[Liver transplantation in an adolescent with cystic fibrosis]

Arch Pediatr. 1996 Dec;3(12):1248-52. doi: 10.1016/s0929-693x(97)85936-2.
[Article in French]

Abstract

Background: Orthotopic liver transplantation (OLT) is an effective treatment for patients with cystic fibrosis end stage liver disease, especially those with only mild pulmonary involvement. Long-term follow-up in such transplanted patients is still lacking.

Case report: A 15-year-old girl with cystic fibrosis received an OLT because of severe decompensated cirrhosis. She had been colonized by Pseudomonas aeruginosa for 3 years and had pancreatic insufficiency; she also had mild glucose intolerance. Postoperatively she developed diabetes mellitus requiring insulin therapy for 9 months. Oral cyclosporin was poorly absorbed so that she was given a new emulsion of cyclosporin (Neoral) that was better absorbed. A rapid pubertal catch-up was obtained but the patient remained colonized by Pseudomonas aeruginosa.

Conclusion: This 3-year postoperative follow-up confirms that OLT can represent a good alternative in those patients with severe liver disease and mild pulmonary involvement.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Adolescent
  • Body Constitution
  • Cystic Fibrosis / complications
  • Cystic Fibrosis / therapy*
  • Female
  • Humans
  • Liver Cirrhosis / complications
  • Liver Cirrhosis / surgery
  • Liver Transplantation*
  • Postoperative Period