Gastrointestinal Flashcards

1
Q

Anal fissue etiology, RF, and sxs

A
  • irritation caused by trauma to anal canal results in increased resting pressure of internal sphincter - ischemia in region of fifssure and poor healing of injury
  • MC in 30-50s, M=F
  • Primary: local trauma, pooping probs, anal sex, SVD
  • Secondary: previous anal surgery, IBD (Crohn dz), TB, sarcoidosis, malignancy, HIV, syphilis, chlamydia
  • MC site: posterior anal midline, below or distal to dentate line (where transition zone becomes squamous epithelium)
  • Sxs: tearing pain with defecation, pruritis, BRB,
  • signs: superficial laceration, in chronic can see external skin tags and hypertrophied anal papillae at proximal end
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2
Q

Anal fissure dx and tx

A
  • dx: endoscopy (if bleeding beyond 2mos tx), sigmoidoscopy if <50yo with no FH colon cancer, colonoscopy if suspician for Crohn dz
  • tx: acute heals in 6wk - fiber and water, sitz baths, topical anesthetic, vasodilator (nifedipine, NTG), stool softeners or laxative
    • if failed tx/chronic: botox, lateral sphincterotomy (gold standard - may cause incontinence)
  • Prevention: proper hygiene - keep dry and wipe with soft cotton or moist cloth, high fiber, high water, dont strain while pooping, avoid trauma to anus, prompt tx of D
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3
Q

Cholelithiasis

A
  • Etiology: stones in gallbladder, pain 2ary to contraction against obstructed duct; 3 types:
      1. cholesterol (yellow/green dt obestiy, DM, HLD, mult gest, OCP, Crohn, ileal resection, old, native american, cirrhosis, CF)​
      1. Pigment (black): hemolysis (SS< thalassemia, spherocytosis, artificial valve), alcoholic
      1. Pigment (brown): in bile ducts dt biliary tract infxn
  • sxs: most asx, biliary colic (RUQ or epigastric), pain after eating and night, boas sign (R subscap pain)
  • dx: RUQ US (high sens/spec if >2mm), CT scan and MRI
  • tx: no tx necessary if asx, elective cholecystectomy for recurrent bouts
  • complications: cholecystitis, choledocholithiasis, gallstone ileus, malig
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4
Q

acute cholecystitis

A
  • obstruction of cystic duct (not infxn) - leads to inflamm of GB wall
  • sxs: RUQ or epigastric pain lasts a few days, may radiate to shoulder or scap, N/V, pruritis, clay-colored stools, dark urine
  • signs: RUQ TTP, rebound in RUQ, Murphy sign, hypoactive bowel sounds, low fever, leukocytosis, jaundice
  • dx: RUQ US, HIDA when US inconclusive, CT scan
    • Labs: elevated ALK-P and GGT, elevated conjugated bili
  • tx: admit, IVF, NPO, IVabx, analgesics, correct lytes, cholecystectomy (first line)
    • 70% recurrence if left untreated
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5
Q

Choledocholithiasis, cholangitis, primary sclerosing cholangitis, primary biliary cirrhosis

A
  • Choledocho: stones in CBD
    • dx: RUQ US (first line), ERCP (gold standard - dx and tx)
    • tx: ERCP with sphincterotomy and stone extract with stent placement, lap choledocholithotomy
  • Cholangitis: infxn biliary tract 2ary to obstruction, CHARCOT TRIAD (RUQ pain, jaundice, fever), REYNOLD PENTAD (RUQ pain, jaundice, fever, HoTN, AMS)
    • dx: RUQ US (first line), CBC, bili, ERCP (definitive, but not used in acute cases)
    • tx: decompress via PTC or ERCP, bust be afeb 48h for ERCP/PTC so blood cultures, IVF, abx and decompress in the mean time
  • Primary sclerosing: chonic idiopathic, likely autoimmune, strong correlation with ulcerative colitis, insidius, progressive jaundice, itching, fatigue, malaise
    • dx: ERCP and PTC
    • tx: liver transplant, cholestyramine - sxatic relief
  • Biliary cirrhosis: chronic, intrahepatic bile duct destruction, autoimmune, similar sxs to primary sclerosing
    • dx: elevated alkphos, +AMA, LIVER BX CONFIRMS DX
    • tx: cholestyramin, Ca, bisphos, vitD for sxs; ursodeoxycholic acid slows progress; liver transplant curative
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6
Q

