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Living Donor Liver Transplantation for Unresectable Liver Adenomatosis Associated with Congenital Absence of Portal Vein: A Case Report and Literature Review
Patient: Female, 21 Final Diagnosis: Unresectable liver adenomatosis associated with congenital absence of portal vein Symptoms: — Medication: — Clinical Procedure: Living donor liver transplantation Specialty: Transplantology OBJECTIVE: Rare disease BACKGROUND: Abernethy malformation (AM), or conge...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581685/ https://www.ncbi.nlm.nih.gov/pubmed/26386552 http://dx.doi.org/10.12659/AJCR.895235 |
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author | Brasoveanu, Vladislav Ionescu, Mihnea Ioan Grigorie, Razvan Mihaila, Mariana Bacalbasa, Nicolae Dumitru, Radu Herlea, Vlad Iorgescu, Andreea Tomescu, Dana Popescu, Irinel |
author_facet | Brasoveanu, Vladislav Ionescu, Mihnea Ioan Grigorie, Razvan Mihaila, Mariana Bacalbasa, Nicolae Dumitru, Radu Herlea, Vlad Iorgescu, Andreea Tomescu, Dana Popescu, Irinel |
author_sort | Brasoveanu, Vladislav |
collection | PubMed |
description | Patient: Female, 21 Final Diagnosis: Unresectable liver adenomatosis associated with congenital absence of portal vein Symptoms: — Medication: — Clinical Procedure: Living donor liver transplantation Specialty: Transplantology OBJECTIVE: Rare disease BACKGROUND: Abernethy malformation (AM), or congenital absence of portal vein (CAPV), is a very rare disease which tends to be associated with the development of benign or malignant tumors, usually in children or young adults. CASE REPORT: We report the case of a 21-year-old woman diagnosed with type Ib AM (portal vein draining directly into the inferior vena cava) and unresectable liver adenomatosis. The patient presented mild liver dysfunction and was largely asymptomatic. Living donor liver transplantation was performed using a left hemiliver graft from her mother. Postoperatively, the patient attained optimal liver function and at 9-month follow-up has returned to normal life. CONCLUSIONS: We consider that living donor liver transplantation is the best therapeutic solution for AM associated with unresectable liver adenomatosis, especially because compared to receiving a whole liver graft, the waiting time on the liver transplantation list is much shorter. |
format | Online Article Text |
id | pubmed-4581685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45816852015-10-06 Living Donor Liver Transplantation for Unresectable Liver Adenomatosis Associated with Congenital Absence of Portal Vein: A Case Report and Literature Review Brasoveanu, Vladislav Ionescu, Mihnea Ioan Grigorie, Razvan Mihaila, Mariana Bacalbasa, Nicolae Dumitru, Radu Herlea, Vlad Iorgescu, Andreea Tomescu, Dana Popescu, Irinel Am J Case Rep Articles Patient: Female, 21 Final Diagnosis: Unresectable liver adenomatosis associated with congenital absence of portal vein Symptoms: — Medication: — Clinical Procedure: Living donor liver transplantation Specialty: Transplantology OBJECTIVE: Rare disease BACKGROUND: Abernethy malformation (AM), or congenital absence of portal vein (CAPV), is a very rare disease which tends to be associated with the development of benign or malignant tumors, usually in children or young adults. CASE REPORT: We report the case of a 21-year-old woman diagnosed with type Ib AM (portal vein draining directly into the inferior vena cava) and unresectable liver adenomatosis. The patient presented mild liver dysfunction and was largely asymptomatic. Living donor liver transplantation was performed using a left hemiliver graft from her mother. Postoperatively, the patient attained optimal liver function and at 9-month follow-up has returned to normal life. CONCLUSIONS: We consider that living donor liver transplantation is the best therapeutic solution for AM associated with unresectable liver adenomatosis, especially because compared to receiving a whole liver graft, the waiting time on the liver transplantation list is much shorter. International Scientific Literature, Inc. 2015-09-19 /pmc/articles/PMC4581685/ /pubmed/26386552 http://dx.doi.org/10.12659/AJCR.895235 Text en © Am J Case Rep, 2015 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License |
spellingShingle | Articles Brasoveanu, Vladislav Ionescu, Mihnea Ioan Grigorie, Razvan Mihaila, Mariana Bacalbasa, Nicolae Dumitru, Radu Herlea, Vlad Iorgescu, Andreea Tomescu, Dana Popescu, Irinel Living Donor Liver Transplantation for Unresectable Liver Adenomatosis Associated with Congenital Absence of Portal Vein: A Case Report and Literature Review |
title | Living Donor Liver Transplantation for Unresectable Liver Adenomatosis Associated with Congenital Absence of Portal Vein: A Case Report and Literature Review |
title_full | Living Donor Liver Transplantation for Unresectable Liver Adenomatosis Associated with Congenital Absence of Portal Vein: A Case Report and Literature Review |
title_fullStr | Living Donor Liver Transplantation for Unresectable Liver Adenomatosis Associated with Congenital Absence of Portal Vein: A Case Report and Literature Review |
title_full_unstemmed | Living Donor Liver Transplantation for Unresectable Liver Adenomatosis Associated with Congenital Absence of Portal Vein: A Case Report and Literature Review |
title_short | Living Donor Liver Transplantation for Unresectable Liver Adenomatosis Associated with Congenital Absence of Portal Vein: A Case Report and Literature Review |
title_sort | living donor liver transplantation for unresectable liver adenomatosis associated with congenital absence of portal vein: a case report and literature review |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581685/ https://www.ncbi.nlm.nih.gov/pubmed/26386552 http://dx.doi.org/10.12659/AJCR.895235 |
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