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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

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

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

Gardner's syndrome

Autosomal dominant


Multiple intestinal polyps


Osteomas


Soft tissue tumour (epidermoid cysts, fibromas, lipomas)

Hep B

Compensated liver


- first line: peginterferon


- second line: tenofovir



Decompensated liver


- first line: tenofovir

Autoimmune hepatitis

Fatty liver of pregnancy Vs cholestatis of pregnancy

Fatty liver is associated with constitutional symptoms

Bile acid malabsorption

14C glycolate test


Previous ileal resection

Calcification on AXR

Hydatid disease


Porcelain gallbladder

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

Budd chiari

Think APLS


Raised APTT but normal PT

UC

pANCA


Hypoalbuminaemia


Crypt abscess

Achalasia

Nifedipine/ISDN


Botox

Coeliac disease

Associated with T-cell lymphoma (raised viscosity)


Anti-endomysial

PBC

Middle aged women


Itching



AMA


High ALP


High IgM



UDCA

Hydatid disease

Echinococcus granulosis



Percutaneous aspiration (PAIR procedure)


Albendazole

Neuroendocrine tumour

Carcinoid (ileum, appendix)


Pancreatic endocrine tumour (different from exocrine tumour eg adenocarcinoma)


Carcinoid tumour

Serotonin


Substance P



Pancreatic endocrine tumour

CMV colitis

Associated with UC treated with immunosuppressant


Inclusion bodies on biopsy


Treat with ganciclovir

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

FMF

Recurrent acute abdomen (normal laparotomy)


Treatment: colchicine

Cowden syndrome (PTEN defect)

Hamartomatous polyps


Oral mucosal papilloma


Palmoplantar keratosis


Trichilemmomas



Associated with breast and thyroid disorder

Schistosomiasis (Mansoni)

Periportal fibrosis

Toxic megacolon

IV ciclosporin

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

FAP Vs HNPCC

Haemochromatosis

Bronze diabetes



Genetics


HFE gene - C282Y mutation most common in white population, followed by H63D