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Systemic Amyloidosis: A Rare Presentation of Mesenteric Angina
Author(s) -
Christopher N. Andrews,
Jack Amar,
Malcolm Hayes,
Robert Enns
Publication year - 2002
Publication title -
canadian journal of gastroenterology
Language(s) - English
Resource type - Journals
eISSN - 1916-7237
pISSN - 0835-7900
DOI - 10.1155/2002/125806
Subject(s) - medicine , epigastric pain , angina , abdomen , amyloidosis , superior mesenteric artery , abdominal pain , mesentery , autopsy , mesenteric ischemia , radiology , presentation (obstetrics) , angiography , cardiology , surgery , ischemia , myocardial infarction , vomiting
A 64-year-old man presented with an eight-month history of increasing postprandial epigastric pain and a 15 kg weight loss. Computed tomography of the abdomen, panendoscopy and mesenteric angiography failed to explain the cause of the patient's mesenteric angina. Systemic amyloidosis involving intestinal small vasculature without larger arterial involvement was diagnosed at autopsy after the patient died of an asystolic cardiac arrest. Mesenteric angina without evidence of ischemic enteritis or pseudo-obstruction is a rare manifestation of amyloidosis.

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