginal bleeding, dyspnea, and hemoptysis.
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Choriocarcinoma. Can develop during normal pregnancy, s/p hydatidiform mole, or previous spontaneous abortion. Elevated hCG.
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45yo F with gross difference in size of her breasts with sensation of fullness but no pain. Exam reveals large, firm mass.
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Cystosarcoma phyllodes. Less common benign tumor of breast. Mass tends to be mobile and is well circumscribed. Path = cystic spaces on cut section, producing recesses and longitudinal openings with 'leaflike' (phyllodes) appearance.
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25yo W with amenorrhea for 6 weeks and development of pelvic pain for 1 day.
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Ectopic pregnancy. Risk factors = previous tubal surgery, tubal ligation, endometriosis, previous ectopic pregnancy, ovulation induction, pelvic inflammatory disease. Test of choice = hCG and ultrasound (can get transvaginal US if needed).
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60yo F with obesity presents with intermittent vaginal bleeding for three months. Has never had children.
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Endometrial CA. Estrogen-dependent cancer. Rx: hysterectomy, radiation. Important to include in differential of postmenopausal bleeding.
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27yo with inability to conceive, painful intercourse, and painful menses.
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Endometriosis = extrauterine endometrial tissue. Can be located in various locations with unique symptoms , most frequently bilateral ovaries = chocolate cysts.
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27yo F marathon runner with painful lump breast. Mammography reveals irregular mass with focal areas of calcification.
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Fat necrosis. Indurated lesion with retraction of overylying skin. Unilateral localized process associated with trauma, breast biopsy, and radiation. Easy to confuse with CA… pain is the key distinguishing feature.
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25yo F with right breast lump that is small, encapsulated, and freely moveable.
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Fibroadenoma. #1 benign breast tumor in young women; sometimes enlarges during pregnancy or normal menstrual cycles. Mammogram = "popcorn calcifications".
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20yo F with chronic left lower quadrant pain and left adnexal mass on exam.
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Follicular ovarian cyst. #1 cause of ovarian enlargement. Test = US to look for cyst. Rx: Follow-up ultrasound (many disappear spontaneously); laparoscopic removal if persistent.
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52yo nulliparous F with painles lump in breast. PE reveals fixed, hard, nontender mass with retraction of overlying skin and palpable ispilateral nodes.
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Infiltrating ductal CA = #1 breast cancer. Risk = family hx, estrogen "exposure", atypical hyperplasia, previous breast cancer. Fibrosis with induration = desmoplastic reaction. Rx = surgery, tamoxifen if E receptor positive.
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59yo F with pain and swelling in breast with erythematous overlying skin with peau d'orange appearance.
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Inflammatory carcinoma of breast. Highly malignant with early and widespread metastases.
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39yo F with heavy and frequent periods, occasionally painful.
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Leiomyoma. #1 tumor of uterus, most common tumor in women. Estrogen-dependent. US reveals multiple heterogenous masses, 95% intramural myometrium location, round, firm, well circumscribed.
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60yo F with foul-smelling, blood-tinged, purulent vaginal discharge. Tumor projecting from cervical os on speculum exam.
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Leiomyosarcoma. CT = large complex mass in uterus. Biopsy = spindle-shaped cells with many mitotic cells. Rx: adriamycin, progestins, combination therapy. Aggressive malignant tumor of the myometrium, can arise from leiomyoma or de novo.
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56yo F with history of breast CA with pelvic mass identified on routine physical exam.
|
Ovarian carcinoma. Serous type most common, often bilateral and advanced at diagnosis. Elevated CA-125, psammoma bodies.
|
|
68yo F with itchy, painless scaling and oozing of erythematous nipple.
|
Paget's carcinoma. Characteristically a scally skin lesion of areola and nipple arising from ductal adenocarcinoma.
|
|
35yo F with bloody nipple discharge originating from one of the duct openings.
|
Papilloma of the breast. Benign proliferation of ductal epithelial tissue. #1 cause of serous / bloody nipple discharge.
|
|
88yo M with purpura over extensor aspect of both hands. CBC reveals not abnormality.
|
Senile purpura. Benign disease of elderly, characteristically extensor hand surfaces, forearms, and neck. Defect in collagen support of dermal cappillaries. No treatment available. Cosmetic consequence only.
|
|
18yo M with small purple skin lesions following URI two weeks ago.
|
ITP. Abrupt onset. Viral illnesses, drugs = thiazides, gold, carbamazepine, phenothiazines, quinine, rifampicin, valproate, sulphonamides, penicillins. Drug binds pltlt or drug binds plasma protein, forms immune complex, binds pltlt. Rx: steroids.
|
|
Causes of purpura.
|
Senile, Osler-Weber-Rendu (hereditary haemorrhagic telangiectasia), giant cavernous hemangioma (can cause DIC), Ehler's-Danlos, Marfan's, HSP, scurvy, Cushing's, steroid use, uremia, liver dx.
|
|
64yo M with testicular swelling.
|
Lymphoma of testis. #1 testicular neoplasm in elderly.
|
|
29yo M with painless lymph node in the axilla, normochromic, normocytic anemia, and elevated ESR. Next test?
|
Node biopsy. Hodgkin's --> Reed-Sternberg. Non-Hodgkins' --> spectrum small lymphocytic (low-grade) to large cell centroblastic (high grade). A2 staging; I=nodes 1 region II=2 regions, same side III=nodes both sides hemidiaphragm, IV=diffuse.
|
|
45yo F with anemia, bone tenderness, and abdominal distension. Smear demonstrates blasts at all stages of maturation. Recent DVT.
|
CML. Philadelphia chromosome 22 bcr-abl translocation 9:22 (95% of cases). Complications = hyperviscosity (rx with leukophoresis).