Cirrhosis

A
  • fibrosis, widespread nodules in liver, irreversible when advanced
  • distortion of liver anatomy causes: portal HTN (dec blood flow through liver - causes ascites, periph edema, splenomeg, varicose veins), hepatocellular failure (dec albumin synth and clotting factor synth)
  • Child pugh scores estimates hepatic reserve (A=mild, C=most severe)
  • MCC of cirrhosis: alc liver disease
    • second MCC: chronic hepB and C infxn
  • MCC of liver dz: nonalcoholic fatty liver dz
  • chronic liver dz: ascites, varices, hemorrhoids, gynecomast, test. atrophy, palmar erythema, spider angiomas, caput medusae)
  • Monitor labs q3-4mo
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7
Q

Colorectal cancer

A
  • most from adenomas (endoluminal adenocarcinomas), Villous > tubular adenomas
  • CRC = MCC LBO in adults
  • RF: >50yo, polyps, hx CRC, IBD (UC), Fhx, diet (high fat, low fiber)
  • sxs: abd pain, bowel habit change, wt loss, hematochezia (asx, unexplaine iron def., mostly in advanced states)
    • R sided: obstruction less common, melena, occult blood, IDA, no bowel habit changes, Triad (anemia, weak, RLQ mass)
    • L sided: obstruction more common dt smaller lumen, change in bowel habits (alternating const/D, narrowing of stools, hematochezia
  • dx: colonoscopy
  • tx: surgery, chemo + radiation, follow w/ guaiac, annual CT of abd/pelv, CXR up to 5y, colonoscopy at 1y, then q3y, CEA levels q3-6mo
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8
Q

Familial adenomatous polyposis

A
  • autosomal dominant (100s polyps in colon), 20-30yo
  • RF: colon CA, thyroid CA, gastric CA, meduloblastoma, duodenal ampullary carcinoma
  • sxs: >100 cumulative colorectal adenomas or hx of adenomas in combo with extracolonic features (duodenal or ampullary adenomas, desmoid tumors, papillary thyroid CA, congen hypertrophy of retinal pigment epith, epidermal cysts, osteomas)
  • complications: IDA
  • dx: endoscopy at 25-30yo (random sampling of fundic gland polyps)
  • tx: prophylactic colectomy (large or high grade dysplasia, annual endoscopy of rectum, ileostomy eval q1-3y), screen thyroid annually
  • risk of CRC 100% by 30-40yo
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9
Q

Hemorrhoids

A
  • varicose veins of anus and rectum
  • RF: const/straining, preg, portal HTN, obesity, prolonged sitting or standing, anal intercourse
  • sxs: BRBPR (painless, associated with bowel mvmnt, pruritis, fecal soilage, rectal prolapse
  • dx: anoscopy if BRBPR or suspected thrombosis
  • tx: sitz bath, ice, bed rest, stool softeners, high fiber/fluid, topical steroids
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10
Q

external hemorrhoids

A
  • dilated veins arising from inferior hemorrhoidal plexus distal to dentate
  • sxs: asxatic unless thrombosed (sudden, painful swelling, lasts several days, then subsides)
  • tx: conservative (sitz bath, ice, stool softeners, etc.)
    • rubber band ligation: if protrudes with defecation, enlargement, or bleeding - for stages 1-3 nonresponsive
    • closed hemorrhoidectomy: for permanently prolapsed (stage 3-4 chronic bleeding or stage 2 acutely thrombosed; eternal dont require surg management unless thrombosed or lare and sxatic)
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11
Q

Internal hemorrhoids

A
  • dilated submucosal veins above dentate line
  • thrombosed: increased with def and sitting; tender, swollen, bluish ovoid mass
  • sxs: painless rectal bleeding, bulging perianal mass w/ straining; when prolapsed, causes mild fecal incont, mucous d/c, wetness, sensation of fullness
  • signs: bulging purplish-blue
  • tx: same as external hemorrhoids
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12
Q

