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102 Cards in this Set
- Front
- Back
- 3rd side (hint)
cavitation seen only in what kind of TB
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secondary (Ghon complex only in primary)
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odontoma
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most common odontogenic tumor; hamartoma--odontogenic epithelium, odontoblastic tissue
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Ranula
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lg mucocele of salivary gl origin, usually on floor of mouth
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most frequently occurring salivary tumor gland tumor?
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pleomorphic adenoma (benign but often recurs; "mixed")
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pulsion esophageal diverticula vs. traction esophageal diverticular
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pulsion--false, herniation of mucosa through defects in muscular layer; traction--true, result of periesophageall inflammation, scarring, all layers involved
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Zenker diverticulum
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esophageal diverticulum immediately above upper esophageal sphincter
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achalasia due to?
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(persistent contraction of LES, absence of peristalsis--> dilation); due to loss of ganglion cells in myenteric plexus
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Cushing ulcer
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acute gastric ulcer in assoc'n with brain injury
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Menetrier dz
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giant hypertrophic gastritis with extreme enlg'ment of gastric rugae
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is peptic ulcer of stomach a precursor lesion of gastric carcinoma?
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NO
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blood group A assoc'd with what neoplasm
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carcinoma of stomach
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None
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what etiologic factors assoc'd with stomach carcinoma?
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H. pylori; nitrosamines; excessive salt intake; achlorhydria
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Krukenberg tumor
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bilateral involvement of ovaries by metastatic carcinoma of stomach (see signet ring cells)
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variants of stomach carcinoma
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intestinal type-polypoid, assoc'd with h.pylori; infiltrating/diffuse--not assoc'd with h.pylori, leather-bottle stomach
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ulcerated intestinal type stomach carcinoma vs peptic ulcer?
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peptic ulcer--smooth base w/non elevated, punched out margins; carcinoma--irregular necrotic base and firm, raised margins
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peptic ulcer assoc'd with what blood group?
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O
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None
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which peptic ulcer is NOT assoc'd with hypersecretion of gastric acid and pepsin?
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stomach!
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peptic ulcer in JEJUNUM suggestive of?
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Zollinger-Ellison syndrome
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peptic ulcers assoc'd with?
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NSAID use; smokers; Z-E syndrome; primary hyperparathyroidism; MEN type 1
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Meckel diverticulum a remnant of what?
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embryonic vitelline duct (may contain ectopic gastric, duodenal, colonic, pancreatic tissue)
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complicatons/assoc'ns of Meckel diverticulum?
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usually asymptomatic but if ectopic gastric tissue, may ulcerate; intussusception; volvulus
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cobblestone appearance of GI mucosa assoc'd with?
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Crohn's
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celiac dz most commonly assoc'd with what malignancy?
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enterophaty-type T cell lymphoma
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Name the dz: distinctive PAS+ macrophages in intestinal mucosa
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Whipple dz (Tropheryma Whippelii)
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carcinoid syndrome
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get cutaneous flushing, watery diarrhea, ab cramps, bronchospasm, R heart valvular lesions; happens if mets to liver
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carcinoid most frequently where?
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appendix. if anywhere else, tends to mets to liver-->get carcinoid syndrome
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ischemic bowel dz most often where?
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splenic flexure and rectosigmoid junction (watershed areas)
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angiodysplasia
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tortuous dilation of small vessels spanning intestinal (sub)mucosa; common cause of otherwise unexplained lower bowel bleeding
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pseudomembranous colitis due to?
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EXOTOXIN of C. difficile; get fibrinous necrosis of superficial mucosa
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flask shaped ulcers in colon--> ?
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amebic colitis (Entamoeba histolytica)
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Peutz-Jeghers polyps
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hamartomatous polyps; part of syndrome; get melanotic accumulations in mouth, hands, genitalia; not malignant but assoc'd with inc'd propensity for malignancy at other sites
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types of adenomatous polyps
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(true neoplasms) tubular--most common; tubulovillous; villous--least common, sessile and velvety
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which kind of adenomatous polyp most likely to turn malignant?
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villous adenoma
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tubular adenomas
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small pedunculated polyps with malignant foci
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Gardner syndrome
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AD, numerous adenomatous polyps along with osteomas and soft tissue tumors
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Turcot syndrome
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adenomatous polyps and tumors of CNS
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significance of CAE in colon cancer?