|
|
60yo F with diffuse lymph node enlargement and smear with increased lymphocytes, smudge cells.
|
CLL. Most common leukemia in US and Europe. Monoclonal transformation of B cells. Diagnosis = persistent lymphocytosis with increased lymphs. Warm antibody hemolytic anemia may result. No rx if asymptomatic.
|
|
Causes of asplenia (anatomic or functional).
|
SLE, sickle cell, celiac, lymphoma, post-surgical. Risk of infection with S. pneumo, H. flu, N. meningitidis, malaria.
|
|
34yo M with facial plethora (redness), conjunctival suffusion, and splenomegaly.
|
Polycythemia. True or d/t excess EPO --> polycystic kidneys, renal CA / cysts, chronic glomerulonephritis, liver disease, hepatocellular CA, overian CA, bronchial CA. Hypoxia, lung disease, congenital heart disease, smoking. Enlarged retinal vessels.
|
|
|
P. vera: Hyperuricemia (rx with allopurinol), thrombotic events (less risk in secondary dx), 20% progress to myelofibrosis. Rx with phlebotomy. High incidence of HTN, itching, hepatomegaly, gout.
|
|
Causes of warm antibody autoimmune hemolytic anemia.
|
Lymphoma, leukemia (CLL), SLE, HIV. Causes spherocytes (also seen in congenital spherocytosis). Rx: prednisolone may induce remission; consider splenectomy.
|
|
Causes of cold antibody autoimmune hemolytic anemia.
|
Infectious mononucleosis, mycoplasma pneumonia, malaria, idiopathic (IgM paraprotein).
|
|
Cigar shaped erythrocytes.
|
Hereditary elliptocytosis. Usually asymptomatic.
|
|
Spherocytes on peripheral smear.
|
Perform osmotic fragility test. Spectrin defect = hereditary spherocytosis.
|
|
2yo with frontal bossing and "hair-on-end" appearance on skull x-ray. Has painful swelling of the fingers.
|
Sickle cell. Salmon-patch retinal hemmorhages. Homozygotes affected, heterozygotes asymptomatic until exposed to low O2 tension. Test with Hb electrophoresis and sickling test.
|
|
25yo black M develops painful joints and severe stomach pain one day into ski trip in the French Alps.
|
Sickle cell trait. Crisis at low O2 tensions.
|
|
Drug induced aplastic anemia.
|
Chloramphenicol, chlorpropamide, chlorpromazine, carbimazole, carbamazepine, gold salts, methotrexate, phenytoin.
|
|
Most common cause of iron deficiency anemia worldwide.
|
Hookworm.
|
|
58yo F with recurrent episodes of thrombophlebitis in the legs and arms.
|
Pancreatic CA. Thrombophlebitis may preceed diagnosis by many months.
|
|
64yo peanut farmer with jaundice, weight loss, and right upper quadrant pain.
|
Hepatocellular CA. Test for alpha-fetoprotein. Ultrasound / CT to evaluate.
|
|
Causes of cirrhosis.
|
Glycogen storage, Fanconi's, alpha-1-antitrypsin (neonatal hepatitis with cirrhosis in childhood), cardiac cirrhosis (late complication of R heart failure), methotrexate, hereditary hemorrhagic telangiectasias, ulcerative colitis and Crohn's.
|
|
17yo M with tremor, athetoid movements, and elevated LFTs.
|
Wilson's disease. Low ceruloplasmin. Kayer-Fleischer ring in cornea. Rx: penicillammine chelation therapy.
|
|
55yo F with pruritus and jaundice that progressed over 3 years.
|
Primary biliary cirrhosis. Anti-mitochondrial Abs. Assoc. c Sjogren's, Raynaud's, thyroid dx, Addison's, RA, fibrosing alveolitis, dermatomyositis, scleroderma. Women 9:1, age 40-60. ERCP reveals normal intra/extrahepatic bile ducts. Gallstones common.
|
|
31yo M with jaundice, pruritus, and RUQ pain. Markedly elevated AP with slight elevation in AST and ALT.
|
Primary sclerosing cholangitis. ERCP shows patchy dilatation and stricturing of biliary tree. High risk of ulcerative colitis. Progresses to hepatic cirrhosis. Risk = ascending cholangitis. HLA B8, DR2, DR3.
|
|
30yo F with hypothyroidism and rheumatoid arthritis develops jaundice.
|
Autoimmune hepatitis. Type I = history or family history of autoimmune disease. Type 2 = anti-liver and kidney microsomal autoantibodies, occurs in younger children. Type 3/4 = soluble liver antigen, type 4 ill-defined similar clinical as type 1.
|
|
31yo F with morbilliform rash and jaundice. Recently seen by a neurolgist for epilepsy.
|
Drug-induced hepatitis. Phenytoin (anti-epilepsy).
|
|
25yo with eosinophilia, chronic cough, and distal small bowel obstruction.
|
Ascaris lumbricoides. Larvae migrate to lung, small bowel obstruction are complications.
|
|
29yo HIV + F with eosinophilia, liver, heart, and renal failure.
|
Strongyloidiasis. Can result in systemic invasion in IC'd pts.
|
|
23yo M former aid worker in Guatemala has resolving bloody diarrhea nd develops stricturing and mucosal damage to colon.
|
Entamoeba histolytica. Don’t confuse with inflammatory bowel disease.
|
|
Diarrhea: viral
|
Rotavirus, Norwalk, Adenovirus.
|
|
Diarrhea: bacterial toxin
|
E. coli (enterotoxigenic), Vibrio cholerae, Staph aureus, Clostridium perfringens, Clostridium difficile, Clostridium botulinum, Bacillus cereus.
