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Synovial Cell Sarcoma in an Adolescent Liver Transplant Recipient
Solid organ transplant recipients are at increased risk of malignancy. Pediatric transplant recipients particularly have a potentially higher risk given the young age of immunosuppression initiation. Posttransplant malignancies are the main cause of death in 5%–16% of liver transplantation patients....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658059/ https://www.ncbi.nlm.nih.gov/pubmed/31616756 http://dx.doi.org/10.14309/crj.0000000000000091 |
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author | Jaramillo, Catalina Gilani, Ahmed Haag, Mary Donaldson, Nathan Mack, Cara |
author_facet | Jaramillo, Catalina Gilani, Ahmed Haag, Mary Donaldson, Nathan Mack, Cara |
author_sort | Jaramillo, Catalina |
collection | PubMed |
description | Solid organ transplant recipients are at increased risk of malignancy. Pediatric transplant recipients particularly have a potentially higher risk given the young age of immunosuppression initiation. Posttransplant malignancies are the main cause of death in 5%–16% of liver transplantation patients. The frequency of de novo malignancies in pediatric liver transplant recipients has been reported to be 13%. Synovial sarcoma is a malignant mesenchymal neoplasm that has not been previously reported after liver transplantation. We report the case of an adolescent liver transplant recipient who was diagnosed with synovial sarcoma 14 years after liver transplantation. |
format | Online Article Text |
id | pubmed-6658059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-66580592019-10-15 Synovial Cell Sarcoma in an Adolescent Liver Transplant Recipient Jaramillo, Catalina Gilani, Ahmed Haag, Mary Donaldson, Nathan Mack, Cara ACG Case Rep J Case Report Solid organ transplant recipients are at increased risk of malignancy. Pediatric transplant recipients particularly have a potentially higher risk given the young age of immunosuppression initiation. Posttransplant malignancies are the main cause of death in 5%–16% of liver transplantation patients. The frequency of de novo malignancies in pediatric liver transplant recipients has been reported to be 13%. Synovial sarcoma is a malignant mesenchymal neoplasm that has not been previously reported after liver transplantation. We report the case of an adolescent liver transplant recipient who was diagnosed with synovial sarcoma 14 years after liver transplantation. Wolters Kluwer 2019-05-16 /pmc/articles/PMC6658059/ /pubmed/31616756 http://dx.doi.org/10.14309/crj.0000000000000091 Text en © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Case Report Jaramillo, Catalina Gilani, Ahmed Haag, Mary Donaldson, Nathan Mack, Cara Synovial Cell Sarcoma in an Adolescent Liver Transplant Recipient |
title | Synovial Cell Sarcoma in an Adolescent Liver Transplant Recipient |
title_full | Synovial Cell Sarcoma in an Adolescent Liver Transplant Recipient |
title_fullStr | Synovial Cell Sarcoma in an Adolescent Liver Transplant Recipient |
title_full_unstemmed | Synovial Cell Sarcoma in an Adolescent Liver Transplant Recipient |
title_short | Synovial Cell Sarcoma in an Adolescent Liver Transplant Recipient |
title_sort | synovial cell sarcoma in an adolescent liver transplant recipient |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658059/ https://www.ncbi.nlm.nih.gov/pubmed/31616756 http://dx.doi.org/10.14309/crj.0000000000000091 |
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