Gastro 9.5 Flashcards
(120 cards)
Hydatid cysts - tapeworm parasite Echinococcus granulosis - outer fibrous capsule formed containing multiple small daughter cysts
- what type of reaction?
- clinical features?
- Ix?
- Rx?
- cysts are allergens -> type 1 hypersensitivity reaction
- 90% in liver & lungs, Sx if >5cm
- morbidity: cyst bursting, infection, organ dysfunction & anaphylaxis
- if rupture: biliary colic, jaundice, urticaria
- CT to differentiate hydatid vs amoebic vs pyogenic
- Surgery ( do not rupture cyst wall, sterilise contents first)
Causes of acute pancreatitis
Gallstones
ETOH
Trauma
Steroids
Mumps, coxsackie B
Autoimmune (IgG4) eg PAN, Ascaris infection
Scorpion venom
Hypertriglyceridaemia, hyperchlyomicronaemia, hypercalcaemia, hypothermia
ERCP
Drugs: azathioprine, mesalazine, furosemide, bendroflumethiazide, valproate, pentamidine
Achalasia = failure of LOS to relax & oesophageal peristalsis due to degenerative loss of ganglia from Auerbach’s plexus -> LOS contracts, oesophagus above dilates. Middle-age
Features?
Ix?
Rx?
- dysphagia solids & liquids, variation in severity, heartburn, regurgitation, malignant change in small number
- Dx = manometry: XS LOS tone doesn’t relax on swallow
- also barium swallow: fluid level, birds beak, corkscrew; CXR: wide mediastinum, fluid level
- Rx = intra-sphincteric injection of botulinum, Heller cardiomyotomy, balloon dilation
- Drugs to help lower oesophageal pressure = calcium channel blockers, nitrates
Max dose of 1% lidocaine for a 66kg person?
Lidocaine = rapid onset of action, anaesthesia lasts 1h
- what is the max safe dose?
- and if mixed with adrenaline?
20ml of 1% or 10ml 2% lidocaine solution
- 3mg/kg
- adrenaline increases duration of action and reduces blood loss 2ry to vasoconstriction - NEVER use near extremities (ischaemia)
What are the absorbable sutures? When do they disappear?
PDS
Dexon
Vicryl
- usually disappear after 7-10days
What are the non-absorbable sutures? when are the usually removed?
Silk Novafil Prolene Ethilon - usually 7-14days face 3-5 scalp, limbs, chest 7-10 hand, foot, back 10-14
3 types of colon cancer?
sporadic 95%
- series of genetic mutations; >50% show allelic loss of APC gene
- others inc activation of K-ras oncogene, p52 deletion & DCC tumour suppressor genes -> invasive car
HNPCC 5%
FAP <1%
HNPCC 5% of bowel ca
= auto Dom, poorly diff, highly aggressive
- 7 mutations - genetics?
- amsterdam criteria?
- affect genes involved in DNA mismatch repair -> micro satellite instability
- MSH2 60%; MLH1 30%
- higher risk of other cancers e.g. endometrial
- at least 3 family members with colon ca
- cases span 2+ generations
- at least 1 case Dx before age 50
FAP = A. dom bowel ca <1%
- hundreds of polyps by age 30-40 -> carcinoma
- genetics?
- Gardners syndrome?
- APC tumour supp gene mutation on chr 5
- analyse DNA from WBCs
- total colectomy with ileo-anal pitch in their 20s
- at risk of duodenal tumours
Gardners = FAP + osteomas of skull & mandible, retinal pigmentation, thyroid ca, epidermoid cysts of skin
PBC = autoimmune damage to interlobular bile ducts due to chronic inflamm -> progressive cholestasis with may progress to cirrhosis - itching in middle aged F Ass? Dx? Rx? Complications?
- Sjogrens 80%, RA, systemic sclerosis, thyroid disease
- AMA M2 subtype 98%, smooth m Ab 30%, raised serum IgM
- cholestyramine for itch, fat-soluble vitamins, ursodeoxycholic acid, liver Tx if Bili >100 (graft recurrence can occur but not usually a problem)
- cirrhosis
- osteomalacia & osteoporosis
- significantly inc risk of HCC
Budd-Chiari = hepatic vein thrombosis
Features?
Causes?
Ix?
- sudden onset severe abdo pain
- ascites
- tender hepatomegaly
- procoagulant: PRV, OCP, pregnancy, thrombophilia: activated protein C resistance, antithrombin III deficiency, protein C&S deficiencies
Ix = Doppler flow studies
Carcinoid syndrome usually occurs when mets in the liver release serotonin into systemic circulation
- may also occur with lung carcinomas as mediators aren’t ‘cleared’ by the liver
Features?
Ix?
Rx?
- flushing earliest, diarrhoea, bronchospasm, hypotension, right heart valvular stenosis (left can be affected in bronchial carcinoid)
- ACTH & GHRH eg Cushings
- pellagra rarely (dietary tryptophan -> serotonin)
Ix: urinary 5-HIAA, plasma chromogranin A y
Rx = somatostatin analogues eg octreotide, cyproheptadine may help diarrhoea
Flushing earliest, diarrhoea, bronchospasm, hypotension, right heart valvular stenosis
Dx?
carcinoid syndrome
Long Hx of diarrhoea with signs consistent of tricuspid regurgitation
- Dx?
