Small Bowel Disorders Flashcards

1
Q

What are differentials for Angiodyplasia?

A
  • GI malignancies
  • Diverticular Disease
  • Oesophageal Varices
  • Coagulopathies
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2
Q

What is Angiodysplasia?

A

Most common vascular abnormality of GI tract.

Responsible for GI bleeds.

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3
Q

What is the pathophysiology of Angiodysplasia?

A
  • Caused by formation of arteriovenous malformation between previously healthy blood vessels, most commonly caecum and ascending colon.
  • Can be divided into acquired and congenital
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4
Q

What is Acquired Angiodysplasia?

A
  • Begins as reduced submucosal venous drainage in colon due to chronic and intermittent contraction of the colon, giving rise to dilated and tortuous veins.
  • Results in loss of pre-capillary sphincter competency and in turn causes the formation of small arterio-venous communication characterized by small tuft of dilated vessels.
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5
Q

What is Congenital Angiodysplasia?

A

-Hereditary haemorrhagic telangectasia (Rendu-Osler-Weber syndrome) or Herde’s syndrome

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6
Q

What are clinical features of Angiodysplasia?

A
  • Rectal bleeding which can be haemorrhagic or painless occult bleeding
  • Anaemia
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7
Q

What are tests for Angiodysplasia?

A
  • FBC’s
  • U&E’s
  • LFTs
  • Clotting
  • Group and Save or Crossmatch
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8
Q

What imaging tests for Angiodysplasia?

A
  • Upper GI endoscopy performed or colonoscopy
  • In small bowel, wireless capsule endoscopy used with any produce bleeding stemmed via administration of therapeutic agents
  • Mesenteric angiography ordered in setting of overt angiodysplastic bleed. Can involve either radionuclide scanning, CT scanning or MRI scanning to image GI tract vascular supply after radio-opaque contract agent injection into vessels
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9
Q

How is angiodysplasia conservatively managed?

A

Bed-rest and IV fluid support, along with potential tranexamic acid will provide sufficient management due to the self-limiting nature of the condition

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10
Q

How is Angiodysplasia medically managed?

A

Endoscopy – usually first line management. Involves subjecting the bleeding vessel to electrical current and argon acting as a safe, cost-effective, successful treatment option. Other endoscopic techniques include monopolar electrocautery, laser photoablation, sclerotomy, and band ligation

Mesenteric Angiography – used for small bowel lesions that cannot treated endoscopically. Procedure involves super-selective catherization and embolization of the vessel that has been demonstrated to be bleeding by extravasation of contrast dye into the bowel lumen form identified angiodysplastic lesion

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11
Q

What is the surgical management of angiodysplasia?

A

Resection and anastomosis of affected segment of bowel necessary to limit bleeding. Bowel resection in patients with angiodysplasia associated with relatively high mortality thus should only be considered if necessary. Indications are

  • Continuation of severe bleeding despite angiographic and endoscopic management
  • Severe acute life-threatening GI bleeding
  • Multiple angiodysplastic lesions that cannot be treated medically
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12
Q

What are complications of Angiodysplasia?

A
  • Mainly related to the treatment as re-bleeding post therapy is relatively common.
  • Endoscopic techniques have small risk of bowel perforation
  • Mesenteric angiography carries risk of haematoma formation, arterial dissection, thrombosis and bowel ischaemia
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13
Q

What are neuroendocrine tumours?

A

-Gastroenterpancreatic neuroendocrine tumours (GEP-NETs) are neuroendocrine tumours arising from neuroendocrine cells in the tubular GI tract and the pancreas all of which have malignant potential.

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14
Q

What are the grades of Neuroendocrine tumours?

A

Grade 1 – Well differentiated, mitotic count <2 per 10HPF, ki index <3%\

Grade 2 – Well differentiated, mitotic count 2-20 per 10HPF, ki index 3-20%

Grade 3 – Poorly differentiated, mitotic count >20 per 10HPF, ki index >20%

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15
Q

What are risk factors for Neuroendocrine tumours?

A

Genetics.

Inherited disorders such as Multiple Endocrine neoplasia type 1 (MEN1, von Hippel-Lindau disease, neurofibromatosis and tuberous sclerosis complex

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16
Q

What are clinical features of Neuroendocrine Tumours?

A
  • Vague Abdominal Pain
  • Nausea
  • Vomiting
  • Abdominal Distension
  • Ujtietional weight loss
  • Palpable abdominal mass
17
Q

What can well differentiated GEP-NETs develop into?

A

Carcinoid Syndrome which is as a result of over secretion of bioactive mediators such as serotonin, prostaglandins and gastrin into circulation. Present with:

  • Flushing
  • Abdominal Pain
  • Diarrhoea
  • Wheezing
  • Palpatation
18
Q

What are investigations for neuroendocrine tumours?

A

Bloods

  • Chromogranin A and 5-HIAA levels checked
  • Routine blood including FBC and LFTs.
  • Chromogranin B and pancreatic peptide can also be useful.
  • Genetic testing should be considered if clinical history suggestive

Imaging

  • Endoscopy
  • CT enterocolysis
19
Q

How are Gastroenteropancreatic Neuroendocrine tumours managed?

A

-Surgery via Resection of tumours

20
Q

What is Zollinger-Ellison syndrome?

A

Zollinger-Ellison syndrome is condition characterised by excessive levels of gastrin, usually from a gastrin secreting tumour usually of the duodenum or pancreas.
Around 30% occur as part of MEN type I syndrome

21
Q

What are features of Zollinger-Ellison syndrome?

A
  • multiple gastroduodenal ulcers
  • diarrhoea
  • malabsorption
22
Q

How is diagnosis of Zollinger-Ellison syndrome made?

A
  • fasting gastrin levels: the single best screen test

* secretin stimulation test