Successful Treatment of Biliary Atresia in Very Small Infants through Living Related Liver Transplantation

Improving outcomes in very small children is a major goal of pediatric liver transplantation. This report describes our experience of living related liver transplantation in an infant weighing 3.98 kg. The recipient, a 80-day-old male infant with congenital biliary atresia, was treated with living d...

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Main Authors: Chunbao Guo, Mingman Zhang
Format: Article
Language:English
Published: Karger Publishers 2010-05-01
Series:Case Reports in Gastroenterology
Subjects:
Online Access:http://www.karger.com/Article/FullText/314195
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author Chunbao Guo
Mingman Zhang
author_facet Chunbao Guo
Mingman Zhang
author_sort Chunbao Guo
collection DOAJ
description Improving outcomes in very small children is a major goal of pediatric liver transplantation. This report describes our experience of living related liver transplantation in an infant weighing 3.98 kg. The recipient, a 80-day-old male infant with congenital biliary atresia, was treated with living donor liver transplantation and then followed up for 6 months. The left lateral segment (segment II, III) with reduced size from the donor, his 26-year-old mother, was used as the graft. The graft weighed 200 g. The graft weight to recipient body weight ratio was 5.025%. The donor regained her liver function within 3 days and was discharged on day 8. The patient showed good results. Liver function returned to normal 9 days after the operation with bilirubin level almost decreased to normal. Cyclosporin, mycophenolate mofetil and prednisone were used for postoperative immunosuppression. No bleeding, thrombosis, infection or bile leakage occurred. The patient had slight fever because of a little collection in the abdomen and recovered after paracentesis and drainage. He was discharged on day 16. The donor and recipient are in satisfactory condition at present. Improvement of technique in hepatic surgery, microsurgical technique in vascular surgery and postoperative intensive care are the keys to ensure the success of the procedure.
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spelling doaj.art-b58218f0ea6a46f0a2ae968018b76d162022-12-21T23:06:54ZengKarger PublishersCase Reports in Gastroenterology1662-06312010-05-014215816710.1159/000314195314195Successful Treatment of Biliary Atresia in Very Small Infants through Living Related Liver TransplantationChunbao GuoMingman ZhangImproving outcomes in very small children is a major goal of pediatric liver transplantation. This report describes our experience of living related liver transplantation in an infant weighing 3.98 kg. The recipient, a 80-day-old male infant with congenital biliary atresia, was treated with living donor liver transplantation and then followed up for 6 months. The left lateral segment (segment II, III) with reduced size from the donor, his 26-year-old mother, was used as the graft. The graft weighed 200 g. The graft weight to recipient body weight ratio was 5.025%. The donor regained her liver function within 3 days and was discharged on day 8. The patient showed good results. Liver function returned to normal 9 days after the operation with bilirubin level almost decreased to normal. Cyclosporin, mycophenolate mofetil and prednisone were used for postoperative immunosuppression. No bleeding, thrombosis, infection or bile leakage occurred. The patient had slight fever because of a little collection in the abdomen and recovered after paracentesis and drainage. He was discharged on day 16. The donor and recipient are in satisfactory condition at present. Improvement of technique in hepatic surgery, microsurgical technique in vascular surgery and postoperative intensive care are the keys to ensure the success of the procedure.http://www.karger.com/Article/FullText/314195InfantBiliary atresiaLiving donorLiver transplantation
spellingShingle Chunbao Guo
Mingman Zhang
Successful Treatment of Biliary Atresia in Very Small Infants through Living Related Liver Transplantation
Case Reports in Gastroenterology
Infant
Biliary atresia
Living donor
Liver transplantation
title Successful Treatment of Biliary Atresia in Very Small Infants through Living Related Liver Transplantation
title_full Successful Treatment of Biliary Atresia in Very Small Infants through Living Related Liver Transplantation
title_fullStr Successful Treatment of Biliary Atresia in Very Small Infants through Living Related Liver Transplantation
title_full_unstemmed Successful Treatment of Biliary Atresia in Very Small Infants through Living Related Liver Transplantation
title_short Successful Treatment of Biliary Atresia in Very Small Infants through Living Related Liver Transplantation
title_sort successful treatment of biliary atresia in very small infants through living related liver transplantation
topic Infant
Biliary atresia
Living donor
Liver transplantation
url http://www.karger.com/Article/FullText/314195
work_keys_str_mv AT chunbaoguo successfultreatmentofbiliaryatresiainverysmallinfantsthroughlivingrelatedlivertransplantation
AT mingmanzhang successfultreatmentofbiliaryatresiainverysmallinfantsthroughlivingrelatedlivertransplantation