- path findings of heart disease?
Carcinoid syndrome = paraneoplastic syndrome caused by endogenous secretion of serotonin
- endocardial plaques of fibrous tissue that may involve: tricuspid, pulmonary, cardiac chambers, venue cave, PA & coronary sinus
Resuscitation in upper GI bleed?
ABCDE
- platelets if <50
- FFP if fibrinogen <1 or PT/APTT >1.5
- PCC if bleeding on warfarin
- OGD immediately if severe, otherwise within 24h
- PPIs AFTER OGD if non-variceal with bleed on ogd
- repeat OGD, IR/surgery if further bleed
- Pre-OGD consider terlipressin & proph Abx
- band ligation for oesophageal varices
- N-butyl-2-cyanoacrylate injections if gastric varices
- TIPS if varical bleeding not controlled
Chronic pancreatitis affects exocrine & endocrine function
- causes?
- features?
- Ix?
- Rx?
- 80% ETOH, 20% unexplained
- genetic = CF, haemochromatosis
- ductal obstruction: tumours, stones, structural abnormalities inc pancreas divisum & annular pancreas
- pain worse after meal, steatorrhoea, diabetes
- AXR: pan calcification
- CT 85% spec 80% sens
- faecal elastase can assess exocrine function
Rx = enzymes, analgesia, antioxidants
Aspirin in pts following upper GI bleed in whom haemostasis has been achieved?
Continue aspirin when it is being used for 2ry prevention of vascular events
Coeliac disease: gluten enteropathy leading to villous atrophy -> malabsorption
- dermatitis herpetiformis, T1DM, AIhepatitis
Dx?
Ix?
Dx = immunology & jejunal Bx
- villous atrophy & immunology normally reverses on a gluten-free diet
- anti-TTG 1st choice most specific
- anti-endomyseal (but it is IgA)
- anti-gliadin (IgA/IgG) NOT recommended by NICE
- anti-casein found in some
Duodenal Bx: subtotal villous atrophy, crypt hyperplasia, increase in intraepithelial lymphocytes, lamina propria infiltration with lymphocytes
Gilbert’s syndrome: autosomal rec of defective bilirubin conjugation due to deficiency of UDP glucuronosyltransferase in 1-2%
features?
Ix?
- unconjugated hyperbilirubinaemia (not in urine)
- jaundice in response to phys stress eg exercise, illness, fasting
- Rise in bilirubin following prolonged fasting or IV nicotinic acid
33F 4 days increasing lethargy, reduced exercise tolerance, dark urine.
PMH: UC, started sulfasalazine recently for a flare, had been well controlled with no immunosuppressants
O/e conjunctival pallor, abdo DNT, resp/cardio/neuro normal except for a mild systolic murmur & sinus tachycardia. Rectal exam empty, no oral ulcers
Hb 89
MCV 85
Plts 356
WCC 12.1
CRP 30
LDH 2400
Blood film: Heinz bodies, reticulocytsosis
Most appropriate immediate Rx?
Stop Sulfasalazine
- Heinz bodies = small inclusion bodies in RBCs due to oxidative damage to Hb
- sulfasalazine, dapsone, ribavirin & paraquat ingestion poisoning leads to oxidation of Fe2+ to Fe3+, forming metHb
- when overwhelmed, RBCs undergo oxidative damage & cell death -> haemolysis -> raised LDH++
- metHb is converted to hemichromes & eventually precipitated to Heinz bodies
Rx of oxidative haemolytic anaemia = stop offending drug, bloods should normalise within weeks
(transfusion prior to stopping drug would result in further haemolysis)
Wilsons disease = A recessive XS copper deposition in tissues -> increased copper absorption from small bowel & decreased hepatic copper excretion into bile
- defect in ATP7B gene on chr 13
- onset of Sx between 10-25yrs
- children: liver disease; young adults: neuro disease
Features?
Dx?
Rx?
- hepatitis, cirrhosis
- basal ganglia degeneration, speech, behavioural & psych problems, anxiety, chorea, dementia
- cornea: Kayser-Fleischer rings
- blue nails, haemolysis
- kidneys: RTA type 2
, Fanconi: aminoaciduria, glycosuria, phosphaturia - reduced serum caeruloplasmin, reduced serum copper, increased 24h urinary copper excretion
- Rx = Penicillamine (chelates copper) or TRIENTINE hydrochloride eg if penicillin allergy
- tetrathiomolybdate under Ix
Extra-intestinal manifestations of IBD related to disease activity?
arthritis: pauciarticular
erythema nodosum
episcleritis (CD)
osteoporosis
Extra-intestinal manifestations of IBD unrelated to disease activity?
arthritis: symmetric, polyarticular uveitis (UC) pyoderma gangrenosum clubbing PSC (UC)
Pathology in UC?
Barium enema in UC?
- raw red mucosa that bleeds easily, no inflammation beyond submucosa unless fulminant
- widespread ulceration with preservation of adjacent mucosa (pseudo polyps)
- inflammatory cell infiltrate in lamina propria
- neutrophils migrate through walls of glands to form crypt abscesses
- goblet cell depletion & mucin from gland epithelium
Barium enema: loss of haustra, superficial ulcers/pseudopolyps, long standing disease: drainpipe short & narrow colon
Nb pts more likely to be pANCA +ve