|
|
Diarrhea: bacterial invasive
|
E. coli (enteroinvasive), Shigella, Salmonella, Yersinia enterocolitica, Vibrio parahemolyticus, Campylobacter jejuni.
|
|
Diarrhea: parasites
|
Giardia lamblia, Cryptosporidium parvum, Entamoeba histolytica.
|
|
Diarrhea: drugs
|
laxatives, antacids with magnesium
|
|
Diarrhea: food toxins
|
puffer-fish, ciguatoxin, scombroid
|
|
Diarrhea: chronic GI disorders
|
Ischemic colitis, malabsorption, irritable bowel, inflammatory bowel disease
|
|
Diarrhea: secretory
|
Vibrio cholera, campylobacter, E. coli, Salmonella.
|
|
Diarrhea with systemic illness
|
Salmonella typi (enteric fever with diarrhea as late symptom)
|
|
64yo with CAD deficiency develops diarrhea, vomiting, and vague abdominal pain that rapidly progresses to hematochezia and severe abdominal pain.
|
Acute mesenteric ischemia.
|
|
48yo M with recurrent abdominal pain after eating. Also has hypercholesterolemia.
|
Chronic mesenteric ischemia (intestinal angina).
|
|
53yo M with abdominal pain and diarrhea with blood. Plain abdominal film reveals "thumbprinting" pattern in the descending colon and narrowing of the colonic lumen.
|
Colonic ischemia. More common than mesenteric ischemia, typically affects splenic flexure and other watershed areas.
|
|
55yo F previously treated for carcinoma of cervix, now with nausea, vomiting, and rectal bleeding.
|
Radiation colitis. Intestinal ischemia may develop due to endarteritis obliterans. Sometimes pseudo-obstruction. Barium study = thickening of mucosal folds, narrowing of lumen. Symptoms due to rapid transit time and malabsorption.
|
|
38yo F with celiac disease with chronic diarrhea and weight loss. Has been strictly adhering to gluten-free diet.
|
Intestinal lymphoma. Increased risk in celiac disease.
|
|
19yo F with diarrhea and bullous skin eruption.
|
Dermatitis herpetiformis. Gluten senstive enteropathy (celiac disease) + bullous skin eruption. Both may respond to gluten-free diet.
|
|
8yo M with chronic diarrhea, steatorrhea, abdominal distention, and failure to thrive.
|
Celiac disease (Gluten-sensitive enteropathy). Adult presentation more vague with megaloblastic anemia, diarrhea, vague abdominal symptoms. Abs include endomysial, gliadin, and reticulin. IgA endomysial Ab with high sensitivity and specificity.
|
|
Diagnosis of celiac disease?
|
Biopsy! Flattening of vili. Definative diagnosis requires trial of gluten-free diet.
|
|
Causes of malabsorption.
|
Stomach: post-gastrectomy dumping, ZE, pernicious anemia. Hepatic/biliary: bil. obstr. / cholestasis. Pancreas: CF, pancreatitis, CA. Sm. bowel: celiac, crohn's, removal of sm. bowel, fistulae/blind loops, infection, radiation, lymphoma, drugs, whipple's.
|
|
Approach to malabsorption?
|
1. confirm impaired absorption (fecal fat, Schilling test) 2. Identify specific deficiencies (CBC, Fe, iron, folate, B12, PT/PTT, vit D 3. establish cause.
|
|
34yo M with severe recurrent peptic ulcer, diarrhea, and weight loss.
|
Zollinger-Ellison. Gastrin producing tumor associated with MENI (usually pancreatic). Diagnosis = high gastrin level and high basal secretion of acid.
|
|
Upper GI bleeding?
|
GUMBLEEDING = Gastritis, Ulcer, Mallory-Weiss, B, L, Esophagitis, Esophageal varices, angioDysplasia, Infection, N, GERD.
|
|
Common causes of lower GI bleeding?
|
hemorrhoids, anal fissure, inflammatory bowel, diverticulitis, carcinoma, intussusception.
|
|
Test for bacterial overgrowth?
|
glycochocolate breath test, based on deconjugation of radiolabeled bile acid and exhalation of labeled CO2.
|
|
GI utility of US and CT?
|
Liver, pancreas, and biliary tract.
|
|
GI utility of plain film?
|
Demonstrate dilatation (toxic megacolon), obstruction.
|
|
GI utility of angiography?
|
GI bleeding of obscure cause or suspected mesenteric ischemia.
|
|
Unusual causes of lower GI bleeding?
|
AV fistulae, hereditary-hemorrhagic-telangiectasias (Osler-Weber-Rendu), angiodysplasia, vasculitis, amyloidosis. Meckel's, blood disorders (hemophilia, thrombocytopenia), rupture of AAA into bowel.
|
|
Common causes of upper GI bleeding?
|
Duodenal ulcer > stomach erosions / gastritis > GERD > gastric ulcer > Mallory-Weiss > duodenal erosions > esophageal/gastric varices > stomach CA
|
|
Causes of sore tongue?
|
Systemic: folate/B12/Fe deficiency, collagen-vascular dx, diabetes. Local: smoking, fractured tooth/dentures/crowns, candidiasis, dry mouth.
|
|
Teeth and gums
|
Blue line at tooth/gum margin = lead; gingivae swollen and purplish = scurvy; hyperplastic gingivitis = phenytoin, cyclosporin, and calcium antagonists; yellow staining = tetracycline.
|
|
Apthous ulcers?
|
poor dental hygeine, gluten enteropathy, inflammatory bowel dx, Behcet's.
|
|
Enlarged tongue?
|
Acromegaly, myxoedema, amyloidosis, motor neuron disease.
|
|
71yo M smoker with progressive dysphagia.