Thrombosed hemoorhoids

A
  • MC with external hemorrhoids
  • sxs: painful defecation, BRBPR, pruritis
  • signs: palpable mass, perianal swelling, acutely tender
  • dx: anoscopy
  • tx: conservative unless persistent or present w/in 72h from onset of pain
    • Surgery = definitive
  • complications: internal hem can become prolapsed, strangulated, and develop gangrenous changes
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13
Q

grades of hemorrhoids and tx

A
  • Grade I: vizualised on anoscopy and may bulge into lumen, but dont prolapse below dentate
    • tx: conservative or rubber band; surg for recurrent or bleeding external
  • Grade II: prolapse with defecation but reduce spontaneously
    • tx: conservative or rubber band; surg for recurrent or bleeding external
  • Grade III: prolapse with defecation, require manual reducation
    • tx: rubber band (initial), sclerotx for sxatic internal (indicated grades I-II bleeding internal or pts on anticoags), surgery recommended (definitive)
  • Grade IV: irreducible and may strangulate
    • tx: requires surgical tx (excision, hemorrhoidectomy)
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14
Q

Colorectal cancer screening

A
  • begin 50yo, continue until 75yo
  • FOBT qy
  • start screening 10y younger than age of dx of youngest affected relative
  • Flexible sigmoidoscopy: q5y combined with FOBT q3y
  • Colonoscopy: q10y (q5y for pts with single 1st degree relative dx with CRC or advanced adenoma)
  • Average risk = pts with no or 1 1st deg relative dxed >/= 60yo with CRC or advanced adenoma, never had CRC or polyp, IBD, abd radiation for childhood CA
  • High risk = 1 1st deg relative dxed w/ CRC <60yo, or 2 1st deg relatives w/ CRC or advanced adenomas
    • for these ppl, colonoscopy q5y beginning age 40 or 10y younger than youngest dx
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15
Q

PUD

A
  • Causes: H. pylori, NSAIDs, Zollinger-Ellison (acid hypersecretion)
    • other causes: smoking, ETOH, coffee, stress, dietary factors
  • sxs: epigastric pain (aching, gnauwing, nocturnal sxs, effect of food variable), N/V, early satiety, wt loss
  • dx: endoscopy (required for dx), barium swallow, H. pylori Ag (Abs to H. pylori can remain elevated for mos-yrs after infxn gone, false negs with PPI, pepto, abx), biopsy (GOLD STANDARD), urea breath test, gastrin measurement (zollinger)
  • tx: supportive (dc NSAIDs, stop: smoking, alc, stress, eating before bed, coffee), acid suppression (H2, PPI (most effective), antacids, eradicate H. pylori infxn (amox + carith + PPI (or carith + flagyl), OR pepto + tetracyc + flagyl + PPI), cryoprotection (sucralfate, misoprostol), surgical (truncal vagotomy for hem, perf, obst, failure of meds)
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16
Q

duodenal vs gastric ulcers

A
  • Duod: MC <40yo, 70-90% H. pylori caused, NSAIDs, relieved with eating, nocturnal pain more common
  • Gast: MC >40yo, 60-70% H. pylori caused, smoking, eating can make pain worse (anorexia and wt loss)
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17
Q

Gastritis

A
  • Acute: NSAIDs, ASA, H. pylori, alc, smoking, caffeine, stress
    • sxs: asx or epigast pain, dyspepsia, abd pain
    • dx: upper GI endoscopy w/ bx, urea breath test, H. pylori Ag
    • tx: stop NSAIDs, empiric tx w/ acid suppress., 4-8wks PPI, if H pylori + tx with abx
  • Chronic: MCC = H. pylori
    • sxs: asx, epigastric pain similar to PUD, N/V/anorexia = rare
    • dx: upper GI endoscopy w/ bx, urea breath test, H. pylori Ag
    • tx: triple tx (PPI + 2 abx) x2wks or quad tx (PPI + pepto + 2 abx) x1wk
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18
Q

Gastroenteritis causes

A
  • Acute viral, traveler’s D, salmonella, shigella, E. coli (enterohemorrhagic), E.coli (enteroinvasive), cholera
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19
Q

acute viral gastroenteritis

A
  • Causes: NORWALK, rotavirus, enterovirus
  • Duration: 48-72h
  • Transmission: fecal-oral
  • MCC ACUTE DIARRHEA
  • sxs: myalgias, malaise, low fever, HA, watery D, abd pain, N/V
  • dx: fecal leuks (none), hypokalemia and met acidosis
  • tx: supportive, look for similar illness in family
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20
Q

