Gastro Flashcards

1
Q

Ulcerative Colitis extraintestinal ass

A

Primary sclerosing cholagitis

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2
Q

endoscopy findings in UC

A

ulceration with preservation of adj mucosa-> pseudopolyps

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3
Q

UC Mx- Mild to Mod

A

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

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4
Q

UC Mx- severe

A

> 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

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5
Q

Maintenance Mx for UC

A

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

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6
Q

LFT for AFLD & US findings

A

ALT> AST
increased echogenicity on US

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7
Q

Coeliac Disease associated disease + strongly ass with which immuno

A

dermatitis herpetiformis, DM1, autoimmune hepatitis

HLA-DQ2, HLA- DQ8

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8
Q

Dx Coeliac disease: serology + gold standard

A

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

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9
Q

How to calculate alcohol units

A

Volume ml x ABV (in decimal) divided by 1000

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10
Q

Haemochromatosis definition and genetic inheritance

A

AR disorder of iron absorption and metabolism

HFE gene on chromosome 6

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11
Q

Iron studies in haemochormatosis

A

Decreased TIBC, increased transferrin saturation M >55%, >50% F
Ferritin high later on

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12
Q

Mx haemochromatosis

A

1st line: gene section weekly monitor adequacy of venesection transferring saturation aim <50%, serum ferritin concentration <50yg/L

2nd line: deferrioxamine

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13
Q

LFT and mx alcoholic liver disease

A

High GGT
AST:ALT >2 , ratio >3 strongly suggests acute alcoholic hepatitis

Mx: glucocorticoids (prednisolone) often used in acute episodes of alcoholic hepatitis

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14
Q

Autoimmune hepatitis classification

A

Type I: ANA and SMA adult and children

Type II: LKM1 Ab children only

Type III: soluble liver kidney Ag adults middle age

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15
Q

Lab findings in Autoimmune hepatitis and other Ix

Mx

A

ANA/ SMA/ LKM1 Ab/ increased IgG

Liver biopsy: piecemeal necrosis, bridging necrosis

Steroid other immunosuppressants

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16
Q

Non-alcoholic fatty liver disease progression and LFT findings

A

Steatosis, stratohepatitis fat with inflammation, progressive disease- fibrosis and liver cirrhosis

LFT: ALT>AST

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17
Q

Inheritance of Wilson’s disease

A

Increased copper absorption and decreased copper excretion

AR, defect ATP7B gene on chromosome 13

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18
Q

Ix esp lab findings in `wilsons disease

A

Keyer -fleischer Ring

Decreased serum ceruloplasmin- carries cupper
Decreased total serum copper, free non-ceruloplasmin bound serum copper increased

Increased 24 hour Cu excretion

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19
Q

Mx Wilson’s disease

A

Penicillamine chelates Copper 1st line

Trentine hydrochloride alternate chelating agent may become 1st line in future. Tetrathiomolybolate newer agent

20
Q

Ass disease with primary biliary cholangitis

A

Sjogren 80%

RA, systemic sclerosis, thyroid disease

21
Q

Ix os primary biliary cholangitis

A

High ALP, aMA Ab- anti mitochondrial M2 Ab, high IgM
US and MRCP

22
Q

Mx of primary biliary cholangitis

A

1st line: ursodeoxycholic acid
Pruritus: chilestyramine
Liver transplant if Bb >100

23
Q

Relationship between primary sclerosing cholangitis and UC

A

UC 4% pts have PSC
PSC 80% pts have UC

24
Q

Ix of primary sclerosing cholangitis

A

WRCP/ MrCP std dx multiple biliary strictures beaded appearance

P-ANCA maybe +

25
PBC vs PSC
PBC- intrahepatic bile duct inflammation, AMA, ursodeoxycholic acid improves survival PSC- intra and extra hepatic bile duct inflammation Ass with UC, ursodeoxycholic acid does not improve survival
26
Mirrizi syndrome
Common hepatic duct obstruction caused by extrinsic compression from impacted stone in cystic duct/ infundibuoum of gall bladder
27
Ix and mx of bile acid malabsorption
SeHCAT: nuclear medicine test using gamma emitting molecule scan done 7d apart to assess retention/ loss of radiolabelled SeHCAT Mx: bile acid sequestration- cholestyramine
28
Most common cause of HCC world and Europe
World help B, Europe help C
29
Endoscopy findings of UC and CD
UC: widespread ulceration with preservation of adjacent mucosa which has appearance of polyps CD: deep u,cert skip lesions cobble stone like appearance
30
Classification of UC
Mild: <4 stools/day, small amount of blood Mod: 4-6 stools/day, varying amount of blood, no systemic upset Severe: >6 stools/day and feature of systemic upset.
31
Maintenance of left sided/ extensive UC and following severe relapse/ >2 exacerbation in post year
Left sided + extensive UC: low maintenance dose of po aminosalicylate Following severe relapse/ >2 exacerbation in past year:po azathioprine or po mercaptopurine.
32
Associated sx in CD and uC
CD and UC: arthritis, erythema nodosum, osteoporosis CD: episcleritis UC: pSC, uveitis
33
1st line for maintaining remission for CD
Azathioprine/ mercaptopurine
34
Associated disease in coeliac disease
Dermatitis herpetiformis, autoimmune disorder: type 1 DM, autoimmune hepatitis, HLA-DQ2 and HLA-DQ8
35
How long to you have to take gluten before dx of coeliac disease
6 weeks
36
H pylori dx
Urea breath test - may be used to check H pylori eradication Rapid urease test CLO test
37
Mx of Barrett’s oesophagus
High dose PPI Endoscopic surveillance with biopsies for metaplasia If dysplasia- 1st line radiofreq ablation esp for low grade dysplasia . Endoscopic mucosal resection
38
Which score to use in UGIB
Glasgow blatchford score OP/IP mx Rock all score
39
Peru’s jeghers syndrome inheritance
AD numerous polyps in HI tract Haemartomatous polyp in GI tract mainly SMALL bowel- SBO or intussusception and increased GI bleeding
40
Ix pancreatic cancer
CT investigation of choice
41
Ascites Ix
SAAG serum ascites albumin gradient >11g/L and <11g/L >11g/L: liver disorder are the most common cause- cirrhosis/ alcoholic liver disease, acute liver failure, liver metastases, cardiac rt heart failure, constrictive pericarditis, other causes- budd chairing syndrome, portal vein thrombosis, venom-occlusive disease, myxoedema] <11g/L: hypoalbuminaemia- nephrotic sy, severe malnutrition, malignancy , infection tuberculous peritonitis, other causes- pancreatitis, vowel obstruction, biliary ascites, postoperative lymphatic leak, serositis in connective tissue disease
42
Mx ascites
Fluid restrict is Na- <125mmol/l Aldosterone ATG spironolactone, albumin cover HAS, decreased paracentesis-induced circulatory dysfunction & mortality, paracentesis induced circulatory dysfunction Prophylactic abx
43
Virchow’s node, sister Mary Joseph node
Virchows node left supraclacivular LN Sister Mary Joseph’s Node
44
Pernicious anaemia Ix and ass disease
Ab to intrinsic factor +/- gastric parietal cells Ass disease: thyroid, DM1, addisons, RA, viltiligo
45
Ix carcinoid tumour
Urinary 5-HIAA Plasma choreographing A
46
Mx of carcinoid tumour
Somatostatin analogue Diarrhoea:cryproheptadine