A valid treatment option for isolated congenital microgastria.

Autor: Zamakhshary, Mohammad, Oda, Omar, Alrabeeah, Abdullah, Al Jadaan, Saud, Al-Namshan, Mohammad, Crankson, Stanley, Hasosah, Mohammed, Aljohani, Othman, Abdulwahab, Ahmed
Zdroj: Annals of Pediatric Surgery; Jul2011, Vol. 7 Issue 3, p114-116, 3p
Abstrakt: Congenital microgastria (CM) is an extremely rare anomaly of the caudal part of the foregut. Treatment of CM has not yet been standardized. We present the case of a 34-month-old girl with an isolated CM complicated by nasogastric tube-related gastric perforation. During the definitive reconstructive surgery, a scarred structure (1.5×1.5 cm) was found to follow a dilated esophagus. The scarred microstomach was resected, and a Roux-en-Y esophagojejunostomy was performed. The patient has been followed for 6 months. She tolerates a regular oral diet and has reached acceptable growth parameters. We describe the first case of CM to be treated with resection of the microstomach and with a Roux-en-Y esophagojejunostomy. [ABSTRACT FROM AUTHOR]
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