Traveler’s diarrhea

A
  • Cause: food/water w/ fecal matter
  • Etiology: ETEC, Campylobacter, Salmonella, Shigella
  • RF: travel destination, occurs in first 2 wks of travel, lasts 4d w/out tx
  • sxs: 3+ unformed stools in 24h w/ at least 1 of following:
    • fever, N, V, abd cramps, tenesmus, bloody stools
  • Complications: dehydration (MC), Guillain-Barre, Reiter syndrome
  • dx: fecal leukocytes, C. diff toxin, 3 stool samples for ova and parasites, bact. stool cx, FOBT
  • tx: empiric (cipro x1-3d), campylobacter and shigella = FQ (FQ resistant, children, preg = azithro), Bismuth subsalicylate (not for pts taking anticoag, causes black tongue, dark stools, tinnitus, Reye syndrome in children)
  • Prophylaxis: proph with FQ = 90% effective
21
Q

Salmonella

A
  • Duration: 1wk
  • Transmission: food, water, fecal-oral
  • Incubation: 5d-2wk (typhoid)
  • sxs: inflamm D, N/V, sxs appear 24-48h after ingesting food (Salmonella typhi presents as C), possible fever
  • dx: fecal leuks +, C. diff toxin and cx, 3 stool sample for ova and parasites, bact. stool cx, hypokalemia and met acidosis
  • tx: cipro
22
Q

Shigella

A
  • Duration: 1wk
  • Transmisison: fecal-oral, MC in developing countries, children <5
  • sxs: abd pain, inflamm D, mucoid and bloody stool, N/V (less common), tenesmus (feeling like u need to constantly poop), poss fever
  • dx: fecal leuks +, C diff toxin, 3 stool samps for ova and parasites, bact. stool cx, hypokalmeia and met acidosis, produces largest quantity of fecal leuks than any other gastroenteritis
  • tx: TMP/SMX (bactrim)​​
23
Q

E. coli

A
  • Enterohemorrhagic E. coli (O157:H7)
    • consumption of undercooked ground beef, Shiga-like toxin
    • Onset: 12-60h; Duration: 5-10d
    • sxs: water, voluminous nonbloody D w/ N/V, can lead to dysentery (bloody)
    • dx: no fecal leuks
    • tx: abx not recommended unless severe
    • complication: hemolytic uremic syndrome
  • Enteroinvasive E. coli
    • Source: food
    • Onset: 5-15d; Duration: 1-5d
    • sxs: cramping, watery D
    • dx: fecal leuks +
    • tx: pepto, imodium, hydration
24
Q

Cholera

A
  • acute diarrheal dz, profound rapidly progressive dehydration and death
  • protein enterotoxin produced by orgs as it colonizes
  • consumption of contaminated shellfish
  • Onset: 24-48h after consumption
  • sxs: watery diarrhea “rice water stool” dt action of cholera toxin
  • signs: fishy odor
  • tx: tetracycline, FQs, or macrolide, oral rehydration
25
Q

Acute pancreatitis

A
  • inflamm from prematurely activated enzymes (autodigestion)
  • Causes: ETOH, gallstones, post ERCP, viral inxn, drugs, scorpion, pancreatic CA, hyperTG, hyperCa, uremia, blunt trauma (MC in kids)
  • Mild (MC): abd pain, epigastric, radiates to back, steady, dull, severe, worse supine and after meals, N/V/anorexia
  • signs: fever, tachycard, HoTN, leuks, epigast TTP, abd distention, dec bowel sounds,
    • hemorrhagic pancreatitis: Gray turner sign (flank), cullen sign (periumbilical), fox sign (inguinal ligament)
  • dx: serum amylase - nonspec, absence dosnt ro, 5xULN, norm 48-72h after, serum lipase (more spec: 5xULN), LFTs, hyperglycemia, hypoxemia, leuks, Ranson criteria (gluc, Ca, hematocrit, BUN, ABG, LDH, AST, WBC), KUB, abd US, CT scan (confirmatory), ERCP
  • tx: bowel rest, IVF, pain control
    • if severe: ICU admit, enteral nutrition in first 72hrs through NJ tube
  • Complicaitons: pancreatic necrosis, pancreatic pseudocyst
26
Q

Chronic pancreatitis

A
  • peristent inflamm - fibrosis and alt of ducts = irreversible
  • causes: chronic ETOH
    • other: hereditary, tropical, idiopathic
  • sxs: severe epigastric pain, N/V, aggravated by drinking/eating, radiates to back, wt loss dt malabsorption, ETOH, DM, steatorrhea dt malabsorption
  • dx: CT, KUB, ERCP (GOLD STANDARD): serum amylase and lipase not elevated, stool elastase = most sens/spec for panc insuff (LOW)
  • tx: pain meds, NPO, panc enzymes, H2 blockers, insulin, no ETOH, frequent small meals, Pancreaticojejunostomy or pancreatic resection (whipple)
  • Complications: narcoti addiction (MC)
  • Malabsorption: late manifestation, pseudocyst, CBD obst, B12 malabs, effusions, panc CA
27
Q

