Gastro 9.5 Flashcards
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
Hepatic encephalopathy: XS ammonia & glutamine absorption from bacterial breakdown of proteins in gut features? grading? precipitating factors? Rx?
- confusion, asterix (arrhythmic negative myoclonus 3-5Hz), constructional apraxia, triphasic slow waves on EEG, raised ammonia level I irritable II confusion, inappropriate III incoherent, restless IV coma
- infection eg SBP, GI bleed, post-TIPS, constipation, sedatives/diuretics, hypokalaemia, renal failure, increased dietary protein(uncommon)
- Rx the cause
- 1st = regular Lactulose: aim for 3 stools/day and continue for prevention of recurrent episodes
- +/- Rifaximin for 2ry prophylaxis: add-on for prevention of recurrent episodes after the 2nd episode
- lactulose: promotes ammonia excretion & increases metabolism of ammonia by gut bacteria; Rifaximin modulates gut flora -> decreased ammonia production
RUQ pain & malaena & jaundice after liver Bx
Dx?
how?
Haemobilia
- bleeding into biliary tree following connection between splanchnic circulation & intra/extrahepatic biliary system
- eg Bx needle hit splanchnic vein
3rd trimester itching & jaundice?
Rx?
Intrahepatic cholestasis of pregnancy
- ursodeoxycholic acid for Sx relief, weekly LFTs, induction at 37/40
- inc rate of stillbirth
- there can be a prolonged PT & inc tendency to bleed
3rd trimester/immediate post-partum abdo pain, nausea/vomit, headache, jaundice, hypoglycaemia?
Acute fatty liver of pregnancy
- ALT >500
- if severe -> pre-eclampsia
- supportive care, delivery is definitive once stabilised
Causes of ascites with SAAG >11g/L
cirrhosis ETOH hepatitis cardiac mixed massive liver mets fulminant hepatic failure Budd-Chiari portal vein thrombosis vena-occlusive disease myxoedema fatty liver pregnancy
Causes of ascites with SAAG <11g/L
peritoneal carcinomatosis TB peritonitis pancreatic ascites bowel obstruction biliary ascites post-op lymphatic leak serositis in CT diseases
Rx of ascites?
- reduce dietary sodium
- fluid restrict if na <125
- AA eg spironolactone
- drain if tense (therapeutic abdo paracentesis)
- proph Abx to reduce risk of SBP: Ciprofloxacin/norfloxacin if ascitic protein 15 or less, until ascites has resolved
- consider TIPS in some
Nb paracentesis is not C/I in pts with abnormal clotting - most will have prolonged PT & some thrombocytopenia - but e.g. if severe thrombocytopenia, most would give platelets etc
Paracentesis induced circulatory dysfunction (PICD) - 2ry to fluid shifting after large volumes (>5L) paracentesis -> decreased circulating volume & renal dysfunction
Dx?
Prevention?
- increase of >50% of baseline plasma renin activity to >4ng/ml/h on day 5-6 post paracentesis
- limit volume of fluid removed to 5-6L at a time
- give albumin as a plasma expander if >5L ascitic fluid removed
Crohns disease: INDUCING remission:
- 1st line
- 2nd line
- Add on Rx
- if refractory/fistulating
- if isolated peri-anal disease
- 1st glucocorticoids (or budesonide)
- 2nd 5-ASA eg Mesalazine if steroids not effective
- Add-on Rx e.g. Azathioprine/Mercaptopurine/MTX (not monoRx)
- Infliximab if refractory/fistulating (& cont Azathioprine/mesalazine)
- Metronidazole if isolated peri-anal disease
- enteral feed with elemental diet can help
Crohns disease: MAINTAINING remission?
- stop smoking
- 1st Azathioprine/Mercaptopurine
- 2nd MTX
- consider 5-ASA e.g. mesalazine if pt has had previous surgery
- 80% eventually have surgery
Refeeding syndrome: metabolic abnormalities when feeding someone after a period of starvation - when extended period of catabolism ends abruptly with switching to carb metabolism
What are the metabolic consequences?
Who are considered high risk?
- low phosphate
- low K
- low Mg (torsades)
- abnormal fluid balance
- > organ failure
1+ of:
- BMI<16
- unintentional weight loss >15% over 3-6months
- little nutritional intake >10 days
- low K, phosphate, Mg before feeing
2+ of:
- BMI<18.5
- unintentional weight loss >10% over 3-6months
- little nutritional intake >5days
- Hx of ETOH abuse, drug Rx in insulin, chemo, diuretics, antacids
Nb:
if a pt hasn’t eaten for > 5 days, aim to re-feed at no more than 50% of requirements for the first 2 days
Haemochromatosis: auto rec of iron absorption & metabolism -> ion accumulation - caused by inheritance of HFE gene on both copies of chr 6 - genetic testing of family members - transferrin sat to screen general pop Dx tests? typical iron study profile? Rx?
- molecular genetic testing: C282Y & H63D mutations
- liver B: Perl’s stain
- transferrin sat >55% men or >50% women
- raised ferritin >500 & iron
- low TIBC
Venesection is 1st line - transferrin sat should be kept <50% and ferritin <50
- indicated in all with ferritin >1000
- typical initial regime is 400-500mls every 1-2weeks, then every 2-4months when levels fall to 50-100
Microscopic colitis = chronic inflammatory condition of gut - as common as classic IBD but different
Dx middle-age F>M
RFs?
