PREMIDTERM Flashcards

1
Q

imaging for esophagus

A

-oropharyngeal dysphagia- video esophagraphy
-EGD- GERD, infectious esophagitis -> rule out cancer in zenkers
-barium- dysphagia -> webs, rings, zenkers
-esophageal manometry- DES, achalasia
-esophageal pH recording
-U/S- tumors

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2
Q

GERD

A

-hiatal hernia
-gastroparesis obstruction
-LES abnormal
-EGD, barium, pH if nothing is working
-wt loss most helpful tx
-promotility agents
-step up vs step down approach
-PPI- long term use -> Ca and iron deficiency and epithelial polyps
-surgical fundoplication
-COMPLICATIONS- barrets, stricture (lower), Schatzki ring
-balloon dilate GERD stricture

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3
Q

esophagus things to biopsy

A

-eosinophilic esophagitis
-GERD stricture
-tumors
-infectious esophagitis

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4
Q

esophagus things with structures

A

-GERD
-eosinophilic esophagitis
-pill induced esophagitis
-caustic injury
-esophageal diverticula can be secondary to structure

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5
Q

barretts esophagus

A

-caused by GERD
-increased esophageal adenocarcinoma risk
-columnar epithelium lining
-EGD every 3-5 years with PPI -> normal switch to H2

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6
Q

eosinophilic esophagitis

A

-MC in younger
-genetic
-food allergy response -> high IgE
-EGD and barium
-concentric rings, vertical furrowing, white papules
-bx
-tx- eliminate milk, wheat, soy, nuts, fish, eggs
-dilate CAREFULLY
-inhaled steroids swallowed (fluticasone and PPI) -> dupixent if fail

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7
Q

caustic injury esophagitis

A

-CXR and abd x ray for perforation (pill esophagitis too)
-fluids
-EGD within 25 hrs
-if severe- high risk perf, TE fistula, bleeding, stricture -> surgery / feeding tube
-stricture!
-squamous cell carcinoma -> monitor after 15-20 years

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8
Q

esophageal webs

A

-upper esophagus (schatzki at bottom)
-congenital
-assoc with blistering skin ds- phemphigoid, epidermolysis bullosa, iron deficiency anemia
-plummer vinson syndrome (PVS)- dysphasia, web, iron deficiency

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9
Q

upper vs lower esophagus

A

-upper - zenkers?, webs, CMV
-lower- schatzki, herpes, cancer, achalasia

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10
Q

zenker diverticulum

A

-< 1cm no tx
->1cm or symptomatic -> surgcial or endoscopy tx
-aspiration, pneumonia, lung abscess, bronchiectasis

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11
Q

benign esophageal tumors

A

-lieomyoma MC
-large
-ulceration or pain
-EDG bx or barium
-need EUS to confirm benign

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12
Q

esophageal varices

A

-hematemesis, melena, hematochezia
-NG tube confirms UGI bleed
-FFP and platelets if coagulopathy
-EGD once stable
-tx- banding or sclerotherapy
-antibiotics if peritonitits
-vitamin K if abnormal PT
-lactulose if encephalopathic
-balloon tamponade and intubation if uncontrolled bleed
-TIPS
-beta blockers and banding for prevention
-liver transplant- >14 MELD
-EGD monitor with cirrhosis 1-3 years

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13
Q

esophageal cancer

A

-squamous cell -> achalasia, caustic induced stricture
-adenocarcinoma -> barretts
-TE fistula
-hoarseness
-high aminotransferase or alkaline phosphatease
-hypoalbuminemia

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14
Q

achalasia

A

-barium
-EGD- r/o cancer, stricture
-esophageal manometry
-aperistalsis distally
-esophagus pressure > gastric
-balloon dilation
-laproscopic myotomy
-cardiomyotomy of LES
-fundoplication
-botox

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15
Q

diffuse esophageal spasm

A

-DES
-non propulsive
-non coordinated
-tx- anticholinergics, ca channel blockers, nitrates
-sometimes chronic