Inflammatory bowel disease

A
  • Ulcerative colitis, Crohn dz, Ischemic colitis
28
Q

Ulcerative colitis

A
  • Chronic inflamm of colon or rectal mucosa (muc . and submuc involvment only), any age, MC = rectum and L colon
  • SMOKING IS PROTECTIVE
  • sxs: gradual or abrupt onset LLQ pain, tenesmus (MC), hematochezia w/ pus, frequent small BMs, fever, wt loss
    • extraintest sxs: scleritis, episcleritis, 1ary sclerosing cholang., erythema nodosum, pyoderma gangrenosum, ankylosing spond.
  • dx: anemia, inc ESR, low serum albumin, ANCA + (60-70%), KUB, cx for c. diff, O and P, fecal leuks + (in UC, ischem colitis, infxs D), colonoscopy (no skip lesions, avoid in acute dz dt risk perf or toxic megacolon), sigmoidoscopy
  • tx: topical or PO sulfasalazine, 5-ASA enema, steroids, immunosuppress, Proctocolectomy (curative, indicated in severe dz, toxic mega, obst, hemorrhage, etc.)
  • complications: IDA, hemorrhage, lyte imbalance, colon cancer, PSC, toxic mega (leading COD)
29
Q

Crohn Dz

A
  • inflamm affecting ANY PART of GI (mouth-anus), MC is small bowel. Unpredictable flares, chronic granulomatous inflamm, transmural inflamm - lead to fistulization, submucosal inflamm
  • MC = terminal ileum and cecum
  • Gradual onset: D (no blood), wt loss dt malabs, RLQ pain, N/V, aphthous oral ulcers, uveitis, arthiritis, erythema nodosum, cholelith, nephrolith
  • Complications: fistula, abscess, transmural thickening and inflamm
  • dx: abd CT (inflamm through wall at ileocecal junction, mesenteric fat wrapping, colonoscopy with bx, cobblestone appearance, skip lesions, RECTAL SPARING
  • tx: Sulfasalazine (mesalamine, 5-ASA), prednisone for acute exacerbations, metronidazole, immunosuppression, cholestyramine
    • Surgery: dt complications (SBO MC, fistulae, perf, abscess)
    • IV nutrition
    • supplement with B12, folate, and vitD
    • stop smoking
    • tx efficacy dec w/ advancing dz, recurrence common after surg
30
Q

Hiatal hernia

A
  • Sliding (type I): >90%, GE junction and stomach herniate into thorax through esophageal hiatus, associated with GERD
    • sxs: asx, heartburn, CP, dysphagia
    • dx: barium upper GI, upper endosc.
    • tx: antacids, small meals, elevation of head of bed
    • complications: GERD, reflux esophagitis, aspiration
  • Paraesophageal (type II): <5%, stomach herniates into thorax through esophageal hiatus, but GE junction does not
    • sxs: can be strangulated, enlarge with time, does NOT cause GERD
    • tx: elective surg
    • complications: obstruction, hemorrhage, incarceration, strangulation (life threatening)
31
Q

Mallory Weiss vs Boerhaave syndrome

A
  • Mallory-Weiss: mucosal tear at (or just below) GE junciton dt vomiting (like in binge drinkers)
    • sxs: after repeated episodes of vom., hematemesis, painful
    • dx: upper endoscopy
    • tx: surgery or angiographic embolization
    • Most resolve spontaneously (90%)
  • Boerhaave: transmural ruptured esophagus dt vomiting
    • sxs: retrosternal CP, odynophagia, fever, HoTN, tachypnea, Hamman’s sign (mediastinal crackling)
    • dx: gastrografin swallow (water soluble contrast preferred when perf suspected)
    • tx: surgery for thoracic perf, abx for cervical perf
32
Q

