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53 Cards in this Set
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Neuromuscular effects of hypomagnesemia
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paresthesia, hyperreflexia, muscle spasm, tetany
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major causes of glomerular hematuria after an URI
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Two causes
IgA nephropathy: less than 5d following URI post-streptococcal glomerulonephritis: 10d following pharyngitis |
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Alport's syndrome
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classically presents in young kid with recurrent episodes of hematuria and proteinuria. immunofluorescence shows no immunoglobulins or complement. electron microscopy shows alternating thinning and thickening of capillary loops and splitting of BM.
sensorineural deafness |
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renal toxicity of acyclovir
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in high dose parenteral therapy, it can cause crystalluria which will cause renal tubular obstruction and lead to acute renal failure
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hepatorenal syndrome
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characterized by absence of shock, proteinuria, or other clear cause of renal failure, and failure to respond to a 1.5L nl saline bolus
thought to result from renal vasoconstriction in response to total decreased renal blood flow tx liver transplantation; no meds proven |
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bleeding in a 65 yo. evaluation?
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first with colonoscopy
radioisotope scans typically used for pts with active bleeding where colonoscopy may be limited. colon is more common source of chronic Gi blood loss in asymptomatic pts, and therefore EGD would typically be done only after neg colonoscopy. |
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multiple episodes of thrombosis without a clear precipitating factor?
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raise concern for hypercoagulability due to a genetic defect in a younger pt or a primary malignancy in an older pt
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diarrhea in poorly controlled HIV pt
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cryptosporidium parvum major cause of chronic diarrhea, particularly with CD4< 180
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evaluation of lactose intolerance
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positive hydrogen breath test, positive stool test for reducing substances, low stool pH (think lactic acid!) and increased stool osmotic gap (makes sense). No steatorrhea
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mallory weis tears
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ruptured submucosal arteries of the distal esophagus and proximal stomach 2/2 increased retching
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small intestine bacterial overgrowth
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malabsorption syndrome d/t anatomic or dysmotility disorders (scleroderma!). typically p/w abdominal bloating, flatulence, and diarrhea. weight loss and nutritional deficiencies may occur in severe cases
endoscopy with jejunal aspirate showing >10^5 oganisms/mL is gold standard for dx |
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neutrophilic cryptitis
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present in both Crohn's and UC
bimodal age distribution with peaks at 20 and 60 |
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primary HIV
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p/w mono-like syndrome consisting of fever, night sweats, lymphadenopathy, arthralgias, and diarrhea
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GERD that requires upper GI endoscopy?
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alarm sx (dysphagia, odynophagia, weight loss, anemia, GI bleeding, or recurrent vomiting) or are men age > 50 with chronic (> 5yrs) sx and CA risk factors (eg tobacco use)
all other pts can have an empiric trial of PPI therapy and further evaluation if refractory to therapy |
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sx: glucagonoma, insulinoma, gastrinoma, VIPoma
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glucagonoma: necrotizing dermatitis, weight loss, anemia, and persistent hyperglycemia
insulinoma: rare beta cell tumor that releases insulin and causes hypoglycemia gastrinoma: cause increased gastrin release and multiple gastrin ulcers VIPoma: severe watery diarrhea |
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classic presentation for giardiasis?
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common in areas where sanitary conditions are poor.
etiology: trophozoites adhere to the mucosal surface by adhesive disks and produce malabsorption, which can sometimes be severe and may lead to weight loss. empiric tx with course of METRONIDAZOLE |
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ACD:
NSAID usage in elderly pt with s/s of anemia |
caused by suppression of RBC production by inflammatory cytokines. Commonly occurs in inflammatory arthropathies (RA, lupus) but is not a/w osteoarthritis!
with NSAIDs, think of iron deficiency anemia from chronic blood loss from the GI tract |
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common drugs that cause pancreatitis
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1) diuretics: furosemide, thiazide
2) drugs for IBD: sulfasalazine, 5-ASA 3) immunosuppressive agents: azathioprine, L-asparaginase 4) drugs used by pts with a h/o seizures of bipolar disorder: VPA 5) drugs used by AIDS pts: think about didanosine, pentamidine 6) antibiotics: metronidazole and tetracycline |
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mechanism by which TPN causes gallstones?
