| Literature DB >> 23139618 |
Keita Fukuyama1, Yasuhide Ishikawa, Tetsuro Ogino, Hidenobu Inoue, Ryoya Yamaoka, Tetsuro Hirose, Tomohiko Nishihira.
Abstract
This report presents a case of massive mucosal necrosis of the small intestine in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS), which particularly affects the brain, nervous system and muscles. A 45-year-old Japanese female, with an established diagnosis of MELAS, presented with vomiting. Computed tomography showed portomesenteric venous gas and pneumatosis intestinalis. She underwent a resection of the small intestine. A microscopic study showed necrosis of the mucosa and vacuolar degeneration of smooth muscle cells in the arterial wall. Immunohistochemistry showed anti-mitochondrial antibody to be highly expressed in the crypts adjacent the necrotic mucosa. The microscopic and immunohistochemical findings suggested the presence of a large number of abnormal mitochondria in MELAS to be closely linked to mucosal necrosis of the small intestine.Entities:
Keywords: Acute mesenteric ischemia; Anti-mitochondrial antibody; Immunohistochemistry; Myopathy, encephalopathy, lactic acidosis, and stroke-like episodes syndrome; Pathology
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Year: 2012 PMID: 23139618 PMCID: PMC3491609 DOI: 10.3748/wjg.v18.i41.5986
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742