| Literature DB >> 25343071 |
Keiichi Uchida1, Kohei Otake1, Mikihiro Inoue1, Yuhki Koike1, Kohei Matsushita1, Toshimitsu Araki1, Yoshiki Okita1, Koji Tanaka1, Katsunori Uchida2, Noriko Yodoya3, Shotaro Iwamoto3, Katsuhiro Arai4, Masato Kusunoki1.
Abstract
Lymphocytic intestinal leiomyositis is a rare entity, which causes chronic intestinal pseudo-obstruction (CIPO) in children. We present the first case of a boy who had pure red cell anemia 1 year before onset. Prolonged ileus developed after gastroenteritis and the patient was diagnosed using a biopsy of the intestinal wall. Findings from the present case indicate that there are three important factors for accurate diagnosis: history of enteritis, positive serum smooth muscle antibody, and lymphocyte infiltration with muscle destruction in the muscularis propria in the intestinal wall. Earlier diagnosis and induction of immunosuppressive therapy may be essential for a better outcome.Entities:
Keywords: Chronic intestinal pseudo-obstruction (CIPO); intestine; leiomyositis; pseudo-obstruction
Year: 2012 PMID: 25343071 PMCID: PMC4204587 DOI: 10.5582/irdr.2012.v1.1.35
Source DB: PubMed Journal: Intractable Rare Dis Res ISSN: 2186-3644