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gallbladder stasis
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visceral vs somatic pain in acute appendicitis
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initial periumbilical pain is referred pain and visceral in nature!!; however, pain shifts to the RLQ with involvement of the parietal peritoneum and becomes somatic in nature
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pt with subacute to chronic presentation of abdominal pain, tenesmus, and bloody diarrhea.
also with signs of sepsis. Next step in mgmt? |
In pts with IBD and worsening sx accompanied by signs of sepsis, toxic megacolon!!! should be considered and an ABDOMINAL RADIOGRAPH ordered to confirm dx
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Zollinger ellison syndrome
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gastrin-producing pancreatic tumor!
multiple duodenal ulcers typical, and a jejunal ulcer is almost pathognomonic for this condition. Steatorrhea!!! may develop because increased production of stomach acid inactivates pancreatic enzymes |
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minimal bright red blood per rectum and do not have any risk factors for colon CA. next step in mgmt?
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office-based anoscopy/proctoscopy, particularly in pts less than 50yo
some of most common causes include: hemorrhoids, anal fissure, polyps, proctitis, rectal ulcers and CA |
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see Q. ID 4431
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shingles due to reactivation of varicella zoster virus from a dorsal root ganglion. Pts experience pain and a vesicular rash in a dermatomal distribution. Pain may precede the rash by several days, during which dx may not be apparent.
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IBD colonic mucosa shows what?
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normal colonic mucosa!
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age > 60 with bleeding mixed with stools. no abdominal pain. h/o aortic stenosis
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angiodysplasia!! common cause of recurrent or occult painless lower GI bleeding in patients age > 60yo
reported to cause lower GI bleeding in patients with AORTIC STENOSIS! and END STAGE RENAL DZ! note: hemorrhoids should only be noted on the SURFACE of the stool and is not mixed. |
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intestinal obstruction? when should you resort to surgical mgmt?
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those who develop clinical or hemodynamic instability, fail to improve after initial conservative measures, and/or develop s/s strangulation (fever, tachy, leukocytosis, and metabolic acidosis)
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toxic megacolon mgmt?
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prompt IV steroids, NG decompression and fluid mgmt
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esophageal dysmotility sx
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sticking sensation in the throat and absence of peristaltic waves in lower 2/3 of esophagus, and significant decrease in lower esophageal sphincter tone
think of scleroderma! |
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whipple dz
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multi-systemic illness characterized by arthralgias, weight loss, fever, diarrhea and abdominal pain. PAS-positive! material in the lamina propria of the small intestine is a classic bx finding
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MEN types
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MEN 1: parathyroid, pituitary, and pancreatic
- remember that zollinger-ellison is a pancreatic tumor! MEN2A: medullary thyroid, pheo, and parathyroid hyperplasia MEN2b: medullary thyroid, pheo, marfanoid habitus, and intestinal/mucosal neuromas |
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causes of peptic strictures
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GERD!, also radiation, scleroderma, and caustic ingestions
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D-xylose test
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absorbed by passive diffusion in the proximal small intestine followed by urine excretion. Pts with proximal small intestine dz (ie celiac sprue) will have an abnl D-xylose test due to impaired D-xylose absorption and urinary excretion
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extraintestinal manifestations of UC
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sclerosing cholangitis, uveitis, erythema nodosum, and spondyloarthropathy
severe complications include toxic megacolon and colon CA routine surveillance with UC beginning 8-10 years following dx for prevention and/or early detection of colon CA |
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clues to folate vs vitb12 deficiency
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folate: found in fresh green leafy veggies and liver. folic acid heat sensitive. depleted in 4-5mo
vitb12: strict vegan, store sufficient to last at least 3-4 yrs |
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drugs that can cause esophagitis
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tetracyclines, aspirin and Nsaids, alendronate, potassium chloride, quinidine, and iron
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malignant obstruction of biliary system s/s?