Features?
RFs = smoking & drugs: NSAIDs, PPIs, SSRIs
- watery diarrhoea
- faecal urgency & incontinence
- abdominal pain
- constitutional Sx
- non-specific findings inc mild anaemia, raised inflame markers, autoAb e.g. RF & ANA
Bile acid malabsorption
- 1ry XS production
- 2ry reduced absorption: ill disease e.g. Crohns, cholecystectomy, coeliac disease, small bowel bacterial overgrowth
- steatorrhoea, vit A, D, E, K malabsorption
Ix?
Rx?
SeHCAT = Ix of choice
- nuclear medicine
- scans 7 days apart to assess retention/loss of radio labelled SeHCAT
Rx with bile acid sequestrates e.g. cholestyramine
Target HbA1c in chronic pancreatitis 2ry to resection?
- both alpha & beta cells removed in pancreatectomy
- reducing intensity of any counter regulatory response to hypoglycaemia
- impacts on prospects of recovery & increases severity of individual events
- so more lax HbA1c target instigated
- eg HbA1c 53
What drug enhances the effects and increases the toxicity of azathioprine?
Allopurinol
- reduce dose of Azathioprine to 1/4 but significant & v specialist
Gastric cancer
- histology?
- Ass?
- features?
- Ix?
- intestinal metaplasia -> dysplasia -> cancer
- TNM staging, risk of LN involvement is related to size & depth of invasion; early cancers confined to submucosa have a 20% incidence of LN metastasis
- signet ring cells: large vacuole of mucin which displaces nucleus to one side, higher numbers = worse prognosis
- H. pylori, blood group A, gastric adenomatous polyps, pernicious anaemia, smoking, diet
- dyspepsia, nausea & vomiting, anorexia & weight loss, dysphagia
Dx = endoscopy & Bx staging = CT or endoscopic US (eUS superior to CT)
Gastric ca tumours of GOJ classification?
type 1 - true oesophageal cancers, may be ass with Barretts
type 2 - carcinoma of cardia, arising from cardiac type epithelium or short segments with intestinal metaplasia at the OGJ
type 3 - subcardial cancers that spread across the junction, involve similar nodal stations to gastric ca
Staging & Rx of gastric ca?
- CT CAP routine 1st line
- laparoscopy to identify occult peritoneal disease
- PET CT esp for junctional tumours
- Subtotal gastrectomy for proximally sited disease 5-10cm from OGJ
- Total gastrectomy if tumour <5cm from OGJ
- Oesophagogastrectomy for type 2 junctional tumours extending into oesophagus
- Endoscopic submucosal resection in early gastric cancer confined to mucosa/submucosa
- Lymphadenectomy/D2 nodal dissection
- Most receive chemo pre/post op
Colorectal ca in UC
- lesions can be multifocal
- factors that increase risk?
- colonoscopy surveillance?
- disease duration >10years, pts with punctilios, onset before 15yrs old, unremitting disease, poor compliance to Rx
Low risk = 5yr colonoscopy
- extensive colitis with no active endoscopic/histological inflammation
- or left-sided colitis
- or Crohns colitis <50% of colon
Intermediate = 3yr colonoscopy
- extensive colitis with mild active inflammation
- or post-inflammatory polyps
- or FHx colorectal ca in 1st degree relative aged 50+
Higher risk = annual colonoscopy
- extensive colitis with mod/severe inflame
- or stricture in last 5yrs
- or dysplasia in last 5yrs declining surgery
- or PSC/Tx for PSC
- or FHx colorectal ca in 1st degree relative <50yrs
UC severity?
Mild - <4stools/day small amount blood
Mod 4-6stools/day varying blood, no systemic upset
Severe >6stools/day + features of systemic upset e.g. fever, tachycardia, anaemia, raised inflammatory markers
UC Rx INDUCING remission?
- Distal/Rectal colitis: Topical aminosalicylates or steroids
- Oral aminosalicylates
- Oral prednisolone 2nd line if aminosalicylates fail - wait 4wks before deciding
IV steroids 1st line for severe colitis
- assess response after 3-5days
- rescue therapy = Infliximab or cyclosporin if disease remains severely active
- if inadequate response of infliximab at day 5-7 then consider colectomy
UC Rx MAINTAINING remission?
- oral aminosaicylate eg mesalazine
- azathioprine & mercaptopurine
- some evidence probiotics may prevent relapse
C diff = gram +ve rod - produces exotoxin which causes bowel damage leading to pseudomembranous colitis
RFs = Abx, PPIs
Features = diarrhoea, abdo pain, raised WBC, toxic megacolon if severe
Dx = CD toxin in stool
Rx?
- oral metronidazole
- oral van if not responding or severe
- fidaxomicin if not responding or multiple comorbidities
- oral vanc + IV metronidazole for life-threatening infections
- Bezlotoxumab is a mAb which targets C diff toxin B
colonoscopy: yellow membranes in an inflamed colon suggests pseudomembranous colitis