Gastroenterology Flashcards

1
Q

6 big laboratory screen test for malabsorption

A
  1. Iron studies
  2. Prolonged PT
  3. Low calcium (vitamin D deficiency)
  4. Low cholesterol
  5. Low carotene
  6. Positive Sudan stain of the stool for fat (good screening test for steatorrhoea)
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2
Q

What food needs to be excluded in gluten-free diet?

A
  1. Wheat
  2. Rye
  3. Barley

Symptoms usually improve in weeks and histology in months if coeliacs disease is present

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3
Q

Extracolonic manifestations of Crohn’s disease

A
  1. Liver disease (PSC less common than UC)
  2. Gallstone disease (due to decreased bile salt pool)
  3. Renal disease due to urate and calcium oxalate stones, amyloidosis
  4. Malabsorption due to SB involvement
  5. Osteomalacia
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4
Q

What histological features are suggestive of UC over Crohn’s disease?

A

Mucus depletion and prominent crypt abscess

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5
Q

Bowel cancer screening in UC/Crohns

A

1-2 yearly screening if pancolitis for >7 years or L sided colitis for 15 years

If high grade dysplasia is seen in setting of severe inflammation, assessment of dysplasia can be misleading and should be repeated once Pt is stable.

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6
Q

Assessment of severity of UC

A

Mild - <4 bowel motions/day, minimal bleeding, normal pulse rate and temperature

Acute severe - >6 BM/day, profuse bleeding, temperature >37.5, HR >90, abdominal tenderness

Fulminant - >10 BM/day, continuous bleeding, fever and tachycardia, abdominal tenderness and distension

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7
Q

Sulfasalazine - SE, minimal dose

A

Mostly reaction to sulfapyridine - allergic reaction such as skin rash and SJS, haemolytic anaemia, nausea, headache, folate deficiency, reversible male infertility)

If reaction to sulfasalazine, use mesalazine which is the active component of sulfasalazine.

Minimum dose is 4g/day
Used indefinitely in UC to decrease relapse rate

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8
Q

Side effect of azathioprine/6MP

A
  1. Pancreatitis in 3%

2. Reversible bone marrow suppression

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9
Q

Manifestations of UC which are not cured by colectomy

A
  1. Ankylosing spondylitis
  2. Liver disease
  3. Pyoderma gangrenosum
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10
Q

Management of Crohn’s disease

A

Sulfasalazine/mesalazine - for colonic disease
Budesonide for SB disease esp ileocolonic disease
AZA/MTX are used to reduce long term relapse rates

With extensive ileal disease with bile salt diarrhoea, use Cholestyramine for bile salt sequestration

Metronidazole or ciprofloxacin is modestly useful in severe perianal disease and fistulaes - but tends to recur when stopped

TNF alpha inhibitor for fistulising disease

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11
Q

Causes of ascites based on SAAG >11g/L and <11g/L

A

> 11g/L - secondary to portal hypertension

  1. Cirrhosis
  2. Alcoholic hepatitis
  3. Cardiac ascites
  4. Budd Chiari syndrome (hepatic vein thrombosis) or IVC obstruction

<11g/L - not related to portal hypertension

  1. Peritoneal TB
  2. Peritoneal carcinomatosis
  3. Pancreatitis
  4. Nephrotic syndrome
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12
Q

Factors which can exacerbate acute hepatic encephalopathy in cirrhosis

A
  1. GIB
  2. Alkalosis - increases ammonia crossing BBB
  3. Hypokalaemia - causes increased renal ammonia production
  4. Infection
  5. Constipation
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13
Q

6 extrahepatic manifestations of HCV

A
  1. Mixed cryoglobulinaemia
  2. Porphyria cutanea tarda
  3. MPGN
  4. Hashimoto’s thyroiditis
  5. B cell lymphoma
  6. Polyarthralgia/polyarthritis
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14
Q

5 factors in Child Pugh score

A

3 serological factors which assess synthetic function (Bilirubin, INR, albumin)

2 Clinical factors (ascites, hepatic encephalopathy)

Max score of 15, with 1 year survival being:

5-6 = class A 100%
7-9 = class B 80%
10-15 = class C 45%
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15
Q

Distinguishing features of a spleen compared with a kidney

A
  1. Spleen has no palpable upper border
  2. Spleen has a notch
  3. Spleen moves inferomedially on respiration
  4. No resonance over a splenic mass
  5. Spleen is not bimanually palpable (ie not ballotable)
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16
Q

5 causes of MASSIVE hepatomegaly

A
  1. Metastasis
  2. Alcoholic liver disease with fatty infiltration
  3. Myeloproliferative disorder
  4. Right heart failure
  5. HCC
17
Q

6 causes of bilateral/unilateral renal masses

A
  1. Polycystic kidneys
  2. Hydronephrosis
  3. RCC
  4. Acute renal vein thrombosis
  5. Amyloid/infiltrative disease
18
Q

4 causes of massive splenomegaly

A
  1. CML
  2. Myelofibrosis
  3. Primary splenic lymphoma
  4. Hairy cell leukaemia
19
Q

5 causes of mild-moderate splenomegaly

A
  1. Infection (eg: infectious mononucleosis)
  2. CTD: eg RA, SLE
  3. Infiltrative disease such as amyloidosis and sarcoidosis
  4. Other myeloproliferative disorders such as PRV, ET
  5. Lymphoma
20
Q

6 causes of hepatosplenomegaly

A
  1. Chronic liver disease with portal hypertension
  2. Haematological disorders such as MPD, lymphoma, leukaemia
  3. Infection (acute viral hepatitis, glandular fever)
  4. Infiltrative disease such as sarcoidosis, amyloidosis
  5. CTD: SLE
  6. Acromegaly
21
Q

How will you manage this patient’s cirrhosis?

A

Mnemonic - PORTAL VEIN

Prognosis - CP score
Origin - ?HBV/HCV, specific therapy available
Rehab - eg: alcohol
Transplant - need to assess for appropriateness
Ascites - spironolactone, frusemide, salt restriction etc
Lifestyle - nutrition, multivitamins etc

Varices - non selective BB, banding
Encephalopathy - treat reversible factors, lactulose
Infection - vaccinate
Neoplasia - regular screening

22
Q

5 causes of R iliac fossa mass

A
  1. Caecal carcinoma
  2. Psoas abscess
  3. Pelvic kidney
  4. Ileocaecal tuberculosis
  5. Appendiceal abscess
23
Q

5 causes of L iliac fossa mass

A
  1. Faeces
  2. Sigmoid carcinoma
  3. Diverticular disease
  4. Ovarian tumour
  5. Psoas abscess
24
Q

Causes of upper abdominal mass

A
  1. Retroperitoneal lymphadenopathy
  2. Stomach cancer
  3. Pancreatic tumour/cyst
  4. Carcinoma of transverse colon