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conjugated hyperbili, elevated alkphos
painless jaundice!, systemic sx (fatigue, weight loss) likely etiologies include: pancreatic adenocarcinoma or cholangiocarcinoma. next step is abdominal imaging (US or CT) with consideration for ERCP if initial testing is neg |
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old person with severe epigastric pain and h/o angina. first work up?
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first do EKG to r/o MI before looking for aortic dissection or other GI pathology
MI can present with epigastric pain, especially inferior and posterior infarctions. |
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endoscopic findings of prominent gastric folds, ulcer located beyond the duodenal bulb
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characteristic of zollinger ellison syndrome (gastrinoma)
all suspected pts should have FASTING SERUM GASTRIN patients with nondiagnostic fasting serum gastrin levels should have a secretin stimulation test done |
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dyspepsia workup
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aged > 55 with new onset sx of dyspepsia and those of any age with alarm sx (weight loss, dysphagia, or persistent vomiting) should be evaluated with upper endoscopy!
other pts should have H. pylori serology testing or empiric tx with PPIs |
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zenker's diverticuli
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most common in elderly males and p/w dysphagia, regurgitation, foul-smelling breath, aspiration, and possibly a palpable mass.
develops immediately above upper esophageal sphincter by herniating posteriorly between the fibers of cricopharyngeal muscle. MOTOR DYSFUNCTION and incoordination are responsible for the problem. contrast esophagram is the test of choice! for confirming dx tx: surgical -> EXCISION AND FREQUENTLY CRICOPHARYNGEAL MYOTOMY |
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suspected achalasia based on sx. next step in mgmt/
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endoscopic eval for to exclude esophageal malignancy at hte esophageal-gastric junction (which can mimic achalasia
treatment involves botulinum toxin and also nitrates/ca channel blockers |
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pellagra
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niacin deficiency characterized by triad of 3Ds: diarrhea, dermatitis, and dementia and if left untreated leading to death
most commonly found among people eating corn-based diets in parts of INdia, Africa, and China also seen in alcoholics, pts with carcinoid syndrome, and hartnup's dz skin rash present in sun exposed areas. |
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pts with carcinoid syndrome are at increased danger of developing what vitamin deficiency?
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niacin!
precursor of serotonin is tryptophan, which is an AA also utilized in synthesis of niacin. |
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ischemic colitis likely to affect which areas of the bowel?
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most common in splenic flexure, bc it is supplied by end arteries. splenic flexure is a watershed line btw the territory of the superior and inferior mesenteric arteries.
two watershed zones in the colon: 1) splenic flexure and 2) recto-sigmoid junction |
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tropical sprue
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pts with malabsorption, along with h/o living in endemic areas for more than one month.
involves the small intestine; the typical bx characterized by blunting of villi with infiltration of chronic inflammatory cells, including lymphocytes, plasma cells and eosinophils |
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SBP
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suspected in any pt with cirrhosis and ascites who p/w low-grade fever, abdominal discomfort, or AMS. Ascitic fluid with PMNs > 250 and positive peritoneal fluid cx confirm dx
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stepwise approach for tx of ascites
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1) sodium and water restriction (< 2L/daily)
2) spironolactone 3) loop diuretic (not more than 1L/day of diuresis) 4) frequent abdominal paracentesis (2-4L/day as long as renal function is oK!! (watch out for hepatorenal syndrome) |
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tumors at head of pancreas
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abdominal pain, weight loss, jaundice, distended gallbladder on exam!! characteristic findings on imaging including intra and extrahepatic biliary tract dilation!!
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octreotide vs propranolol for esophageal varices
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ocreotide: used for active variceal bleeding
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risk factors for a polyp progressing into malignancy
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villous adenoma, sessile adenoma, and size > 2.5cm
only adenomatous polyps are clearly premalignant, but < 1% of such lesions progress to malignancy. Hyperplastic polyps are nonneoplastic and do not require further workup |
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how to spot factitious diarrhea (laxative abuse)
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frequent, watery, nocturnal diarrhea.
dx confirmed with characteristic bx of dark brown discoloration of the colon with lymph follicles shining through as pale patches (melanosis coli) |
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zinc deficiency
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may result from chronic TPN or malabsorption. sx include alopecia, skin lesions, abnl taste, and impaired wound healing
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