|
Esophageal CA
|
|
25yo M with progressive dysphagia and no past medical history.
|
Esophageal ring. Occur at or near GE junction. Cause unknown.
|
|
31yo M with HIV and odynophagia.
|
Esophagitis due to candidia, herpes, or CMV.
|
|
H. pylori infection.
|
Association with duodenal ulcer (100%) > gastric (80%) > duodenitis/gastritis. Increased risk of gastric cancer and MALT lymphoma. Test: serology or urease breath test.
|
|
Gastritis causes?
|
Infectious = rotavirus, norwalk, E. coli, H. pylori. Drug/chemicals = aspirin and other NSAIDs, alcohol. Asymptomatic chronic = elderly persons often with H. pylori. Atrophic = autoimmune (positive parietal cell Abs) with pernicious anemia.
|
|
38yo F presents with melena and epigastric pain. Barium study revealed rugal hypertrophy.
|
Menetrier's disease (giant hypertrophic gastritis). Assoc. with protein-losing enteropathy.
|
|
GI disease with finger clubbing?
|
malabsorption, small intestinal disease, and cirrhosis.
|
|
Hormone:
|
Stimulation test and markers:
|
|
ACTH and GH
|
Insulin hypoglycemia test: GH, cortisol, blood glucose
|
|
ACTH and GH
|
Glucacon: GH, blood glucose
|
|
TSH
|
Thyrotropin releasing hormone: TSH, T3, T4, prolactin, GH
|
|
LH, FSH
|
Gonadotropin releasing hormone: FSH, LH, spermatogenesis, ovulation
|
|
GH
|
GHRH: GH
|
|
ACTH
|
CRH: ACTH, cortisol
|
|
ADH
|
Fluid deprivation:
|
|
11yo M with with color blindness, midline facial deformity, and anosmia.
|
Isolated gonadotropin deficiency = Kallman's syndrome. Prepubertal onset, hypogonadal hypogonadism.
|
|
28yo F with resolving meningitis develops polyuria.
|
Central diabetes insipidus. Most frequently associated with craniopharyngioma. Rarely with anterior pituitary disease. Test = water deprivation and measure urine osmolality.
|
|
43yo M with thick skin, broad nose, and prominent supraorbital and nuchal ridges.
|
Acromegaly. Uncommon. May occur in MEN1. Large spade-like hands. Enlargement of the tongue. Hoarse voice. Cardiomegaly, heart failure, and malignancy causes death. Tufting of terminal phalanges on x-ray.
|
|
Elevation of prolactin level due to physiolgic cause?
|
Sleep, stress, nipple stimulation, coitus, pregnancy, suckling.
|
|
Most common cause of Cushing's syndrome?
|
ACTH overproduction by pituitary 60% > ectopic ACTH (15%) > adrenal adenoma (15%) > adrenal carcinoma (10%). Cushing's disease usually pituitary microadenoma (90%) more frequently in women.
|
|
48yo F with develops increasing pigmentation following bilateral adrenalectomy for Cushing's disease.
|
Nelson's syndrome. May follow adrenalectomy if ACTH production continues in excess.
|
|
Diagnosis of Cushing's syndrome.
|
Low dose 48hr dex suppression. Screening with overnight dex suppresion test or 24hr urinary free cortisol. If plasma ACTH is undetectable, usually adrenal tumor. Pituitary-dependent disease suppresses, whereas adrenal tumors and ectopic ACTH does not.
|
|
Ectopic ACTH tumors?
|
Bronchial carcinoma, carcinoid.
|
|
29yo F with SLE and history of DVTs develops increased skin pigmentation and profound hypekalemia.
|
Primary adrenal insufficiency. Antiphospholipid syndrome can destroy adrenal glands.
|
|
31yo M with fatigue, weight loss, GI disturbances, and dark spots on the inside of his cheeks.
|
Addison's disease. Autoimmmune or rarely TB, granulomatous disease, metastases. Other causes of adrenal insufficiency include withdrawal of steroid therapy, Waterhouse-Friderichsen, anticoagulant therapy. Hyponatremia, hyperkalemia, vitiligo.
|
|
Poor growth syndromes?
|
Rare congenital syndromes, nutritional/emotionald deprivation, GH deficiency (fat with immature facies and genitals), hypothyroidism, Cushing's. "Fat and short" likely endocrine. Turner's 45XO, and Noonan's (45XO/XY mosaic).
|
|
34yo F with short stature, large head, prominent forehead and disproportion of body and limbs.
|
Achondroplasia. Autosomal dominant. #1 short stature with abnormal proportions.
|
|
15yo F found on pelvic exam to have bilateral masses in the labia. LH levels is high.
|
Testicular feminization syndrome. XY male with X-linked deficiency of androgen receptors.
|
|
Newborn with ambiguous genitalia, clitoral hypertrophy, and partial fusion of labioscrotal folds.
|
Congenital adrenal hyperplasia. 21-hydroxylase defiency. Excess androgenic cortisol precursors.
|
|
18yo M with small firm testes, gynecomastia, and female distribution of body hair.
|
Klinefelter's. Infertile, may be unusually tall, 47XXY.
|
|
Common causes of amenorrhea?
|
Hyperprolactinemia, weight loss, anorexia nervosa, autoimmune associated ovarian failure (Addison's or other).
|
|
24yo obese F with menstrual irregularity, hirsutism, and acne.
|
Polycystic ovarian syndrome. Stein-Leventhal syndrome = obesity, amenorrhea, and hirsutism. DM2 develops in 40% by age 40. Labs = incr LH, +/- incr T, normal FSH, prolactin and TSH. Pelvic
|
|
61yo M with new onset atrial fibrillation, heart failure, and 20lb weight loss over 12 months.
