GP Gastrology Flashcards

1
Q

A 35 year old woman presents with jaundice, RUQ pain and pruitis: whats this presentation typical of?

A

Primary Sclerosing Cholangitis

biliary disease of unknown aetilogy causing inflammation and sclerosis of the biliary tree.

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2
Q

What is the most common association for patients with PSC to have?

A

80% of patients with PSC have Ulcerative colitis

**additional risk of complication of cholangiocarcinoma

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3
Q

What are the appropriate blood tests to order to confirm/rule out a diagnosis of coeliac?

A
  • Tissue transglutaminase (TTG) antibodies
  • Endomyseal (EMAs) antibody
    • both IgA
    • **however some patients are severely IgA deficient
  • anti-casein antibodies are also found in some patients
  • anti-gliadin antibody tests NOT recommended by NICE
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4
Q

Who is most vulnerable to develop Spontaneous bacterial Peritonitis?

A

Patients with ascites.

Most commonly due to liver cirrhosis

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5
Q

When is it indicated to give prophylactic antibodies against spontaneous bacterial peritonitis?

**and what antibiotics do you use?

A

When the patient has ascites

+ a protien conc <15 g/L or

+ a previous episode of SBP or

+ child pugh score of 9 or more

They should be given ciprofloxacin or norfloxacin prophylactically

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6
Q

What tests do you need to make a diagnosis of spontaneous bacterial peritonitis?

A
  • Paracentesis of the ascitic fluid with show
    • Neutrophil cound >250 cells u/l
    • Positive organism culture (usually E.coli)
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7
Q

What should you look for on abdominal xray to confirm toxic megacolon?

A
  • Transverse Colon >6cm
  • Additional signs of systemic upset
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8
Q

Which of iron, folate and B12 are those with coeliac disease deficient in?

A

All three.

This is because coeliacs causes villous atrophy in all regions of the bowel (although maximum impact is seen in the duodenum)

  • B12: absorbed in the terminal ileum
  • Folate: in the duodenum and jejunum
  • Iron: mainly in the duodenum
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9
Q

What HLA strands are associated with coeliacs?

A

HLA-DQ2 and HLA-DQ8

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10
Q

What conditions are associated with coeliacs disease?

A
  • Autoimmune thyroid disease
  • Dermatitis Herpetiformis
  • Irritable Bowel Syndrome
  • Type 1 Diabetes
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11
Q

What are the three types of bowel ischaemia thatcan occur?

A
  • Acute Mesenteric Ischaemia: sudden, acute, impacts small bowel (typically due to an embolis)
  • Chronic Mesenteric Ischaemia: uncommon, thought of as ‘intestinal angina’
  • Ischaemic colitis: acute but transient, affects the small bowel.
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12
Q

What vessel is usually impacted in acute mesenteric ischaemia and what is the treatment?

A

The superior mesenteric artery

Tx is surgery, however prognosis is often poor if surgery is delayed.

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13
Q

What vessels are more likely to be impacted in ischaemic colitis?

A

More common in the watershed ares such as the splenic flextures

  • located at the borders of the territory supplied by the superior and inferior mesenteric arteries.
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14
Q

how to diagnose ischaemic colitits?

A
  • Thumbprinting can be seen on abdominal xray due to mucosal heamorrhage/oedema
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15
Q

Raised transferrin saturation and ferritin, with low TIBC

This is a characteristic blood result of what disease and why do we get these results?

A

Haemachromatosis

this is a condition which produces increased iron, leading to increasingly saturated transferrin and raised ferritin.

As ‘TIBC’ refers to total iron binding capacity on transferrin binding sites, this is actually decreased.

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16
Q

Haemachromotosis is caused by a gene mutation of the ____ gene.

On xray joints will show evidence of _______

A

Haemachromotosis is caused by a gene mutation of the HFE gene.

On xray joints will show evidence of chondrocalcinosis

17
Q

What investigations will help diagnose Chrohns disease?

A
  • Faecal calceprotein
  • Raised inflammatory markers
  • Anaemia
  • Low B12 and vitamin D
18
Q

What is it called when you have a sweet, faecal breath, and what is this an indicative of?

A

Fetor Hepaticus: this is indicative of liver failure

a late sign of hepatic encephalopathy

19
Q

Features of Wilsons Disease

A

Liver: hepatitis, cirrhosis

Neurological: basal ganglia degeneration, speech, behavioural and psychiatric problems

asterixis, chorea, dementia

Kayser Fleischer rings

Renal Tubular Acidosis

Haemolysis

Blue Nails

20
Q

What tests could prove a diagnnosis of Wilsons Disease

A

Reduced serum caeruloplasmin

Reduced Serum copper (counter-intuitive, but 95% of plasma copper is carried by caeruloplasmin)

Increased 24-hour urinary copper excretion

21
Q

Really high amylase is an indication of…..

A

Pancreatitis!

Think of the anagram GET SMASHED

22
Q

Intestinal angina is also know as what?

What is the classical triad seen in this disease?

A

Also known as Chronic Mesenteric Ischaemia

Triad of:

  1. Severe, colicky, post-prandial pain
  2. Weight loss
  3. Abdominal bruit

However this pathology can also be relatively non-specific!
Usually results from long-standing atherosclerotic disease of 2 or more mesenteric vessels

23
Q

Associations with Helicoabctor Pylori?

A
  • Peptic Ulcer Disease: Duodenal and gastric
  • Gastric Cancer
  • B cell thyomas of MALT tissue (80% regression with treatment)
  • Atrophic Gastritis
24
Q

Management of H. Pylori?

A

Triple Therapy of

PPI + amoxicillin + clarithromycin OR

PPI + metronidazole + clarithromycin

***statins and clarithromycin don’t mix!

25
Q

How to diagnose for H. Pylori involvement?

A
  • Stool antigen test or
  • Carbon-13 urea breath test. (Recommended to confirm eradication)
26
Q
A