Gastro Flashcards
Ulcerative Colitis extraintestinal ass
Primary sclerosing cholagitis
endoscopy findings in UC
ulceration with preservation of adj mucosa-> pseudopolyps
UC Mx- Mild to Mod
Mild: <4stool day, only small amount of blood
Mod: 4-6 stool/day, varying amountof blood, no systemic upset
topical/ rectal aminosalicylate -> add po aminosalicylate -> po or topical corticosteroid
UC Mx- severe
> 6 blood stool/day + systemic upset
admit in hospital
iv steroid!! 1st line
iv ciclosporin if steroid CI OR add if no improvement after 72hrs
Maintenance Mx for UC
mild-mod:
proctitis topical aminosalicylate OR po aminosalicylate + rectal aminosalicylate
extensive UC: low maintenance dose po aminosalicylate
severe relap or >2 exacerbation: po azithioprine OR po mercaptopurine
LFT for AFLD & US findings
ALT> AST
increased echogenicity on US
Coeliac Disease associated disease + strongly ass with which immuno
dermatitis herpetiformis, DM1, autoimmune hepatitis
HLA-DQ2, HLA- DQ8
Dx Coeliac disease: serology + gold standard
need to take gluten for at lest 6 weeks
Serology: TTG-Ab IGA 1st line, Eendmyseal Ab IgA, Anti-gliadin, anti-casein Ab
Endoscopic intestinal biopsy=> GOLD STD traditionally taken from duodenum
Histo: villous atrophy, crypt hyperplasia, increased intraepithelial lymphocytes, laminia propria infiltration with lymphocytes
How to calculate alcohol units
Volume ml x ABV (in decimal) divided by 1000
Haemochromatosis definition and genetic inheritance
AR disorder of iron absorption and metabolism
HFE gene on chromosome 6
Iron studies in haemochormatosis
Decreased TIBC, increased transferrin saturation M >55%, >50% F
Ferritin high later on
Mx haemochromatosis
1st line: gene section weekly monitor adequacy of venesection transferring saturation aim <50%, serum ferritin concentration <50yg/L
2nd line: deferrioxamine
LFT and mx alcoholic liver disease
High GGT
AST:ALT >2 , ratio >3 strongly suggests acute alcoholic hepatitis
Mx: glucocorticoids (prednisolone) often used in acute episodes of alcoholic hepatitis
Autoimmune hepatitis classification
Type I: ANA and SMA adult and children
Type II: LKM1 Ab children only
Type III: soluble liver kidney Ag adults middle age
Lab findings in Autoimmune hepatitis and other Ix
Mx
ANA/ SMA/ LKM1 Ab/ increased IgG
Liver biopsy: piecemeal necrosis, bridging necrosis
Steroid other immunosuppressants
Non-alcoholic fatty liver disease progression and LFT findings
Steatosis, stratohepatitis fat with inflammation, progressive disease- fibrosis and liver cirrhosis
LFT: ALT>AST
Inheritance of Wilson’s disease
Increased copper absorption and decreased copper excretion
AR, defect ATP7B gene on chromosome 13
Ix esp lab findings in `wilsons disease
Keyer -fleischer Ring
Decreased serum ceruloplasmin- carries cupper
Decreased total serum copper, free non-ceruloplasmin bound serum copper increased
Increased 24 hour Cu excretion
Mx Wilson’s disease
Penicillamine chelates Copper 1st line
Trentine hydrochloride alternate chelating agent may become 1st line in future. Tetrathiomolybolate newer agent
Ass disease with primary biliary cholangitis
Sjogren 80%
RA, systemic sclerosis, thyroid disease
Ix os primary biliary cholangitis
High ALP, aMA Ab- anti mitochondrial M2 Ab, high IgM
US and MRCP
Mx of primary biliary cholangitis
1st line: ursodeoxycholic acid
Pruritus: chilestyramine
Liver transplant if Bb >100
Relationship between primary sclerosing cholangitis and UC
UC 4% pts have PSC
PSC 80% pts have UC
Ix of primary sclerosing cholangitis
WRCP/ MrCP std dx multiple biliary strictures beaded appearance
P-ANCA maybe +