Gastro Flashcards

1
Q

Crohns vs UC?

A

Crohns: non-bloody diarrhoea, abdominal pain (often right-sided), weight loss, and extraintestinal manifestations like oral ulcers or skin lesions; pei-anal disease eg skin tags, goblet cells

—> Tranny (transmural inflammation) granny (granulomas) skips (skip lesions) down the cobblestone (cobblestone appearance) alley

UC: Tender LLQ, bloody diarrhoea, abdominal pain, and a feeling of incomplete evacuation after defecation (tenesmus), urgency. Crypt abscess, psuedopolyps, colorectal ca

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2
Q

At what ages and how often are FITs done as part of the colorectal screening programme?

A

Faecal immunochemical tests are sent every 2 years to all patients aged 60-74 years in England, 50-74 years in Scotland.

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2
Q

Management of UC flare? severe vs mild-mod

A

definition of severe UC: >6 bloody stools per day + features of systemic upset (pyrexia, tachycardia, anaemia, raised inflammatory markers)

In mild/moderate: topical (rectal) aminosalicylate. –> PO aminosalicylate (eg Sulfasalazine)–> steroid

Severe: hospital. IV steroids –> IV ciclosporin –> surgery

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3
Q

What is pyoderma gangrenosum?

A

Inflammatory, not infection. An uncommon cause of very painful skin ulceration.
Associated with IBD.
Starts as pustule then ulcerates
Treat with steroids

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4
Q

WHat is used for prevenetion of variceal high risk bleeds?

A

A non-cardioselective B-blocker (NSBB) is used for the prophylaxis of oesophageal bleeding eg carvedilol, propranolol

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5
Q

Spider naevi vs telangiectasia

A

Spider naevi can be differentiated from telangiectasia by pressing on them and watching them fill. Spider naevi fill from the centre, telangiectasia from the edge

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6
Q

Mx of crohns flare up?

A

Induce remission:
1st line - steroids
2nd line - 5-ASA (aminosalicylaes) eg mesalazine
3rd line - azathioprine/ mercaptopurine /methotrexte.
4th line - infliximab
Metronidazole is used if fistula present

Maintain remission:
1st line - azathioprine/ mercaptopurine - need to test TPMT
2nd line - methotrexate

Surgery:
ileocoecal resection if stricture, resections, draining seton

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7
Q

How is SBP diagnosed?

A

In suspected SBP- diagnosis is by paracentesis. Confirmed by neutrophil count >250 cells/ul

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8
Q

How do you interpret Hep B serology?

A

HBsAg normally implies acute disease (present for 1-6 months)

if HBsAg is present for > 6 months then this implieschronic disease(i.e. Infective)

Anti-HBs implies immunity (either exposure or immunisation). It is negative in chronic disease.

Anti-HBc implies previous (or current) infection. IgM anti-HBc appears during acute or recent hepatitis B infection and is present for about 6 months. IgG anti-HBc persists.

HbeAg results from breakdown of core antigen from infected liver cells as is, therefore, a marker of infectivity. Marker of HBV replication and infectivity

Example results

previous immunisation: anti-HBs positive, all others negative

previous hepatitis B (> 6 months ago), not a carrier: anti-HBc positive, HBsAg negative

previous hepatitis B, now a carrier: anti-HBc positive, HBsAg positive

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9
Q

Achalasia vs oeseophgeal stricture vs pharyngeal pouch??

A

Achalasia - relaxed lower sphincter. Progressive dysphagia of solids and liquids on onset. Get CP, wt loss, reflux.
Bird beak sign on barium swallow

Oesophageal stricture - Presents with difficulty swallowing solids then liquids.
Narrowing on barium swallow
Often due to GORD and so will hve hx of reflux

Pharyngeal pouch - intermittent dysphagia halitosis + nocturnal coughing

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10
Q

Consequences of low vitamins:
A (Retinoids)
B3 (niacin)
c (Ascorbic acid)

A

A- night blindness
B3- Pellagra- dermatitis, diarrhoea, dementia
C- scurvy - gingivitis and bleeding

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11
Q

Describe autoimmune hepatitis - bloods/ presentation/ ix?

