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Posttransplant Lymphoproliferative Disorder in a Patient with Worsening Ascites after Liver Transplantation

Posttransplant lymphoproliferative disorder (PTLD) is a spectrum of diseases that involves abnormal lymphoid and/or plasmacytic proliferation in patients with solid organ or hematopoietic cell transplantation. It is a condition with a low incidence of 3.5–4.3% in liver transplant (LT) recipients. Th...

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Autores principales: Patel, Harsh D., Nevah Rubin, Moises I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611874/
https://www.ncbi.nlm.nih.gov/pubmed/29085683
http://dx.doi.org/10.1155/2017/7247438
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author Patel, Harsh D.
Nevah Rubin, Moises I.
author_facet Patel, Harsh D.
Nevah Rubin, Moises I.
author_sort Patel, Harsh D.
collection PubMed
description Posttransplant lymphoproliferative disorder (PTLD) is a spectrum of diseases that involves abnormal lymphoid and/or plasmacytic proliferation in patients with solid organ or hematopoietic cell transplantation. It is a condition with a low incidence of 3.5–4.3% in liver transplant (LT) recipients. This case involves a 63-year-old male with history of LT for chronic HCV induced cirrhosis who presented with abdominal distension related to worsening ascites. Cytological ascitic fluid analysis revealed EBV (+) malignant cells without a malignant focal point on imaging. Diagnosis of monomorphic PTLD with primary effusion lymphoma-like morphology and immunophenotype was established. This case highlights the complexity in diagnosis, different diagnostic modalities, and rare clinical presentations of PTLD.
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spelling pubmed-56118742017-10-30 Posttransplant Lymphoproliferative Disorder in a Patient with Worsening Ascites after Liver Transplantation Patel, Harsh D. Nevah Rubin, Moises I. Case Rep Hematol Case Report Posttransplant lymphoproliferative disorder (PTLD) is a spectrum of diseases that involves abnormal lymphoid and/or plasmacytic proliferation in patients with solid organ or hematopoietic cell transplantation. It is a condition with a low incidence of 3.5–4.3% in liver transplant (LT) recipients. This case involves a 63-year-old male with history of LT for chronic HCV induced cirrhosis who presented with abdominal distension related to worsening ascites. Cytological ascitic fluid analysis revealed EBV (+) malignant cells without a malignant focal point on imaging. Diagnosis of monomorphic PTLD with primary effusion lymphoma-like morphology and immunophenotype was established. This case highlights the complexity in diagnosis, different diagnostic modalities, and rare clinical presentations of PTLD. Hindawi 2017 2017-09-11 /pmc/articles/PMC5611874/ /pubmed/29085683 http://dx.doi.org/10.1155/2017/7247438 Text en Copyright © 2017 Harsh D. Patel and Moises I. Nevah Rubin. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Patel, Harsh D.
Nevah Rubin, Moises I.
Posttransplant Lymphoproliferative Disorder in a Patient with Worsening Ascites after Liver Transplantation
title Posttransplant Lymphoproliferative Disorder in a Patient with Worsening Ascites after Liver Transplantation
title_full Posttransplant Lymphoproliferative Disorder in a Patient with Worsening Ascites after Liver Transplantation
title_fullStr Posttransplant Lymphoproliferative Disorder in a Patient with Worsening Ascites after Liver Transplantation
title_full_unstemmed Posttransplant Lymphoproliferative Disorder in a Patient with Worsening Ascites after Liver Transplantation
title_short Posttransplant Lymphoproliferative Disorder in a Patient with Worsening Ascites after Liver Transplantation
title_sort posttransplant lymphoproliferative disorder in a patient with worsening ascites after liver transplantation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611874/
https://www.ncbi.nlm.nih.gov/pubmed/29085683
http://dx.doi.org/10.1155/2017/7247438
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