GERD

A
  • inappropriate relaxation of LES (decreased tone), retrograde flow of stomach contents into esophagus, dec esoph motility, gast outlet obst., hiatal hernia (common)
  • dietary RF: ETOH, tobacco, choc, high fat foods, coffee
  • Complications: barretts esophagus (squamous ep → columnar), dental erosion, laryngitis, pharyngitis, recurrent PNA, esophageal stricture
  • sxs: heartburn, dyspepsia - retrosternal pain, burning shortly after eating, worse with lying down after meals, mimics cardiac CP, regurg, waterbrash (reflex salivary hypersec.), hoarseness, sore throat, globus sensation, early satiety
  • dx: barium study (IDs complications, but not dx), endoscopy w bx (if refractory to tx), 24-h pH monitor (GOLD STANDARD), manometry
  • tx: diet changes (no fat, orange juice, coffee, ETOH, choclate, large meals, smoking), antacids after meals and @ bedtime
    • phase II: add H2 blocker
    • phase III: switch to PPI
    • phase IV: add promotility (metoclop or regland, bethanechol)
    • phase V: H2 + promotility + PPI
    • phase VI: antireflux surg
33
Q

Irritable bowel syndrome

A
  • changes in consistency and frequency of stool without abnl findings on colonoscopy, sigmoid colon MC location, exacerbations with stress or menses, W > M, beings early to mid adulthood, psychiatric sxs precede bowel sxs, worse with stress
  • sxs: present at >/= 3mo, change in frequency or consistency of stool (D or C or both), Cramping abd pain (relieved by def or worse with food), dyspepsia, bloating or feeling abd distention (PP urgency), urinary freq (common in W)
  • signs: sigmoid TTP, hyperresonance
  • dx: everything normal, Dx of EXCLUSION
  • tx: loperamide for D, colace, psyllium, cisapride for C, tegaserod maleate (Zelnorm), Rifaximin (xifan)
  • Avoid dairy and excess caffeine
34
Q

Infectious, pill induced, eosinophilic, radiation, corrosive esophagitis

A
  • infectious: AIDS, organ transplant, leukemia, lymphoma; MC pathogens = candida albicans, herpes, CMV
    • sxs: odynophagia, dysphagia, substerna CP, oral thrush, CMV infxn at other sites, oral ulcers
    • dx: endoscopy w/bx
    • tx: fluconazole (candida), Ganciclovir (CMV), HAART (AIDS), sxatic tx or acyclovir (herp)
  • pill induced: MC = alendronate, clinda, doxy, iron, NSAIDs, KCl, quinidine, tetracycline, bactrim, vitC
    • sxs: odynophagia, dysphagia, severe retrosternal CP
    • dx: endoscopy (shallow or deep ulcers)
    • prevention: take with water, remain upright x30mins
  • eosinophilic: hx food allergies, asthma, atopic derm
    • sxs: dysphagia, impaction (food stuck @ lower esoph.)
    • dx: upper endosc., bx (eosinophil inflamm)
    • tx: topical steroids (budesonide)
  • radiation: radiosensitizing drugs = doxorubicin, bleomycin, cyclophosphamide, cisplatin; radiation exposure 5000 cGy assoc. increased risk of stricture
    • sxs: dysphagia, odynophagia
    • tx: supportive tx, dilation
  • corrosive: ingestion of alkali or acid from attempted suicide
    • tx: steroids
35
Q

Zenker diverticulum

A
  • older pts, outpouching of posterior pharyngeal wall above upper esophageal sphincter in area of weakness bw 2 parts of inf post constrictor, stores undigested food and pushes on lumen of esophagus
  • sxs: dysphagia, halitosis, regurg of undigested food, globus sensation, coughing after eating, wt loss, borborygmi in neck
  • dx: barium swallow, manometry
  • tx: requres only if sxatic cricophayngeus myotomy, no intervention if small (<2cm), botulinum toxin for temporary relief
  • complications: aspiration and PNA
36
Q

anorectal fistulas etiology and sxs

A
  • 10% associated with IBD, tuberculosis, malignancy, radiation
  • communication of abscess cavity with an identifiable internal opening within anal canal, most commonly located at dentate line where anal glands enter the canal
  • arise through obstruction of anal crypts or glands
    • intersphincteric (70%), transsphincteric, extrasphincteric, suprashpincteric
  • 40% are + for intestinal bacteria, male 2x > F, MCC = anorectal abscess
  • sxs: nonhealing anorectal abscess folowing drainage or chronic purulent drainage and pustule-like firm mass in perianal or buttock area, intermittent rectal pain (worse with defecation, sitting, and activity), malodorous perianal drainage, pruritus
  • signs: excoriation and inflammation of perianal skin, inflamed, tender, draining, external opening
37
Q

