Reye syndrome and liver transplantation.

Abstract

Reye syndrome is a rare, but severe and often fatal disease. The etiology of the classical Reye syndrome is unknown, but it is typically preceded by a viral infection with a free interval of three to five days. The main physiopathological hypothesis is a mitochondrial metabolism insult causing acute liver failure and encephalopathy. Survivors present serious neurological sequelae. The treatment of Reye syndrome is usually medical with intensive care management. Herein, we present the clinical case of a six-month-old baby diagnosed with Reye syndrome with a fulminant hepatitis, who was successfully liver transplanted with an auxiliary partial orthotopic liver transplantation.

• Authors: Murat Cağ, Anne-Catherine Saouli, Maxime Audet, Philippe Wolf, Jacques Cinqualbre
• Journal: The Turkish journal of pediatrics (Turk J Pediatr) 2010 Nov-Dec Vol. 52 Issue 6 Pg. 662-4 ISSN: 0041-4301 [Print] Turkey
• PMID: 21428204 (Publication Type: Case Reports, Journal Article)

Chemical References

• Anti-Inflammatory Agents, Non-Steroidal
• Aspirin

Topics

• Anti-Inflammatory Agents, Non-Steroidal (adverse effects)
• Aspirin (adverse effects)
• Humans
• Infant
• Liver Failure, Acute (chemically induced, surgery)
• Liver Transplantation
• Male
• Reye Syndrome (chemically induced, pathology, physiopathology, surgery)