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Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS): a case report in Thailand.
Article in English | IMSEAR | ID: sea-45158
ABSTRACT
Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital disease with high mortality rate. The authors report a case of a female term infant with massive abdominal distension at birth. Abdominal ultrasonography revealed a huge cystic mass resolved after urinary catheterization. Exploratory laparotomy was performed and intraoperative findings were an enlarged urinary bladder, microcolon, short bowel and malrotation of the small intestine. Ladd's procedure, ileostomy and vesicostomy were performed. Pathological findings of rectal biopsy revealed normal ganglion cells. Although prokinetic drugs were given for promoting bowel motility, enteral feedings were not tolerated. She died from septicemia at the age of 50 days.
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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Peristalsis / Syndrome / Thailand / Abnormalities, Multiple / Urinary Bladder / Female / Humans / Infant, Newborn / Colon Country/Region as subject: Asia Language: English Year: 2004 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Peristalsis / Syndrome / Thailand / Abnormalities, Multiple / Urinary Bladder / Female / Humans / Infant, Newborn / Colon Country/Region as subject: Asia Language: English Year: 2004 Type: Article