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De novo malignancies after liver transplantation: a single-center experience

BACKGROUND AND OBJECTIVES: The recipients of liver transplantation (LT) are subjected to lifelong immunosuppression with its many drawbacks. De novo and recurrent malignancy in transplant recipients are attributed to attenuation of immunosurveillance. In the present study, we present our experience...

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Autores principales: Hegab, Bassem, Khalaf, Hatem, Allam, Naglaa, Azzam, Ayman, Al Khail, Faisal Aba, Al-hamoudi, Waleed, Kamel, Yasser, Al Bahili, Hamad, Al Sofayan, Mohammed, Al-Sebayel, Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2012
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081011/
https://www.ncbi.nlm.nih.gov/pubmed/22705604
http://dx.doi.org/10.5144/0256-4947.2012.355
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author Hegab, Bassem
Khalaf, Hatem
Allam, Naglaa
Azzam, Ayman
Al Khail, Faisal Aba
Al-hamoudi, Waleed
Kamel, Yasser
Al Bahili, Hamad
Al Sofayan, Mohammed
Al-Sebayel, Mohammed
author_facet Hegab, Bassem
Khalaf, Hatem
Allam, Naglaa
Azzam, Ayman
Al Khail, Faisal Aba
Al-hamoudi, Waleed
Kamel, Yasser
Al Bahili, Hamad
Al Sofayan, Mohammed
Al-Sebayel, Mohammed
author_sort Hegab, Bassem
collection PubMed
description BACKGROUND AND OBJECTIVES: The recipients of liver transplantation (LT) are subjected to lifelong immunosuppression with its many drawbacks. De novo and recurrent malignancy in transplant recipients are attributed to attenuation of immunosurveillance. In the present study, we present our experience with de novo malignancies encountered after both deceased and living donor liver transplantations. DESIGN AND SETTING: Retrospective study of patients referred to LT center between April 2001 and January 2010 PATIENTS AND METHODS: Various data were collected including type of malignancy and histopathologic features, immunosuppression regimen, and patient survival. RESULTS: Of 248 LT procedures performed in 238 patients (10 retransplants), 8 patients (3.4%) developed de novo post-LT malignancies. De novo malignancies included post-LT lymphoproliferative disorders (PTLD) in 5 patients who were all Epstein-Barr virus (EBV) positive, and who were treated successfully with anti-CD20 monoclonal antibody therapy, reduction of immunosuppression, and control of EBV activity; urinary bladder cancer in 1 patient who was treated with radical surgical resection and chemotherapy but died of bone and lung metastasis within 1 year of diagnosis; endometrial carcinoma in 1 patient who was treated with radical surgical resection; and Kaposi sarcoma in 1 patient who was successfully treated with surgical excision and reduction of immunosuppression. CONCLUSION: EBV-associated PTLD is the most frequently encountered de novo malignancy after LT and is easily treatable by chemotherapy and reduction of immunosuppression.
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spelling pubmed-60810112018-09-21 De novo malignancies after liver transplantation: a single-center experience Hegab, Bassem Khalaf, Hatem Allam, Naglaa Azzam, Ayman Al Khail, Faisal Aba Al-hamoudi, Waleed Kamel, Yasser Al Bahili, Hamad Al Sofayan, Mohammed Al-Sebayel, Mohammed Ann Saudi Med Original Article BACKGROUND AND OBJECTIVES: The recipients of liver transplantation (LT) are subjected to lifelong immunosuppression with its many drawbacks. De novo and recurrent malignancy in transplant recipients are attributed to attenuation of immunosurveillance. In the present study, we present our experience with de novo malignancies encountered after both deceased and living donor liver transplantations. DESIGN AND SETTING: Retrospective study of patients referred to LT center between April 2001 and January 2010 PATIENTS AND METHODS: Various data were collected including type of malignancy and histopathologic features, immunosuppression regimen, and patient survival. RESULTS: Of 248 LT procedures performed in 238 patients (10 retransplants), 8 patients (3.4%) developed de novo post-LT malignancies. De novo malignancies included post-LT lymphoproliferative disorders (PTLD) in 5 patients who were all Epstein-Barr virus (EBV) positive, and who were treated successfully with anti-CD20 monoclonal antibody therapy, reduction of immunosuppression, and control of EBV activity; urinary bladder cancer in 1 patient who was treated with radical surgical resection and chemotherapy but died of bone and lung metastasis within 1 year of diagnosis; endometrial carcinoma in 1 patient who was treated with radical surgical resection; and Kaposi sarcoma in 1 patient who was successfully treated with surgical excision and reduction of immunosuppression. CONCLUSION: EBV-associated PTLD is the most frequently encountered de novo malignancy after LT and is easily treatable by chemotherapy and reduction of immunosuppression. King Faisal Specialist Hospital and Research Centre 2012 /pmc/articles/PMC6081011/ /pubmed/22705604 http://dx.doi.org/10.5144/0256-4947.2012.355 Text en Copyright © 2012, Annals of Saudi Medicine This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Hegab, Bassem
Khalaf, Hatem
Allam, Naglaa
Azzam, Ayman
Al Khail, Faisal Aba
Al-hamoudi, Waleed
Kamel, Yasser
Al Bahili, Hamad
Al Sofayan, Mohammed
Al-Sebayel, Mohammed
De novo malignancies after liver transplantation: a single-center experience
title De novo malignancies after liver transplantation: a single-center experience
title_full De novo malignancies after liver transplantation: a single-center experience
title_fullStr De novo malignancies after liver transplantation: a single-center experience
title_full_unstemmed De novo malignancies after liver transplantation: a single-center experience
title_short De novo malignancies after liver transplantation: a single-center experience
title_sort de novo malignancies after liver transplantation: a single-center experience
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081011/
https://www.ncbi.nlm.nih.gov/pubmed/22705604
http://dx.doi.org/10.5144/0256-4947.2012.355
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