Gastro Flashcards
What’s the rule for PBC?
The M rule:
IgM
anti-Mitochondrial ab M2
Middle aged females
Early signs - asymptomatic eg raised ALP on routine LFTs, fatigue pruritis
Suggestive of?
PBC
What other conditions is PBC associated with?
Sjogren’s syndrome (seen in up to 80% of patients)
rheumatoid arthritis
systemic sclerosis
thyroid disease
When for liver transplant in PBC?
Bilirubin >100
Histology showing:
inflammation in all layers from mucosa to serosa
goblet cells
granulomas
Suggestive of?
Crohns
Diarrhoea, weight loss, arthralgia, lymphadenopathy, ophthalmoplegia - what condition? cause? more common in who?
Whipples disease - Infection by tropheryma whipplei
More common in HLA B27 +ve and middle aged MEN
jejunal biopsy shows deposition of macrophages containing Periodic acid-Schiff (PAS) granules - which disease?
Whipples disease
Severity of UC flare ups?
mild: < 4 stools/day, only a small amount of blood
moderate: 4-6 stools/day, varying amounts of blood, no systemic upset
severe: >6 bloody stools per day + features of systemic upset (pyrexia, tachycardia, anaemia, raised inflammatory markers)
Mx of severe UC colitis?
Admission + IV steroids
(IV ciclosporin if CI)
If no improvement in 72h consider adding IV ciclosporin / surgery
Flushing, diarrhoea, bronchospasm, tricuspid stenosis, pellagra
Diagnosis? ix? mx?
Carcinoid syndrome
Ix - Urinary 5-HIAA + plasma chromogranin A y
Mx - Somatostatin analogue (octretride)
- Cyproheptadine may help with diarrhoea
biospy shows pigment laden macrophages in someone having diarrhoea is suggestive of? Colonscopy findings?
Laxative abuse (esp Senna)
Colonoscopy - dark-brown discolouration in the proximal colon (Melanosis coli)
What needs to be offered to everyone with Coeliac, how often and why?
Pneumococcal vaccination 5 yearly due to functional hyposplenism
Grading of hepatic encephalpathy?
Grade I: Irritability
Grade II: Confusion, inappropriate behaviour
Grade III: Incoherent, restless
Grade IV: Coma
Prophylaxis of hepatic encephalopathy?
Lactulose (increased excretion and metabolism of ammonia)
Can also add Rifaximin (Modulates gut flora -> decreased ammonia production)
Suspected pathophysiology of hepatorenal syndrome?
Sphlanchnic vasodilation -> underfilling of kidneys
Noticed by juxtaglomerular apparatus -> RAAS activation -> Renal vasoconstriction (doesn’t counterbalance enough)
Difference between Type 1 and 2 Hepatorenal syndrome?
Type 1 - rapidly progressive - v. poor prognosis
Type 2 - slowly progressive - poor prognosis but better than type 1
Electrolyte abnormalities in refeeding syndrome?
Hypophosphataemia (HALLMARK)
-> muscle weakness inc cardiac (-> cardiac failure) and diaphragm (-> resp failure)
Hypokalaemia
Hypomagnesaemia (can lead to trosades de pointes)
Abnormal fluid balance
Mode of transmission - C Diff
Faecoral via ingestion of spores
Markers of pancreatitis severity?
age > 55 years
hypocalcaemia
hyperglycaemia
hypoxia
neutrophilia
elevated LDH and AST
mx of eosinophilic oesophagitis?
Dietary modification + topical steroids
Oesophageal dilatation - reduces sx associated with strictures
Signs of life threatening C Diff? Mx?
Hypotension
Partial or complete ileus
Toxic megacolon, or CT evidence of severe disease
Mx: Oral Vanc + IV Metro