Pyloric atresia: 15-year review from a single institution


ILCE Z., ERDOGAN E., KARA C. , Celayir S. , Sarimurat N., SENYUZ O. F. , et al.

JOURNAL OF PEDIATRIC SURGERY, cilt.38, ss.1581-1584, 2003 (SCI İndekslerine Giren Dergi)

  • Cilt numarası: 38 Konu: 11
  • Basım Tarihi: 2003
  • Doi Numarası: 10.1016/s0022-3468(03)00565-7
  • Dergi Adı: JOURNAL OF PEDIATRIC SURGERY
  • Sayfa Sayısı: ss.1581-1584

Özet

Background: Pyloric atresia (PA) is a rare pathology. Calder presented the first pyloric atresia case in 1749 and Touroff, Sussman, Meltz, and their colleagues presented the first successful operation in 1940. PA has 3 types of anatomic variations: (1) type A, pyloric membrane or web; (2) type B, the pyloric channel is a solid cord; and (3) type C, in which there is a gap between the stomach and duodenum. Associated anomalies also have been described. Epidermolysis bullosa (EB) and intestinal anomalies occur most often with this condition.