|
"Masked" hyperthyroidism. Commonly due to toxic multinodular goiter. Lacks typical Grave's features.
|
|
44yo F with diffuse goiter, pretibial myxoedema, and tachycardia.
|
Grave's. IgG antibodies against TSH receptor = thyroid stimulating Abs (TSAb). Exopthalmos, lid lag, periorbital puffiness, increased lacrimation, conjunctival edema, ophthalmoplegia, loss of visual acuity.
|
|
53yo F with hyperlipidemia, puffy face, and coarse hair, and hair loss.
|
Hypothyroidism: Spontaneous atrophic, postsurgical, radioactive I, Hashimoto's (thyroid peroxidase and thyroglobulin Abs in 90%). Dry skin, coarse hair, facial edema, effusion, ascites, cardiac dilatation. Assoc c pernicious anemia and carpal tunnel.
|
|
Most common goitrous hypothyroidism?
|
Hashimoto's. Women >> Men. Older women > younger.
|
|
58yo F from central Africa with large goiter.
|
Endemic goiter. Can be euthyroid. Due to iodine deficiency.
|
|
73yo F with hypothermia and altered mental status and history of hypothyroidism.
|
Myxedema coma. marked by hypothermia, cardiac failure, altered MS, convulsion. Mortality 50%.
|
|
46yo M with painful itchy ear following family vacation to lake. Experiences pain when tragus is pressed during exam.
|
Otitis externa. Symptoms inlcude pain, pruritus, hearing loss, and fullness. Tragus = semicircular cartilage in front of ear canal. Staph and pseudomonas.
|
|
51yo diabetic M with painful itchy ear. Physical exam reveals inflammation and swelling of the pinna.
|
Cellulitis. Differentiate from otitis externa.
|
|
47yo HIV positive M with "boring" ear pain and long-standing ear infection that has not responded well to treatment.
|
Necrotizing external otitis. Occurs in ICd pts. Refer to otolaryngology.
|
|
28yo F with diffusely swollen and tender pinna.
|
Perichondirits. IV antibiotics, serious condition.
|
|
31yo M with circumscribed swellings in the external canal with tenderness on exam.
|
Furunculosis. Rx with topical ABs.
|
|
82yo M with pruritus of the external canal. Whitish exudate with black spots on exam.
|
External mycotica (otomycosis). Aspergillus niger causes black spots over white.
|
|
44yo construction worker with dizziness, tinitus, and conductive hearing loss in the right ear.
|
Cerumen impaction.
|
|
Complications of sinusitis?
|
Osteomyelitis, periorbital infections (pain with eye motion, ptosis, proptosis), cavernous sinus thrombophlebitis (CN III, IV, VI palsies), brain abscess, meningitis.
|
|
Persistent sinusitis?
|
Consider Wegener's granulomatosis, cystic fibrosis, Kartagener's, and TMJ syndrome. Need CT scan to rule out obstruction.
|
|
25yo F develops high fever, myalgias, rhinorrhea, and sore throat.
|
Common cold, due to: influenza virus, rhinovirus, coronavirus, adenovirus, parainfluenza. Rule out bacterial sinusitis, pharyngitis, and allergic rhinitis (history of itchy eyes, nose, and throat).
|
|
25yo F develops high fever, myalgias, and palpable tender neck nodes.
|
Bacterial pharyngitis. No cough or rhinorrhea. Tonsillar exudate may be present. Viral pharyngitis much more common (90%). Group A strep >> other strep, mycoplasma, chlamydia, and neisseria gonorrhea. Diptheria with grey-white pseudomembrane.
|
|
25yo F with itchy eyes, nose, and throat. Pale edematous nasal mucosa.
|
Allergic rhinitis. Seasonal or allergic pattern. Tearing. Mucosa is not erythematous.
|
|
25yo F with purulent nasal discharge, tender face, and toothache.
|
Bacterial sinusitis. Treat with amoxicillin.
|
|
Findings suggestive of Group A strep pharyngitis.
|
Recent exposure, history of infection in past yr, absence of cough, hoarseness, or rhinorrhea, temp > 101, tonsillar exudate, anterior cervical lymphadenopathy.
|
|
Causes of secondary hypertension (5% of all HTN, primary/essential HTN 95%)
|
Aortic coarctation, intrinsic renal dx, renal artery stenosis (young = fibromuscular, old = athero), primary hyperaldosteronism (suspect if hypokalemic and not on diuretic), Cushing's, Pheo,
|
|
1 anatomic, two renal, three adrenal, and four CENTs cause HTN.
|
CENTs = hyperCalcemia, Ethanol or Estrogen (oral contraceptives) most common causes, Neurologic disease = increased ICP, Thyrotoxicosis.
|
|
21yo F develops dramatic increase in creatinine after starting ACE inhibitor therapy for hypertension.
|
Consider renal artery stenosis!
|
|
31yo M with mental status changes and blood pressure of 225/124
|
Hypertensive emergency. Hypertensive urgency = systolic BP > 220. Hypertensive emergency = Urgency + End-organ damage: encephalopathy (ms changes), intracranial hemorrhage, aortic dissection, MI, unstable angina, hypertensive nephropathy.
|
|
HTN treatment: uncomplicated, DM1, CHF systolic, CHF diastolic, isolated systolic HTN, CAD or MI, BPH, pregnancy.
|
beta blocker or diuretic; ACE or diuretic; beta blocker, diuretic, or CCB; diuretic; beta blocker; prazosin; methyyldopa.
|
|
18yo M with painful swollen knee and ipsilateral leg lower leg edema.
|
Ruptured popliteal cyst.
|
|
54yo F with inguinal lymphadenopathy, pelvic symptoms, weight loss and bilateral lower extremity edema. Dry and scaly skin on feet.
