Small Bowel 2 Flashcards

1
Q

what is angiodysplasia

A

vascular abnormality of the GI tract

caused by the formation of arteriovenous malformations between previously healthy blood vessels

presents with rectal bleeding

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2
Q

where is angiodysplasia most commonly found

A

caecum and ascending colon

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3
Q

pathophysiology of acquired angiodysplasia

A

reduced submucosal venous drainage in the colon due to chronic intermittent contraction of the colon, giving rise to dilated and tortuous veins

this results in loss of pre-capillary sphincter competency and in turn causes the formation of small arteriovenous communications characterised by a small tuft of dilated vessels

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4
Q

clinical features of angiodysplasia

A

rectal bleeding and anaemia - typically presents as painless PR bleeding

chronic angiodysplasia can present with symptoms of anemia such as fatigue, weakness or dyspnoea

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5
Q

difference in symptoms between upper GI bleed vs lower GI bleed

A

upper GI = haematemesis and malaena

lower GI = haematochezia (fresh PR bleeding)

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6
Q

investigations into angiodysplasia

A

routine bloods + clotting screen

exclude malignancy - upper GI endoscopy or colonoscopy

mesenteric angiography can also be used to confirm the location of the lesion

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7
Q

management of angiodysplasia

A

depends on severity - 10% present with major GI bleeds

conservative; IV fluids and bed rest (potentially tranexamic acid), argon plasma coagulation

surgical; bowel resection (last resort in patients with major life-threatening GI bleed)

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8
Q

what is the main artery supplying the jejunum

A

superior mesenteric artery

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9
Q

what are the different sections of small intestine called

A

duodenum, jejunum and ileum

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10
Q

what is the most common initial presentation of a patient with a small bowel tumour

A

abdo pain, vomiting and constipation

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11
Q

from what part of the small intestine do most tumours arise from

A

duodenum

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12
Q

names of benign small bowel tumours vs malignant small bowel tumours

A

benign = adenomas

malignant = adenocarcinomas or neuroendocrine tumours

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13
Q

difference between adenocarcinomas vs neuroendocrine tumours of the small bowel

A

adenocarcinomas commonly affect the duodenum

neuroendocrine tumours most commonly affect the ileum

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14
Q

risk factors for small bowel adenocarcinomas

A

non-modifiable = increasing age, crohn’s, coeliac disease, FAP

modifiable; smoking, obesity, low fibre intake, high red meat intake, alcohol excess

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15
Q

clinical features of small bowel cancer

A

initially asymptomatic - first presents with small bowel obstruction due to luminal narrowing

a palpable mass may be found in 25% of cases

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16
Q

investigations into suspected small bowel cancer

A

CT imaging

if proximal then an upper GI endoscopy can be performed and a histological sample taken via biopsy

17
Q

management of small bowel cancer

A

any symptomatic small bowel tumour requires resection - the type of resection depends on the location

duodenal tumours may require pancreaticduodenectomy (whipple’s procedure)

adjuvant chemo used in metastatic disease

18
Q

when would whipple’s procedure be indicated

A

duodenal tumours

19
Q

when would chemo be used in patients with small bowel disease

A

when it is lymph node positive - i.e. the lymph nodes have become involved

20
Q

what would be the best management option for a previously healthy patient with a lymph node negative small bowel adenocarcinoma

A

wide local small bowel resection

21
Q

what are neuroendocrine cells

A

any cell that receives input from neurotransmitters to release hormones into the bloodstream

22
Q

what are Gastroenteropancreatic neuroendocrine tumours (GEP-NETs)

A

neuroendocrine tumours originating from the neuroendocrine cells within the GI tract or the pancreas

23
Q

how are GEP-NETs further classified

A

into; non-functioning tumours (which have no hormone related clinical features) and functioning tumours (which cause symptoms due to peptide and hormone release)

24
Q

what is Carcinoid syndrome

A

occurs following the metastasis of a carcinoid tumour whereby the metastasised cells begin to oversecrete bioactive mediators, such as serotonin, prostaglandins and gastrin into the circulation

present with symptoms of flushing, palpitations, abdo pain, diarrhoea

25
what specific blood tests need to be done to detect a GEP-NET
chromogranin A and 5-HIAA levels also pancreatic polypeptide (PP) (+ endoscopic and CT imaging)
26
management of GEP-NETs
only curative option is surgery those with metastatic disease - palliative chemo alone is typically advised
27
what medication is used in symptomatic control of carcinoid syndrome to avoid carcinoid crisis
somatostatin analogues
28
what is carcinoid crisis
caused by an overwhelming release of hormones from the NET, resulting in resistant severe hypotension