Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: Liver transplantation in a patient with S beta degrees-thalassemia
Author: Gilli, SCO
Boin, IFS
Leonardi, LS
Luzo, ACM
Costa, FF
Saad, STO
Abstract: Background. Patients presenting sickle cell disease may develop different types of hepatic complications. Intrahepatic cholestasis is a potentially fatal complication of the disease, and sometimes the only possible solution is transplantation. Postoperative transfusion management has not yet been well established. In this report, we describe the transfusional program of a patient presenting sickle cell disease and intrahepatic cholestasis who underwent liver transplantation 2 years ago. Methods. Data were obtained from the chart. and the blood bank records. Results. The liver transplantation was performed successfully. Despite mild allograft dysfunction 3 months after surgery, secondary to intrahepatic sickling, the patient has been doing well with the transfusional management adopted (sickle-cell hemoglobin <20%). Conclusion. Sickle cell disease should not be a criterion for exclusion from liver transplantation. Regular transfusion with monitoring of sickle-cell hemoglobin is a very important measure to minimize the risk of intrahepatic sickling and possible rejection.
Country: EUA
Editor: Lippincott Williams & Wilkins
Citation: Transplantation. Lippincott Williams & Wilkins, v. 74, n. 6, n. 896, n. 898, 2002.
Rights: fechado
Identifier DOI: 10.1097/01.TP.0000028445.23375.FA
Date Issue: 2002
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.