|
Lymphedema.
|
|
43yo F with painless edema worse at the end of the day. Varicose veins present. Improves with elevation.
|
Chronic venous insufficiency.
|
|
54yo F with painful thighs and bilateral lower extremity edema following knee replacement surgery.
|
Bilateral DVTs.
|
|
45yo F with tachycardia, bilateral lower extremity edema, and tremor.
|
Pretibial myxedema (Grave's disease)
|
|
12yo M with leg length discrepancy since childhood and ipsilateral lower extremity edema.
|
Congenital venous malformation.
|
|
24yo F with SLE presents with bilateral lower extremity edema.
|
Nephrotic syndrome.
|
|
28yo M with taut, shiny skin and extreme sensitivity to touch of right leg. Edema in the right leg on exam.
|
Reflex sympathetic dystrophy.
|
|
43yo M with lots of tatoos develops peripheral edema and necrotic skin lesions.
|
HCV is associated with cryoglobulins and membranoproliferative glomerulonephropathy.
|
|
45yo F with recurrent infections, nonhealing leg ulcers, history of RA, and splenomegaly on examination.
|
Felty's syndrome.
|
|
Calcinosis, Raynaud's, Esophageal dysmotility, Sclerodactyly, Telangiectasias.
|
CREST
|
|
45yo F with history of PBC with skin thickening of the fingers and difficulty swallowing.
|
CREST. Associated with PBC and primary pulmonary hypertension.
|
|
Causes of chronic cough
|
Postnasal drip > GERD > asthma. Also cigarette use +/- COPD. Less common causes include bronchiectasis, CHF, ACE-I, post-pertussis cough, malignancy, chronic infection usually c systemic symptoms, and psychogenic cough.
|
|
Headache and jaw claudication.
|
Giant cell arteritis. Diagnosis with biopsy, start steroid rx immediately. Large vessel vasculitis.
|
|
26yo Asian F with finger ischemia and arm claudication.
|
Takayasu's arteritis. "Pulseless disease". Diagnosis with aortic arch angiogram.
|
|
32yo M with skin ulceration, hematuria, abdominal pain after eating, joint pain, and right hand weakness.
|
Polyarteritis nodosa (PAN). Necrotizing vasculitis of small and medium muscular arteries. 1/3 associated with HBV, also with HCV. No pulmonary findings!
|
|
35yo M with shortness of breath, fever, maculopapular rash, palpable purpura, and cutaneous nodules. CBC reveals eosinophilia.
|
Churg-Strauss. Granulomatous reaction in medium sized vessels.
|
|
28yo M with recurrent sinusitis, hematuria, and hemoptysis. Has had recurrent fevers, weight loss and arthralgias.
|
Waegener's granulomatosis. C-ANCA positive vasculitis of small arteries. Upper and lower respiratory infections.
|
|
Drug causing palpable purpura.
|
Hypersensitivity vasculitis.
|
|
45yo M with abdominal pain, swollen joints, purpuric rash, and hematuria following URI four days ago.
|
Henoch Schonlein Purpura. Definition = IgA nephropathy plus abdominal pain, join pain, and purpura.
|
|
24yo F with history microscopic hematuria and microalbuminuria, now with gross hematuria following URI.
|
IgA nephropathy
|
|
34yo M with hemoptysis and hematuria.
|
Goodpasture's syndrome. Anti-glomerular basement membrane antibody. (Anti-GBM).
|
|
50yo M with CLL presents with blurry vision, finger ischemia, headache, and lethargy.
|
Monoclonal cryoglobulinemia. Rx with plasmapheresis.
|
|
60yo M with history of IVDA now with arthralgia, purpura, glomerulonephritis, and neuropathy.
|
Mixed cryoglobulinemia. Result of immune complex deposition. Associated with HCV, lupus, and RA.
|
|
35yo M with one year progressive dyspnea. Oxygen saturation drops with ambulation.
|
Idiopathic pulmonary fibrosis or PCP pneumonia. Hallmark of interstitial lung disease.
|
|
Dermatomyositis patients have increased risk of what?
|
Malignancy: colon, lung, breast, and prostate.
|
|
Causes of wheezing
|
CARES: Cardiac asthma (CHF), Churg-Strauss, Allergic bronchopulmonary aspergillosis, Reflux esophagitis (GERD), Exposures (irritants, meds), Embolism, Sinusitis, Strongyloides.
|
|
Causes of obstructive lung disease?
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Asthma, COPD, bronchiectasis, cystic fibrosis.
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Causes of restrictive lung disease?
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Pleural fibrosis, Interstitial (idiopathic, fungal infection: histoplasmosis, sarcoid), neuromuscular (myasthenia gravis, myopathy, Guillain-Barre), alveolar edema or inflammation, BOOP, pleural effusion, kyphoscoliosis, pregnancy, obesity.
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What causes most cases of acute bronchitis?
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Viral > atypical bacteria (Mycopl, Chlamydia, Legionella) > typical bacteria rarely (s. pneumo, h. flu, morexella) > allergic. Acute onset of cough and sputum production s hx of chronic pulm dx and no evidence of pneumonia or sinusitis. No Abs needed.
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Most common immunodeficiency?
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Selective IgA deficiency. Caused by anti-IgA IgG. Recurrent sinopulmonary infections.
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Low IgA, IgG, and IgM. Normal numbers of B cells. Pts 15-30yrs old.
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Common variable immunodeficiency. Associated with autoimmune disease and lymphoid malignancies.
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Recurrent pyogenic infections of skin and lower respiratory tract. Pruritus, coarse facies, keratotic nails.
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Job's syndrome. Hyper-IgE. Autosomal recessive. Abscess, empyema, staph. aureus.
