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.
Original language | English |
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Pages (from-to) | 35-39 |
Number of pages | 5 |
Journal | Intractable and Rare Diseases Research |
Volume | 1 |
Issue number | 1 |
DOIs | |
Publication status | Published - 03-2012 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- General Medicine