Megacystis microcolon intestinal hypoperistalsis syndrome.
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1999-11-08
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Abstract
Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a rare cause of intestinal obstruction mainly affecting female neonates. We present a case of a newborn female infant with a history of abdominal distension, bilious vomiting and decreased urine output. Barium enema showed a microcolon. Patient died soon after admission and the autopsy revealed a shortened bowel, a microcolon with abundant ganglion cells in the myenteric plexus, and an enlarged urinary bladder. An interesting finding in this case was the presence of enlarged nerve bundles containing several large ganglion cells on the lateral wall of the cervix. The salient clinical and autopsy findings in this case are presented.
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Makhija PS, Magdalene KF, Babu MK. Megacystis microcolon intestinal hypoperistalsis syndrome. Indian Journal of Pediatrics. 1999 Nov-Dec; 66(6): 945-9