THE BIANCHI PROCEDURE IN A PATIENT WITH JEJUNAL ATRESIA

Citation
H. Flageole et al., THE BIANCHI PROCEDURE IN A PATIENT WITH JEJUNAL ATRESIA, European journal of pediatric surgery, 7(6), 1997, pp. 361-363
Citations number
18
ISSN journal
09397248
Volume
7
Issue
6
Year of publication
1997
Pages
361 - 363
Database
ISI
SICI code
0939-7248(1997)7:6<361:TBPIAP>2.0.ZU;2-P
Abstract
While small-bowel transplantation remains an option for the management of short-bowel syndrome (SBS), every effort must be made to optimize the function of the native bowel. This report describes a patient with SBS who dramatically improved after a Bianchi procedure. The patient was born with type IIIb jejunal atresia, complicated by volvulus of th e terminal ileum. He was left with 40 cm of small bowel and his ileoce cal valve. During the first 20 months of his life, he was always hospi talized except for 3 months. He was on parenteral nutrition (TPN) and suffered multiple episodes of central line sepsis. Massive small-bowel dilatation caused a functional bowel obstruction with bacterial overg rowth, and villous atrophy of the jejunal mucosa was discovered on bio psies done by colonoscopy. In March 1994, we elected to proceed with a Bianchi procedure. Thirty cm of jejunum were divided longitudinally. During the following year, his enteral tolerance steadily improved to the point where TPN could be discontinued.