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Publikováno v:
Journal of Pediatric Surgery, Vol. 43, No 10 (2008) pp. 1932-1934
We describe a new procedure of digestive reconstruction after pylorus-preserving pancreaticoduodenectomy in a 13-year-old girl presenting with a large solid and papillary epithelial neoplasm of the pancreatic head. A midgut transposition (like in a c
Publikováno v:
Journal of Pediatric Surgery. 43:e33-e35
Primary repair of very long gap esophageal atresia (EA) with almost complete absence of thoracic esophagus has usually been thought impossible. Thus, esophageal replacement with colon or gastric interposition seemed inevitable. In contrast, J. Foker
Autor:
Sigrid Caron-Bataille, Ernest Goura, Antoine Mboyo, Benedicte Legrand, Jean Ndié, Muriel Repetto-Germaine, Vincent Flurin, Richard Massicot
Publikováno v:
Journal of Pediatric Surgery. 43:e1-e3
The case of a 2-year-old boy suffering from a strangulated ileal herniation through Winslow's foramen into the lesser sac is reported. He presented an abdominal pain of sudden onset 16 hours previously. The clinical examination, abdominal x-ray, and
Publikováno v:
Journal of Pediatric Surgery. 33:1686-1689
A 12-year-old girl who suffered from cholangitis was treated successfully with appropriate antibiotics. She had undergone an operation in mainland China, the exact nature of which was unknown. After an ultrasound study, she underwent a helical comput
Autor:
Peter Beale, Behrouz Banieghbal
Publikováno v:
Journal of Pediatric Surgery. 42:1362-1364
Aim Jejunal atresia (JA) is a common cause of intestinal obstruction in the newborn. It is corrected by small bowel tapering/excision and end-to-end enteroenterostomy, performed through a transverse laparotomy incision. It has excellent result with m
Autor:
João Gilberto Maksoud, Gilda Porta, Maria Claudia Nogueira Zerbini, Irene Miura, Dario O. Fauza, Marcos Marques da Silva
Publikováno v:
Journal of Pediatric Surgery. 33:115-118
Background/Purpose: The aim of this study was to address the perioperative aspects of hepatoportoenterostomy (HPE) for biliary atresia (BA), through the study of a 15-year, single-center experience of the management of this disease. Methods: One hund
Publikováno v:
Journal of Pediatric Surgery. 41:1973-1975
Purpose This retrospective study reviews the long-term outcome of type I biliary atresia (BA). Methods Three hundred twenty-three patients with BA, including 50 with type I, underwent corrective surgery. The surgical results, role of cholangiograms d
Publikováno v:
Journal of Pediatric Surgery. 41:e1-e3
We present a case report of a boy with biliary atresia who, after hepatoportoenterostomy performed on day 21 of life, had immediate resolution of cholestasis and remained anicteric until 3.5 months of age. He then abruptly developed acholic stools. N
Autor:
Henrik Hedlund
Publikováno v:
Journal of Pediatric Surgery. 32:1717-1720
Background: There is no general agreement about how patients who have short-segment Hirschsprung's disease should be treated. Methods: Ten patients with Hirschsprung's disease, seven with rectal and three with rectosigmoidal aganglionosis, were opera
Publikováno v:
Journal of Pediatric Surgery. 32:1630-1633
Background: Fecal incontinence is common in children who have anorectal malformations, Hirschsprung's Disease, and spina bifida and can negatively impact their emotional and social development. Enemas have been used as an artificial way to keep child