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16
Q

erosive and hemorrhagic gastritis

A

-NSAIDs*(gastric), EtOH, stress, portal hypertension, caustic, radiation
-ASA aspirin is the worst
-EGD (not always necessary) -> subepithelial hemorrhages, petechiae, erosion
-concerns - anemia
-beta blockers for portal hypertension -> PPI for the rest
-+/- heme positive stool

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17
Q

H. pylori

A

-PUD -> more associated with duodenal
-gastric adenocarcinoma risk
-low grade B cell gastric lymphoma risk
-fecal antigen and urea breath tests
-EGD with bx - gold standard
-PPI (8 weeks gastric and 4 duodenal) + clarithromycin + amoxicillin ALL 2X DAY for 14 days
-can confirm its gone with stool or breath test -> must confirm gastric ulcer is gone with EGD

18
Q

pernicious anemia

A

-gland atrophy -> metaplasia -> cancer risk
-adenocarcinoma!!!
-parietal cell and intrinsic Ab
-high gastrin but low pH
-tx b12 injection
-pH > 3 -> hypochlorhydria

19
Q

PUD

A

-+/- heme positive stool
-+/- anemia
-high gastrin with ZE
-penetration/perforation - leukocytosis and increased amylase (if penetrating pancreas)
-bx for h pylori and cancer until healed -> EGD FU
-50% of UGI bleeds

20
Q

Zollinger-ellison syndrome

A

-pancreas, duodenal wall, or lymph node
-within the triangle -> porta hepatis, neck of pancreas, and 3rd portion of duodenum
-2/3 malignant
-metastases to liver
-leads to PUD, GERD
-ulcers + diarrhea, steatorrhea -> ZE
-duodenal ulcers usually solitary
-gastric ulcers are usually multiple
-gastrin tested in people with giant ulcers, neg h pylori, multiple duodenal ulcers, diarrhea, reoccurrences
-somatostatin receptor scintigraphy -> EUS
-PPI and resection

21
Q

gastric outlet syndrome

A

-pyloric outlet obstruction from inflammation
-rare
-vomiting*
-get full easily
-NG aspiration is smelly
-gastric emptying study
-NG decompression
-IV PPI
-EGD after

22
Q

stomach tumors

A

-usually benign
-epithelial polyps can be caused by long term PPI
-premalignant potential -> excision
-adenocarcinoma (MC) and lymphoma are malignant
-adenocarcinoma- polypoid, fungating, ulcerating* -> H. pylori and pernicious anemia high risk
-virchow node (supraclavicular), sister mary joseph (umbilical), blumers shelf (peritoneal), krukenberg (ovarian)
-failed PPI
-EGD, CT
-gastric lymphoma- MC non hodgkins B cell lymphoma (nodal) -> night sweats absent

23
Q

upper GI bleed

A

-PUD- 50%
-portal HTN- 10-20%
-mallory-weiss- 5-10%
-vascular ectasis- 7%
-neoplasm 1%
-erosive gastritis- chronic bleed
-NG tube- cant rule out duodenal source
-FFP and platelets if coagulopathy
-TIPS
-IV PPI
-cautery, infection, endoclips, octreotide, EGD after

24
Q

conjugated vs unconjugated

A

unconjugated:
-hemolysis
-genetic disease
-drug reaction
-stool and urine is normal

conjugated
-hepatocellular dysfunction
-biliary obstruction
-urine dark and stool light

