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28 Cards in this Set
- Front
- Back
Bacterial overgrowth |
Small bowel diverticulae B12 malabsorption - causes subacute cord degeneration Folate excess as bacteria synthesise folate |
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Small intestine dilation + oedema + fluid secretion which dilutes barium during its passage through small intestine |
Tropical sprue Coeliac disease Olmesartan-associated enteropathy Scleroderma Hypoalbuminemia Anasarca |
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Lymphocytic colitis |
One type of microscopic colitis. The other being collagenous colitis Can co-exist with other colitis Associated with long term NSAID, PPI, SSRI Lymphocytic infiltrate on colonic bx
Treatment: budesonide |
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Gardner's syndrome |
Autosomal dominant Multiple intestinal polyps Osteomas Soft tissue tumour (epidermoid cysts, fibromas, lipomas) |
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Hep B |
Compensated liver - first line: peginterferon - second line: tenofovir Decompensated liver - first line: tenofovir |
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Autoimmune hepatitis |
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Fatty liver of pregnancy Vs cholestatis of pregnancy |
Fatty liver is associated with constitutional symptoms |
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Bile acid malabsorption |
14C glycolate test Previous ileal resection |
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Calcification on AXR |
Hydatid disease Porcelain gallbladder |
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Whipple's disease |
Systemic disease caused by Tropheryma whippeli Middle-aged European white men Migratory arthralgia of large joints Arthritis Intermittent diarrhoea Colicky abdo pain CNS sx eg disinhibition Periodic acid Schiff (PAS) stain positive on jejunal bx 1yr cotrimoxizole/tetracycline |
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Budd chiari |
Think APLS Raised APTT but normal PT |
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UC |
pANCA Hypoalbuminaemia Crypt abscess |
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Achalasia |
Nifedipine/ISDN Botox |
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Coeliac disease |
Associated with T-cell lymphoma (raised viscosity) Anti-endomysial |
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PBC |
Middle aged women Itching AMA High ALP High IgM UDCA |
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Hydatid disease |
Echinococcus granulosis Percutaneous aspiration (PAIR procedure) Albendazole |
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Neuroendocrine tumour |
Carcinoid (ileum, appendix) Pancreatic endocrine tumour (different from exocrine tumour eg adenocarcinoma) |
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Carcinoid tumour |
Serotonin Substance P |
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Pancreatic endocrine tumour |
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CMV colitis |
Associated with UC treated with immunosuppressant Inclusion bodies on biopsy Treat with ganciclovir |
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Wilson's disease |
Trientene/penicillamine/zinc supplement ATP7B gene faulty - H1069Q mutation most common in Caucasian, whereas R778L is more common in China PRNP gene variant may delay onset |
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FMF |
Recurrent acute abdomen (normal laparotomy) Treatment: colchicine |
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Cowden syndrome (PTEN defect) |
Hamartomatous polyps Oral mucosal papilloma Palmoplantar keratosis Trichilemmomas Associated with breast and thyroid disorder |
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Schistosomiasis (Mansoni) |
Periportal fibrosis |
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Toxic megacolon |
IV ciclosporin |
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Colonoscopy interval for familial syndromes |
1 year - high risk patients (5 or more adenomas less than 10mm, or 3 or more adenomas larger than 10mm) 3 years - intermediate risk (3-4 adenomas less than 10mm, or 1-2 adenomas larger than 10mm) 5 years - low risk |
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FAP Vs HNPCC |
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Haemochromatosis |
Bronze diabetes Genetics HFE gene - C282Y mutation most common in white population, followed by H63D |