2nd International Symposium on Congenital Anomaly (ISCA). Multidisciplinary Management on Gastrointestinal and Hepatobiliary Anomalies

Khaleddemyati's picture
Research Title: 
Neonatal Gastrointestinal Stromal Tumor
Authors: 
Khaled, D
Country: 
Indonesia
Date: 
Sat, 2008-04-26
Research Abstract: 
Neonatal gastrointestinal stromal tumor (GIST) is very rare in infancy. We report a case;day 2 of life full-term baby girl, with history of vomiting and inability to tolerate feeding. Antenatally, her mother had history of polyhydramnios. On examination, she was dehydrated with scaphoid abdomen with no organomegaly. She had no dysmorphic features. Her abdominal radiograph showed double bubble appearance.the provisionl diagnosis was duodenal atresia and she underwent laparatomy. Operativee finding was a well defined mass obstructing the second part of the duodenum. A gastrojejunoplasty bypass was done. Histopathological interpretation was gastrointestinal stromal tumor (GIST). The tumor showed positive smooth muscle actin (SMA) and S100 protien; however it was negative for CD117 and CD 34. post operative, she is well and recent CT scan reveal the mass is not increasing in size.
keywords: neonatal, gastrointestinal stromal tumor, dudenal atresia,
GIST