anorectal fistulas dx and tx

A
  • dx: all require anoscopy with diluted hydrogen peroxide to look for internal opening, imaging not required, drain with Mallenkot catheter, then fistulagram to search for an occult fistula tract, parks classification system
  • tx:
    • simple: fistulotomy with probing (preferred) - decreased risk of incontinence and recurrence, shorter healing time; simple ligation of internal fistula tract procedure, fistulectomy (larger wound, prolonged healing time, higher risk of incontinence
    • complex: seton (vessel loop r silk tie placed through fistula tract - reduces risk of incontinence in cases where poor would healing expected, can be initial temporary intervention or for complex fistulas who fail initial tx), can also do fistulotomy
38
Q

esophageal stricture

A
  • narrowing of esophageal lumen through inflammation, fibrosis, neoplasia, direct invasion or lymph node enlargement, disruption of peristalsis or lower esophageal sphincter function
  • causes: mostly sequelae of long-term GERD induced esophagitis (70-80%), originate at squamocolumnar jn
  • MC: old white men
  • sxs: heartburn, dysphagia (progressive with solid foods first and then liquids), odynophagia, food impaciton, wt loss, CP
    • atypical: chronic cough, asthma secondary to aspiration
  • dx: barium swallow, manometry, CT scan (staging), EGD - used to confirm, ro malig, bx and cytology, more sensitive than barium (edema, cellular infiltration, basal cell hyperplasia, inc type III collagen deposition), CXR
  • tx: mech dilation, lifestyle mods, wt loss, small meals, correct dentition, avoid NSAIDs/ASA
    • PPI > H2 blockers, 30% require repeat dilation in 1y
  • poor prognostic factors: lack of heart burn and significant wt loss
  • complications: bleeding, bacteremia
39
Q

diverticulosis

A
  • MOA: inc luminal pressure
  • RF: low fiber diet, + family hx, prevalence (inc age >60)
  • MC location = sigmoid colon
  • presence of diverticula - constipation leads to expulsion of diverticula in sigmoid colon
  • hx of constipation: asxsatic - discovered incidentally, only 20% sxatic (LLQ discomfort, bloating, constipation, diarrhea, lower GI bleed)
  • dx: KUB (ro free air), CT if pt doesnt respond to tx, barium enema - avoid during acute eps, leads to perforation and peritonitis, colonoscopy (avoid during acute eps)
  • tx: high-fiber diet (bran) to bulk up stool, psyllium
  • complicaitons: painless rectal bleeding with sudden-onset large volume hematochezia; spontaneously resolves - if continuous or recurrent go to surg, diverticulitis
40
Q

acute diverticulitis

A
  • defined as inflammation and/or infxn of diverticulum, feces impacted in diverticulum = erosion + microperf
  • mean age = 63; gram neg rods and anaerobes (E. coli, B. fragilis)
  • sxs: sudden onset abd pain in LLQ or suprapubic region (constant over several days, 50% w/ previous episode, N/V/C/D, +/- fever
  • signs: painful mass on rectal exam
  • dx: abd CT with contrast: localized bowel wall thickening (>4mm), increase soft tissue density in pericolonic fat, colonic diverticula, FOBT +, CBC (leukocytosis), avoid colonoscopy and barium enemas during acute eps
  • complications: diverticular abscess, colovesical fistula, bowel obst, perf
41
Q

treatment of diverticulitis

A
  • outpt: PO abx x7-10d (cipro + flagyl; bactrim + flagyl; augmentin)
    • consume clear liquids only until reassessed after 2-3d
    • repeat imaging not necessary if clinically improved
  • prophylaxis: do NOT need to avoid nuts, seeds, popcorn; high fiber diet
  • inpt:
    • uncomp: IVF (LR or NS), pain meds (morphine, tylenol, hydromorphone), NPO (bowel rest) or clear liquid diet; IV abx until abd pain resolves (3-5d) - PO abx x10-14d (flagyl PLUS: cefazolin, cefuroxime, ceftriaxone, cefotaxime, ciprofloxacin, levofloxacin; OR single-agent (ertapenem, piperacillin/tazobactam); repeat imaging (ro abscess, perf), after 6wk pt needs colonoscopy to ro colon CA
    • comp or recurrent sx: bowel resection
42
Q

