Liver transplantation in mitochondrial respiratory chain disorders.

Abstract

UNLABELLED:

Mitochondrial respiratory chain disease may lead to neonatal or late onset liver failure, requiring liver transplantation. In rare cases, the disease is restricted to the liver and the patient is cured after surgery. More frequently, other organs are simultaneously involved and neuromuscular or other extra-hepatic symptoms may pre-exist, or appear in the post-transplant follow up. Pre-transplant evaluation should aim to rule out neurological disease, which may be difficult to differentiate from signs accompanying liver insufficiency. Cerebrospinal fluid lactic acid levels, compared to blood lactate, may be suggestive of central nervous system involvement. Of 11 cases with respiratory chain disorders who had liver transplantation in various centres, 4 are alive and well on follow up, and 6 died, three of them having developed neurological disease post orthotopic liver transplantation. All three patients with initial liver and gastro-intestinal disease died early after transplantation, indicating that these may be poor candidates for this procedure.

CONCLUSION:

Liver transplantation is feasible in hepatic respiratory chain disorders, but extra-hepatic disease should be ruled out before transplantation. Extra-hepatic manifestations may, however, appear and cause patient death despite successful transplantation.

• Authors: E M Sokal, R Sokol, V Cormier, F Lacaille, P McKiernan, F J Van Spronsen, O Bernard, J M Saudubray
• Journal: European journal of pediatrics (Eur J Pediatr) Vol. 158 Suppl 2 Pg. S81-4 (Dec 1999) ISSN: 0340-6199 [Print] Germany
• PMID: 10603105 (Publication Type: Journal Article)

Chemical References

• Lactic Acid

Topics

• Electron Transport
• Female
• Humans
• Hypoglycemia (etiology)
• Infant
• Infant, Newborn
• Lactic Acid (cerebrospinal fluid)
• Liver Failure (etiology, mortality, surgery)
• Liver Transplantation
• Male
• Mitochondria (metabolism)