Recombinant growth hormone (GH) has been used successfully to promote mucos
al intestinal adaptation in adults with short bowel syndrome, Here the auth
ors report the case of an infant with extreme short bowel syndrome successf
ully treated with intestinal lengthening and GH. The patient was born with
intestinal atresia leaving only 12 cm of jejunum and 2 cm of ileum with ile
ocecal valve. A Bianchi procedure extended the length to 25 cm, but 6 month
s later she still received 50% of her nutritional requirements by parentera
l route. A 4-week course of 0.5 U/kg of GH dramatically changed the situati
on allowing weaning of total parenteral nutrition (TPN) 2 weeks after the e
nd of the treatment with striking nutritional improvement, decrease in the
number of stools from 7 to 2 per day, and no secondary effects. The authors
believe that GH deserves clinical trial in cases of extreme short bowel. J
Pediatr Surg 34:1423-1424. Copyright (C) 1999 by W.B. Saunders Company.