Gastroenterology SMLE Review Notes

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Vocabulary-style flashcards based on Gastroenterology SMLE review notes covering esophageal, gastric, hepatic, and intestinal disorders.

Last updated 6:44 AM on 5/19/26
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26 Terms

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Dysphagia

Difficulty in swallowing, which can be caused by oropharyngeal neurological issues or esophageal lumen obstruction and motility disorders.

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Odynophagia

Pain during the act of swallowing.

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Heartburn

A condition where stomach contents are forced back up into the esophagus.

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Plummer-Vinson syndrome

A syndrome characterized by the triad of dysphagia, iron deficiency anemia (IDA), and an esophageal web.

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Diffuse esophageal spasm

A motility disorder presenting with chest pain relieved by Nitroglycerine or cold milk, showing a corkscrew appearance on barium swallow.

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Achalasia

An esophageal motility disorder characterized by dysphagia to solids and liquids, regurgitation of undigested food, and a bird beak appearance on barium swallow.

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Barrett’s esophagus

A pre-malignant condition where the normal squamous lining of the lower esophagus is replaced by columnar mucosa, potentially containing intestinal metaplasia.

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H. pylori Non-invasive tests

Diagnostic methods including Serology, Urea breath test, and Fecal antigen test.

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H. pylori Triple therapy

A treatment regimen consisting of a PPI, Clarithromycin, and either Amoxicillin or metronidazole for 1414 days.

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Bismuth quadruple therapy

A treatment regimen for H. pylori consisting of bismuth, Tetracycline, Metronidazole, and a PPI for 1414 days.

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Restrictive transfusion strategy

The practice of transfusing blood in UGIB only if Hb<7Hb < 7 (unless the patient has cardiac comorbidities where the target is higher).

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ALT/LDH ratio

A ratio used to differentiate AST/ALT elevations >1000> 1000; a ratio >1.5> 1.5 suggests viral hepatitis, while <1.5< 1.5 suggests drug-induced injury or liver ischemia.

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Wilson disease

A disorder of abnormal copper accumulation in the brain and liver, presenting with liver cirrhosis and neurological symptoms; treated with Penicillamine.

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Hereditary Hemochromatosis

A primary iron overload disorder screened via fasting serum transferrin saturation and confirmed by genetic testing.

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Non-alcoholic fatty liver disease (NAFLD)

Liver fat accumulation associated with obesity, insulin resistance, and type 22 DM; treated with weight loss and Vitamin E (for non-diabetics).

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Primary biliary cholangitis (PBC)

A female-predominant disease involving pruritis, high ALP, and positive anti-mitochondrial antibody (AMA).

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Primary sclerosing cholangitis (PSC)

A male-predominant disease associated with ulcerative colitis, characterized by pruritis, high ALP, and a string of beads appearance on MRCP.

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Serum Ascitic albumin gradient (SAAG)

Calculated as Serum Albumin - Ascitic Albumin; a value >1.1> 1.1 indicates causes like cirrhosis or cardiac ascites.

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Spontaneous Bacterial Peritonitis (SBP)

An infection of ascitic fluid confirmed by a granulocyte count >250> 250, treated with IV Cefotaxime or Ceftriaxone.

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Child-Pugh Classification

A scoring system for liver cirrhosis: Class A (well compensated, score 55 to 66), Class B (significant compromise, score 77 to 99), and Class C (decompensated, score 1010 to 1515).

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Celiac disease

An immune-mediated reaction to gluten (wheat, rye, barley) resulting in flat mucosa, villous atrophy, and crypt hyperplasia on jejunal biopsy.

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Dermatitis herpetiformis

An itchy, blistering skin rash that is a commonly associated diagnosis with celiac disease.

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Crohn disease

An inflammatory bowel disease characterized by transmural involvement, skip lesions, and non-caseating granulomas, commonly affecting the terminal ileum.

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Ulcerative colitis

An inflammatory bowel disease characterized by continuous distribution starting in the rectum, affecting the mucosa and submucosa, and presenting with bloody diarrhea.

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Rome 4 criteria

Diagnostic criteria for IBS requiring recurrent abdominal pain at least 11 day per week in the last 33 months related to defecation or change in stool frequency/form.

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