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nonspecific marker so best for following course of dz
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most common appendicieal neoplasm?
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carcinoid
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Gilbert syndrome
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common familial D/O; modest elevation of sr UNCONJUGATED bilirubin due to dec'd BR uptake by liver and dec'd activity of glucuronyl trasferase
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Crigler-Najjar syndrome
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severe familial D/O; UNCONJUGATED hyperbilirubinemia due to glucuronyl trasnferase deficiency (Amish!);
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Dubin-Johnson syndrome
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AR, CONJUGATED hyperbilirubinemia due to defective BR transport; get striking brown to black discoloration of liver due to deposition of very dark granules
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How is Rotor Syndrome different from Dubin-Johnson syndrome?
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both are conjugated hyperbilirubinemias due to BR transport problem but no abnl pigmentation of liver in Rotor
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which hepatitis viruses assoc'd with hepatocellular carcinoma?
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Hep B, C
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How is Hep A spread?
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(ssRNA, picornavirus) fecal-oral
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infected HBV hepatocytes have what appearance?
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"ground glass"
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significance of HBeAg?
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closely correlated with viral infectivity
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Which hep virus requires prior or concurret infection with HBV and in what population seen most?
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Hep D, IV drug users (makes more fulminant course)
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How distinguish autoimmune hepatitis from other forms (HBV, HCV)
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both viral and autoimmune-> very high ALTS (1000s!); but autoimmune has hypergammaglobulinemia, anti-smooth muscle Ab
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DDx for ALT>1000 U/L
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acute viral hepatitis, drug toxicity (acetaminophen!), shock liver, autoimmune
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neonatal hepatitis characterized by?
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giant cell transformation of hepatocytes; bile pigment of prominent w/i canaliculi and hepatocytes
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hepatic component of yellow fever characterized by?
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(arbovirus) midzonal hepatic necrosis
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ingestion of Echinococcus granulosus--> ?
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hydatid dz of liver; lg parastitic cyts invade liver
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fatty liver of pregnancy
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microvesicular fatty liver; acute hepatic liver failure in 3rd trimester; high mortality
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3 causes of microvesicular fatty liver
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1. Reye syndrome; 2. fatty liver of preggers; 3. tetracycline toxicity
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alcoholic hepatitis assoc'd with what sort of fibrosis?
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irreversible fibrosis that characteristically surrounds CENTRAL vein (perivenular fibrosis)
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Hobnail liver
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scarred shrunken liver, in late stages of cirrhosis
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primary biliary cirrhosis vs primary scleroris cholangitis
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PBC--women, inc'd AP, AMA+, dx by liver bx, tx: ursodeoxycholic acid; PSC--IBD, inc'd AP, AMA-, dx by cholangiography, tx: none
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asymptomatic increase in AP in pt with IBD, think?
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PSC
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middle aged woman with severe obstructive jaundice, itching, hypercholesterolemia and inc'd AP--?
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PBC
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CNS involvement in Wilson dz?
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Cu deposition in basal ganglia-->extrapyramidal motor signs)
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hepatorenal syndrome
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functional renal failure (nl kidneys) characterized by profound Na retention, uremia, oliguria, usually w/ascites
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Budd-Chiari syndrome
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thrombotic occlusion of major hepatic veins (post hepatic portal HTN); ab pain ,jaundice, hepatomegaly, ascites, eventual liver failure
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hepatic adenomas--assoc'd with? big concern?
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OCP; if subcapsular, may rupture-->severe intraperitoneal hemorrhage
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what carcinoma assoc'd with aflatoxin B1?
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hepatocellular carcinoma
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cholangiosarcoma assoc'd with?
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clonarchis sinensis (liver fluke), PSC, late complications of throium dioxide, NOT HBV or cirrhosis!
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strawberry gallbladder
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(cholestrolosis); yellow cholesterol containing flecks in mucusal surface; NOT assoc'd with inflamm changes or cholelithiasis
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most common primary tumor of gallbladder?
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adenocarcinoma
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Courvoisier law
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tumors that obstruct common bile duct will cause enlarged distended gallbladder; obstructing stones do not
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4 big systemic effects of the released cellular components in acute pancreatitis
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1. resp failure (PLA2 degrades surfactant); 2. subdiaphragmatic inflamm; 3. shallow respirations (b/c of pain); 4. hemorrhage
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#1 predisposing factor for chronic pancreatitis?