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Thrombocytopenia, eczema, and recurrent infections.
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Wiscott-Aldrich. Depressed cell-mediated immunity, high IgA.
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Low set ears, opportunistic and viral infections, severly sick after live viral vaccine, hypokalemia and hypocalcemia.
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DiGeorge syndrome. Congenital immunodeficiency with no thyroid or parathyroid. 3rd and 4th pharyngeal pouch.
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5yo M without tonsils, recurrent URIs and skin infections, and asymmetric arthritis.
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Bruton's congenital agammaglobulinemia.
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Recurrent staph and strep infections in albino child.
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Chediak-Higashi.
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34yo M with slow onset of cough and pleuritic chest pain several days following resolution of URI.
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Pneumococcal pneumonia. Usually abrupt presentation occurs insidiously following viral respiratory tract infection.
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57yo M with COPD develops pleuritic CP and worsening cough.
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H. flu pneumonia.
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88yo F develops cough, fever, and pleuritic CP.
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S. aureus pneumonia. Seen in ICd and nursing home pts.
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54yo alcoholic presents with productive cough, fever, and lobar consolidation on CXR.
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Aerobic GNR pneumonia.
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19yo F with mild pneumonia and hemolytic anemia.
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Mycoplasma. Prominent extrapulmonary symptoms including: erythema multiforme, myocarditis, erythema nodosum, bullous myringitis, neurological abnormalities.
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23yo M with mild pneumonia and hoarseness with severe pharyngitis.
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C. pneumoniae. Distinguishing feature = hoarseness with severe pharyngitis.
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Atypical pneumonias?
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Legionella, Moraxella, Chlamydia, Mycoplasma.
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Pneumonia requiring hospital admission?
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Two or more lobes, increased A-a gradient or tachypnea, mental status changes, vulnerable patient, homeless patient, very high/low white count.
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45yo M with pedal edema, nocturia, and morning headache.
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Sleep apnea. Symptoms include snoring, daytime hypersomnolence, morning headache, impotence, nocturia or enuresis, pedal edema, exercise fatigue. Exclude hypothyroidism and acromegaly.
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Abdominal Pain due to metabolic / systemic disorders: Puking My Very BAD LUNCH
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Porphyria, Mediterranean fever, Vasculitis, Black widow, Addison's / Angioedema, DKA, Lead, Uremia, Neurogenic (diabetes, syphillis, spinal nerve impingement), hyperCalcemia, Herpes zoster.
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Abdominal pain: RUQ
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liver, gallblader
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Abdominal pain: Epigastric
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stomach, pancreas, duodenum, abdominal aorta
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Abdominal pain: LUQ
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spleen
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Abdominal pain: lower quadrants
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appendix, intestine, ovary, fallopian tubes, testes, kidney, ureters
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Abdominal pain: periumbilical
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small intestine, appendix, abdominal aorta
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Abdominal pain: suprapubic
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bladder, uterus, ovaries, fallopian tubes
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Causes of secretory diarrhea that persists despite fasting?
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Thyrotoxicosis, carcinoid syndrome, colon cancer, colonic polyps, durgs.
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Drugs causing diarrhea?
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Colchicine, Mg-containing antacids, antibiotics, theophylline, lactulose, laxatives.
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Causes of osmotic diarrhea?
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Drugs, pancreatic insufficiency, celiac disease, lactose/fructose intolerance, laxatives.
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Causes of exudative diarrhea?
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(Protein, blood, mucus) Stools with leukocytes and blood. Causes include: Lymphoma, Whipple's disease, collagenous colitis, IBD, ischemic colitis.
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Intestinal motility disorders associated with?
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IBS, DM, narcotic use, systemic sclerosis, fecal impaction, surgery (post-gastrectomy dumping, post-vagotomy syndrome).
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Causes of malabsorption?
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Radiation enteritis, bacterial overgrowth, enteric fistula, ileal resection, short bowel syndrome.
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Diarrheas associated with immunodeficiency?
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Isospora belli, Microsporidia, Cryptosporidium parvum, Giardia lamblia, Strongyloides stercoralis, Entameba histolytica, Mycobacterium-avium-intracellulare complex, Clostridium difficile, CMV.
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What accounts for 50% of cases of diarrhea referred to gastroenterologists?
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Functional diarrhea. No organic cause.
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34yo M presents with low back pain worse with rest and bloody diarrhea.
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Crohn's disease.
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67yo M with CAD and familial hypercholesterolemia presents with bloody diarrhea.
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Ischemic bowel.
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31yo F with diarrhea, weight loss, and skin rash.
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Celiac disease with dermatitis herpetiformis.
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Causes of constipation?
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Neoplasia, strictures, adhesion/rectoceles, drugs (tricyclics, opiates, neuroleptics, antihistamines, CCBs, iron supplements, antacids without Mg), DM, hypothyroid, hypokalemia, hypomagnesemia, uremia, neurologic disorders, IBS, amyloid, scleroderma.
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Type 1 RTA (distal)
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H secretion. Low K. pH > 5.3. Rx: HCO2 + K. Hereditary, amphotericin, collagen vascular disease, cirrhosis, nephrocalcinosis.
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Type 2 RTA (proximal)
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Bicarb reabsorption. Low K. pH < 5.3. Rx: HCO3 + K + thiazide. Hereditary, sulfonamides, carbonic anhydrase inhibitors, Fanconi syndromes.
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Type 4 RTA (distal)
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Aldosterone defiency. High K. pH < 5.3. Rx: Fludrocortisone, K restriction, HCO3. Hyporeninemic with diabetes, HTN, or chronic interstitial nephritis; aldosterone resistance.
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Anion gap metabolic acidosis?