esophageal cancer

A
  • SCC (AA M, upper thoracic and midthoracic esophagus)
    • RF: alc and smoking
  • adenocarcinoma (white M, distal 1/3 of esophagus/GE junction)
    • RF: GERD and Barrett’s esophagus
  • sxs: dysphagia (MC; solids first, then liquids), wt loss, anorexia, odynophagia (pain with swallowing - late finding), hematemesis, hoarseness, aspiration PNA, tracheoesophageal or bronchoesophageal fistula, CP
  • dx: barium swallow, upper endoscopy w/ bx and brush cytology (required), transesophageal US (depth), CT scan of chest/abd, CXR and bone scan
  • tx: palliative care, surg, chemotx with radiation
  • poor prognosis: 5y survival rate is 5-15% for both types
43
Q

gastric cancer

A
  • ulcerative carcinoma - ulcer through all layers
  • polypoid carcinoma - solid mass projects into stomach
  • superficial spreading - best prognosis
  • linitis plastic - through all layers, poor prognosis
  • most are adenocarcinomas - rare in US
  • RF: h. pylori infxn (3-6x), pernicious anemia (3x), severe atrophic gastritis, gastric dysplasia, adenomatous gastric polyps, post-antrectomy (15-20y), blood type A, high intake of preserved foods (high salt, nitrates, nitrites)
  • sxs: abd pain, unexplained wt loss, reduced appetite, anorexia, dyspepsia, early satiety, N/V, anemia, melena
  • signs: acanthosis nigricans
  • dx: FOBT, endoscopy with multiple bxs (most accurate), barium upper GI series, abd CT for staging
  • tx: surg resection with wide (>5cm margins): total or subtotal gastrectomy or extended lymph node dissection, chemo
44
Q

hepatocellular carcinoma etiology and sxs

A
  • >80% of primary liver cancers
  • MC type = non-fibrolamellar, associated with Hep B/C and cirrhosis, unresectable with short survival time
  • fibrolamellar - not associated with Hep B/C or cirrhosis, resectable, long survival time; seen in younger age
  • RF: cirrhosis (ETOH, hep b/C), chemical carcinogens, AAT def, hemochromatosis, Wilson’s dz, schiztosomiasis, hepatic adenoma, smoking, glycogen storage dz (type I)
  • sxs: abd pain (painful hepatomegaly), palpable liver mass, wt loss, anorexia, fatigue, signs/sxs of chronic liver dz - portal HTN, ascites, jaundice, paraneoplastic syndromes - high RBC/platelet, Ca, cholesterol (hypoglyc, carcinoid syndrome, pulm osteodystrophy)
45
Q

hepatocellular carcinoma dx and tx

A
  • dx: liver bx, Hep B and C serology, LFTs, coags, US< CT chest/abd/pelvis, MRI or MRA, A-1-FP tumor marker (high in 40-70% of pts)
  • tx: liver resection and/or liver transplant
  • survival/prognosis: if unresectable = less than 1y; if resectable = 25% 5y prognosis
46
Q

rectal cancer

A
  • 20-30% of all CRCs
  • sxs: hematochezia (most common), tenesmus (constantly feel like you have to go), rectal mass (feeling of incomplete evacuation of stool)
47
Q

celiac disease

A
  • autoimmune dz caused by transflutaminase abs after being exposed to gluten - reacts with small intestine causing villus atrophy
  • hypersensitivity to gluten caused by autoantibodies that attack tthe intestinal villi
  • sxs: diarrhea, wt loss, abd distention, bloating, infert in women
  • signs: dermatitis herpetiformis (vesicular rash found on extensor surfaces of arms and legs
  • dx: (+) anti-endomysial abs OR anti-transglutaminase abs, bx in proximal small bowel (villus atrophy and blunting in the small bowel), iron deficiency anemia (poor iron absorption), megaloblastic anemia (poor folic acid/B12 absorption)
  • tx: gluten free diet
  • prognosis: inc risk of cirrhosis
48
Q

cancer (esophagus, hepatic, stomach, gallbladder)

A
  • most common malignant liver trumors are hepatocellular carcinomas and cholangiocarcinomas
  • the most common benign liver tumor is the hemangioma
  • gastric cancer mets (VISK-shelf) superior to inferior
    • Virchow’s node - metastasis to the supraclavicular FOSSA NODES
    • Irish’s node - metastasis to LEFT AXILLARRY ADENOPATHY
    • Sister Mary Joseph’s node - metastasis to the periumbilical LYMPH NODE
    • Krukenberg’s tumor - metastasis to OVARY
    • Blumer’s SHELF - metastasis to the RECTUM (pelvic-cul-de-sac); palpable