A

may present with signs of chronic liver disease
acute hepatitis: fever, jaundice etc (only 25% present in this way)
amenorrhoea (common)
ANA/SMA/LKM1 antibodies, raised IgG levels
liver biopsy: inflammation extending beyond limiting plate ‘piecemeal necrosis’, bridging necrosis

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12
Q

What is charcots triad? WHich condition does it occur in?

A

ascending cholangitis triad: fever, jaundice and right upper quadrant pain

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13
Q

Which ulcer is relived by eating?

A

duodenal

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14
Q

When should prophylactic abx be started for ascites? which abx?

A

Patients with ascites and protein concentration <= 15 g/L / Child-Pugh score of at least 9/ hepatorenal syndrome

they should be given oral ciprofloxacin or norfloxacin as prophylaxis against spontaneous bacterial peritonitis

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15
Q

What blds do you do to monitor response to haemochromatosis mx?

A

Ferritin and transferrin saturation (most useful also for diagnosis) are used to monitor treatment in haemochromatosis (venesection)

16
Q

What extra-intestinal manifestation of IBD colerates to flare ups?

A

erythema nodosum

17
Q

Describe primary biliary cholangitis?

A

Classically seen in middle aged women
Present with jaundice, raised ALP, pruritius

AMA - anti-mitochondrial antibodies highly specific (98%), raised IgM
Associated with sjogrens (80%)

first-line: ursodeoxycholic acid
cholestyramine if itchy, fat soluble vitamins, eventually liver transplant
Associated with HCC

18
Q

What should be given before OGD in UGIB?

A

Terlipressin and prophylactic abx

Post UGIB if NOT variceal bleed eg if ulcer give PPI

19
Q

Where is biopsy taken from to prove diagnosis of coeliacs?

A

Jejunum

20
Q

How do you test for h pylori?

A

Urea breath test
should not be performed within 4 weeks of abx or within 2 weeks of ppi/ h2 antag

21
Q

What condition is Melanosis coli found on biopsy of colon?

A

chronic use or abuse of anthraquinone-containing laxatives, such as senna or cascara.

22
Q

Curlings vs cushings ulcer?

A

Curling’s ulcer is a recognised complication of severe burns. It is a gastric ulcer caused by necrosis of the gastric mucosa, usually due to hypovolaemia. They carry a high rate of bleeding and mortality.

A Cushing’s ulcer is a stress ulcer that occurs in the aftermath of severe head trauma.

23
Q

What is the most commonly effected site in ulcerative colitis?

A

Ulcerative colitis - the rectum is the most common site affected

24
Q

What cancer does barretts put you at risk of vs achalasia?

A

Whilst Barrett’s oesophagus increases the risk of oesophageal adenocarcinoma, achalasia increases the risk of squamous cell carcinoma of the oesophagus.

25
Q

What is Peutz-Jeghers syndrome?

A

autosomal dominant condition characterised by numerous hamartomatous polyps in the gastrointestinal tract. It is also associated with pigmented freckles on the lips, face, palms and soles

26
Q

Treatment for wilsons disease?

A

penicillamine

27
Q

What cancer is coeliacs associated with

A

Coeliac disease increases the risk of developing enteropathy-associated T cell lymphoma of SI

28
Q

When should PO and rectal 5ASA be started for UC?

A

In a mild-moderate flare of ulcerative colitis extending past the left-sided colon, oral aminosalicylates should be added to rectal aminosalicylates, as enemas only reach so far

29
Q

How to maintain remission in UC?

A

Following a mild-to-moderate ulcerative colitis flare
proctitis and proctosigmoiditis
topical (rectal) aminosalicylate alone (daily or intermittent) or
an oral aminosalicylate plus a topical (rectal) aminosalicylate (daily or intermittent) or
an oral aminosalicylate by itself: this may not be effective as the other two options
left-sided and extensive ulcerative colitis
low maintenance dose of an oral aminosalicylate

Following a severe relapse or >=2 exacerbations in the past year
oral azathioprine or oral mercaptopurine