25
acute hepatitis
-prodromal phase- tired, aches, anorexia, N/V, diarrhea, constipation, RUQ/epigastric pain -icteric phase- jaundice 5-10 days after -convalescent phase- recover -lymphadenopathy -hepatomegaly -PT prolonged, WBC low, AST/ALT high -2-3 weeks course -give vaccine as treatment (A+B) -FAILURE- encephalopathy in 8 weeks (fulminant) or between 8weeks-9months (subfulimnant) -> liver transplant, antiviral for HBV -MC cause of failure- acetaminophen toxicity (NAC), parvovirus B19
26
Hepatitis A
-RNA -fecal oral -Anti HAV IgM and IgG -vaccinate
27
hepatitis B
-DNA -sexual, blood, vertical transmission -1-5 months incubation long* -higher chance of chronic when young -vaccinate -HBsAg => actively infected, carrier state -Anti-HBs => vaccine OR prior infection -Anti-HBc- fills serologic gap -IgM anti-HBc => acute infection -IgG anti-HBc => chronic infection OR prior infection -HBcAg => not in the serum -HBeAg => active infection, >3 months likely to be chronic, infectivity and replication -HBV DNA => dormant in liver
28
hepatitis D
-RNA -D needs B to survive -percutaneous -does not increase probability of chronic B but it does make it worse
29
hepatitis C
-RNA -blood, body piercing, hemodialysis, tattoo -asymptomatic usually -> high chronic risk -Anti HCV- DOES NOT MEAN RECOVERY -> MEANS YOU HAVE BEEN EXPOSED -HCV RNA PCR- always order to see if still infected -ALT is not a marker- variable -no vaccine!
30
hepatitis E
-RNA -waterborne -self limited and NO CARRIER STATE* -high mortality in pregnant women
31
hepatitis G
-RNA -percutaneous -needle
32
decompensated cirrhosis
-jaundice -splenomegaly -ascites -> diuretics -peripheral edema -encephalopathy -liver flap -portal HTN* -fibrosis maybe -high alk phos, low albumin, prolonged PT, anemia, thrombocytopenia -monitor for HCC (US), LFTs, AFP every 6 months, EGD -MC cause of cirrhosis- chronic Hep C, alcohol, NASH -cirrhosis classified histologically -US and biopsy
33
chronic HBV
-extrahepatic complications- polyarteritis nodosa (inflammation of medium sized vessels) and glomerular disease -symptoms range from asymptomatic to failure -HBsAg > 6 months -> chronic -tx- nucleoside or pegylated interferon
34
chronic hep C
-fatigue and sleep disturbances MC -jaundice rare -hematologic disease -renal disease -diabetes mellitus -autoimmune disorders -dermatologic
35
autoimmune hepatitis
-autoantibodies and high serum globulim concentration -can follow viral illness -asymptomatic to hepatic failure -high ANA and ASMA -high bili, AST/ALT -liver bx -tx- prednisone +/- azathioprine -if cirrhosis monitor
36
primary biliary cholangitis
-rare -intrahepatic bile duct obstruction (small) -autoimmune -> environmental trigger -female -high LFTs -pruritis -high alk phos* -high AMA* -MRCP -tx- Ursodeoxycholic acid + Replacement of fat-soluble vitamins if deficient -monitor if cirrhosis
37
primary sclerosing cholangitis
-intra and estrahepatic bile duct obstructions -larger -> stent -males -assoc with IBD
38
hemochromatosis
-symptomatic at later age -heart failure, arrhythmias, type 2 diabetes, BRONZE SKIN -can develop HCC -high ferritin, iron, transferin -HFE gene mutation and high iron -> phlebotomy
39
alcoholic liver disease
-MC cause of cirrhosis -reversible -R/O other causes of liver disease first -steatosis (fat deposition in liver) or steatohepatitis (irritation due to fat in liver) -hepatomegaly -liver failure symptoms -AST>ALT -US/CT/MRI- shows steatosis, ascites, cirrhosis -bx not necessary
40
nonalcoholic fatty liver disease
-NAFL- fatty liver- normal labs -NASH- steatohepatitis -> vitamin E -MC liver disorder! -obesity, diabetes -> high risk -tx- steroids -ALT>AST -r/o other causes -imaging or bx required -> steatosis -NASH -> HCC**
41
staging of HCC
-bilirubin -albumin -PT time -ascites -encephalopathy