Intractable Rare Dis Res. 2012;1(1):35-39. (DOI: 10.5582/irdr.2012.v1.1.35)

Chronic intestinal pseudo-obstruction due to lymphocytic intestinal leiomyositis: Case report and literature review.

Uchida K, Otake K, Inoue M, Koike Y, Matsushita K, Araki T, Okita Y, Tanaka K, Uchida K, Yodoya N, Iwamoto S, Arai K, Kusunoki M


SUMMARY

Lymphocytic intestinal leiomyositis is a rare entity, which causes chronic intestinal pseudoobstruction (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.


KEYWORDS: Chronic intestinal pseudo-obstruction (CIPO), pseudo-obstruction, leiomyositis, intestine

Full Text: