Random revision Flashcards

1
Q

Achalasia - definition and pathogenesis

A

Loss of oesophageal peristalsis due to failure of relaxation of the lower oesophageal sphincter due to degeneration of the ganglionic nerve cells of the myenteric plexus

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2
Q

Achalasia - investigation findings and management

A
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3
Q

Coeliac disease - investigations and management

A

Bloods - remember to screen for deficiencies, so vitamins, calcium and phosphate, iron and folate, U&E and albumin
FBC would should low haemoglobin

Serology - anti-TTG IgA and esp IgG as IgA deficiency is common

Stool culture to exclude infection

Endoscopic biopsy - villous atrophy and crypt hyperplasia

Management - remove gluten + replace vitamins iron and folate, consider steroids of gluten free diet does not help

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4
Q

Key signs of coeliac disease

A

Dermatitis herpetiformis
Short stature/muscle wasting as a result of malnutrition

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5
Q

Colonic polyps - definition and how would you classify

A

Outpouching of normally flat mucosa

Split into neoplastic and non-neoplastic

Non-neoplastic can be due:
Inflammatory pseudopolyp - IBD
Harmatomatous polyp - syndromes
Hyperplastic polyps- post H pylori

Also: FAP due to APC gene

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6
Q

Colonic polyps - symptoms and management

A

Usually asymptomatic, but can present with PR bleeding if near rectum

Management - colonoscopic polypectomy

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7
Q

Which bile duct condition is associated with UC and what’s the definition + symptoms

A

Primary sclerosing cholangitis - fibrosis of the INTRahepatic and EXTRAhepatic bile ducts, hence why you get liver disease symptoms:

hepatosplenomegaly
spider naevi
jaundice
palmar erythema
ascites

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8
Q

Investigations for PSC and what do you see on imaging?

A

Raised ALP and GGT
Decreased albumin and raised bilirubin
pANCA
Raised IgM in adults, IgG in children
ERCP beading due to strictures
MCRP
Liver biopsy for staging of the disease

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9
Q

PSC management - acute, chronic

A

Acute management - fluids, Abx
Medical - Symptom control - Colestyramine for pruritis, calcium, fat soluble vitamins, ECRP
Liver transplant

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10
Q

Primary sclerosing cholangitis - complications

A

Recurrent cholangitis, biliary cirrhosis, cholangiocarcinoma, portal HTN

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