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MUDPILES: Methanol, Uremia, Diabetic ketoacidosis, Paraldehyde, Iron/INH, Lactic acidosis, Ethylene glycol, Salicylates.
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Hyperchloremic metabolic acidosis (no anion gap)?
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Diarrhea, RTA, spironolactone/acetazolamide, TPN
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Respiratory acidosis?
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Foreign body, pneumothorax, flail chest, hypoventilation d/t sedatives/narcs, obstructive/restrictive pulmonary disease, pleural effusion.
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Metabolic alkalosis?
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NaCl responsive = vomiting, villous adenoma, contraction alkalosis, diuretics. Rx IVF + K. Not NaCl responsive = Conn's & Cushing's, adrenal hyperplasia, licorice, Bartter's syndrome. Rx: KCl and spironolactone or acetazolimide (enhance HCO3 excretion)
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Respiratory alkalosis?
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Hyperventilation (anxiety/pain), CVA, head trauma, asthma, PE, CHF, pneumonia, pregnancy, hepatic insufficiency, ASA toxicity, thyrotoxicosis, mechanical ventilation. Rx = treat underlying cause.
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Hyponatremia?
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High osmolality = hyperglycemia or hypertonic infusion. Normal osmolality = Pseudohyponatremia, hyperlipidema, hyperproteinemia. Low osmolality = hypotonic hyponatremia.
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Hypotonic hyponatremia?
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Check FeNa: > or < 1%.
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Hypotonic hyponatremia with FeNa >1%.
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Hypervolemic = renal failure; Euvolemic = SIADH, hypothyroidism, renal failure, drugs; Hypovolemic = diuretics, RTA, adrenal insufficiency, ACE inhibitors.
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Hypotonic hyponatremia with FeNa <1%.
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Hypervolemia = nephrosis, CHF, cirrhosis; Euvolemic = polydipsia; Hypovolemic = vomiting, diarrhea, third spacing, dehydration.
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Treatment fo hypotonic hyponatremia?
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Hypervolemic = salt & water restrict; Euvolemic = salt & water restrict; Hypovolemic = normal saline.
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Hyperkalemia signs and symptoms?
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Intestinal colic, areflexia, weakness, peaked T wave, prolonged QRS and PR, low P.
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Causes of hyperkalemia?
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Cellular shifts: (tissue injury, acidosis, insulin deficiency, drugs including succinylcholine, digitalis, beta-agonists, arginine);
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Decreased excretion: renal insufficiency, drugs (spirlonolactone, triamterene, ACE-I, trimethoprim, NSAIDs), mineralocorticoid deficiency.
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Iatrogenic and spurious: hemolysis, fist clenching, leukocytosis, thrombocytosis.
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Treatment of hyperkalemia?
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C BIG K = Calcium gluconate (cardiac membrane stabilization); Bicarb, Insulin, Glucose; Kayexalate and loop diuretics (furosemide).
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Hypokalemia symptoms?
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muscle weakness, cramps, ileus, hyporeflexia, parasthesias, flaccid paralysis.
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Causes of hypokalemia?
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Linear calcification on x-ray of the knee?
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Pseudogout. Positive birefringent crystals. Associated with hemachromatosis.
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58yo F with long history of RA develops splenomegaly and leukopenia.
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Felty's syndrome.
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FEVER & RASH
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meningococcemia
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septic shock, pustules, organisms on gram stain
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gonnococcemia
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prositutes, urethritis, joint pain with effusion
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typhoid fever
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poor sanitation, prolonged fever, constipation, bradycardia, rose spots
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staph sepsis
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vesicles and bullae, IVDA
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vibrio vulnificus
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raw seafood, lesions on legs > arms, cirrhotics most susceptible
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folliculitis
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hot tubs: pseudomonas; swimmer's itch: schistosomes
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streptococcal infection
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scarlet fever: sandpaper texture of rash, cellulitis, palms peeling
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staph
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Toxic shock = palmar desquamation
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rocky mountain spotted fever
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ascending purpuritic rash on palms and soles
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HIV
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maculopapular rash, viral syndrome
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Diagnosis of amyloidosis?
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Biopsy of abdominal fat pat or rectal biopsy.
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ATPW hypocalcemia?
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Serum Ca and Mg. Serum PTH, 25 and 1,25-D, phosphate, Cl, creatinine, amylase & lipase. Obtain EKG to look for prolonged QT.
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Causes of hypocalcemia?
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HIPOCAL: Hypo-PTH, Infection, Pancreatitis, Overload (rapid IV volume expansion), Chronic renal failure, Absorption abnormality, Loop diuretics.
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Causes of hypercalcemia?
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MISHAP-F: Meds/malignancy, Intox (vit D or A) or Immobilization, Sarcoidosis, Hyper-PTH or Hyperthyroid, Addison's or milk-Alkali, Paget's or Pheochromctoma. Familial hypocalciuric hypercalcemia (benign autosomal dominant condition)
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Symptoms of hypercalcemia?
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abdominal moan, psychiatric groan, kidney stone, and urination zone.
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Most common cause of hypercalcemia?
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malignancy or hyperparathyroidism.
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Sideffect of lithium?
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Hyperparathyroidism: alters setpoint for PTH secretion.
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Thiazide diuretic sideffect?
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hypercalcemia d/t increased renal reabsorption.
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PTH-related peptide secreting tumors?
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breast, lung, renal cell
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Why does sarcoid and other granulomatous disease cause hypercalcemia?
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increased conversion of 25-hydroxyvitamin D to 1,25 in macrophages. Occurs in TB, berylliosis, and lymphoma.
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Most common hyperparathyroidism?
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Solitary adenoma > 80% of cases. Four-gland hyperplasia 10%, multiple adenomas 5%, MENI or II.
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