Treatment of congenital microgastria and dumping syndrome.

Abstract:

:Two children with congenital microgastria and associated anomalies requiring surgery as infants, developed severe dumping syndrome which necessitated a remedial operation. A Roux-en-Y jejunal pouch (Hunt-Lawrence) was formed at 22 months and 10 months respectively. Weight gain was immediate in both patients and has been sustained for 6 months and 8 years respectively. Symptoms of the dumping syndrome were relieved and the pouch delays filling of the jejunum.

journal_name

J Pediatr Surg

authors

Anderson KD,Guzzetta PC

doi

10.1016/s0022-3468(83)80017-7

subject

Has Abstract

pub_date

1983-12-01 00:00:00

pages

747-50

issue

6

eissn

0022-3468

issn

1531-5037

pii

S0022346883001438

journal_volume

18

pub_type

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