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alcohol use (also, CF; gld std dx: MRI with MRCP)
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pancreatic carcinoma usually where?
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in head-->obstructive jaundice
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carcinoma in pancreatic tail-->
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possible pancreatic islet destruction and secondary DM
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None
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hyperhydramnios assoc'd with?
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duodenal atresia, TEF
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Name the dz: thickened gomerular capillary walls, subepi immune complex deposition, "spike and dome"
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memranous glomerulonephritis (a major primary cause of nephrotic syndrome)
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Kimmelstiel-Wilson nodules assoc'd with what renal dz?
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diabetic nephropathy (nodular accumulations of mesangial matrix material)
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renal amyloidosis characterized by
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subendothelial mesangial amyloid deposits and distinctive fibrillary pattern
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types of lupus nephropathy (WHO)
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type 1-no renal involvement; 2--mesangial form; 3--focal proliferative; 4--diffuse proliferative (prototype, most severe); 5--membranous (indistinguishable from membranous GN)
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4 clinical findings of nephritic syndrome
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1. oliguria; 2. azotemia; 3. HTN; 4. hematuria
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what kind of strep usually --> post strep GN?
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group A beta hemolytic
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Name the dz: nepritic syndrome, pneumonitis w/hemoptisis, 20-30y/o male
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Goodpasture syndrome (anti glomerular BM)
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mutation in alpha5 chain of type IV collagen--> ?
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Alport syndrome (hereditary nephritis assoc'd with nerve deafness and ocular d/o)
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Berger dz
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IgA nephropathy, v common, usually benign recurrent hematuriain kids following infection
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"tram track" appearance of glomerular BM--> ?
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membranoproliferative glomerulonephritis (mostly type 1; mesangial matrix expands into glom cap loops)
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types of membranoproliferative glomerulonephritis
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1--v. striking tram track; II--dense deposit dx
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pathognomonic finding for acute pyelonephritis?
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white cell casts in urine
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acute drug induce interstitial nephritis most often due to?
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penicillin derivatives (methicilin!); NSAIDS; diuretics
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renal papillary necrosis most often assocd with what a) drug, b)disease
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a) phenacetin + other analgesincs; b) DM
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is acute tubular necrosis reversible?
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yes. necrotic tubular cells can be replaced in ~2 wks
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Fanconi syndrome
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manifestation of generalized dysfunction of proximal renal tubules; clinically--glycosuria, hyperphosphaturia, aminoaciduria, systemic acidosis
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Hartnup dz
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genetic defect--impr'd tubular reabsorp. of tryptophan. can lead to pellagra like symptoms (vit B3 def)
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coarse, asymmetric corticomedullary scarring indicative of?
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chronic pyelonephritis
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thyroidization of kidney
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seen in chronic pyelonephritis; atrophic tubules contain eosinophilic proteinaceous casts
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diffuse renal cortical necrosis most often assoc'd with?
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obstetric catastrophes (placental abruption) or septic shock
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staghorn calculi
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ammonium magnesium phosphate stones in renal pevis and calyces, when urine alkalinized by proteus or stpah (urease +)
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when does adult polycystic kidney dz usually manifest?
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congenital but usually see clincally 15-30y/o
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uremic medullay cystic dz
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(nephronophtisis) v. serious but uncommon ; cysts in MEDULLA of kidney
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multiple renal cysts, glomerular atrophy, scarring and inc'd risk of renal cell carcinoma--?
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acquired cystic dz; assoc'd with long term dialysis
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flank pain, palpable mass, hematuria, polygonal clear cells on histo--?
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renal cell carcinoma (most common renal malignancy, assoc'd with vHL-csome3)
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WAGR complex
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Wilms tumor, Aniridia, Genitourinary malformations, mental-motor Retardation
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Denys-Drash syndrome
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WT-1 gene abnl, intersexual D/O, nephorpathy, Wilms tumor
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Beckwith-Wiedemann syndrome
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ex of genomic imprinting! (mom); WT-2 del; Wilms tumor, hemihypertrophy, macroglossia, organomegaly, neonatal hypoglyceima
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transitional cell carcinoma in renal PELVIS assoc'd with?
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phenacetin abuse
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