EBV-associated post-transplantation B-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression - a case report

<p>Abstract</p> <p>Epstein-Barr virus (EBV)-associated B-cell post-transplantation lymphoproliferative disorder (PTLD) is a severe complication following stem cell transplantation. This is believed to occur as a result of iatrogenic immunosuppression leading to a relaxation of T-ce...

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Main Authors: Niedobitek Gerald, Schmitz Nicole, Pönisch Wolfram, Moll Alexander, Krenauer Alexander, Niederwieser Dietger, Aigner Thomas
Format: Article
Language:English
Published: BMC 2010-03-01
Series:Diagnostic Pathology
Online Access:http://www.diagnosticpathology.org/content/5/1/21
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spelling doaj-1313c59310e34c7bb9ef1747cb0cf1d82020-11-25T00:20:59ZengBMCDiagnostic Pathology1746-15962010-03-01512110.1186/1746-1596-5-21EBV-associated post-transplantation B-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression - a case reportNiedobitek GeraldSchmitz NicolePönisch WolframMoll AlexanderKrenauer AlexanderNiederwieser DietgerAigner Thomas<p>Abstract</p> <p>Epstein-Barr virus (EBV)-associated B-cell post-transplantation lymphoproliferative disorder (PTLD) is a severe complication following stem cell transplantation. This is believed to occur as a result of iatrogenic immunosuppression leading to a relaxation of T-cell control of EBV infection and thus allowing viral reactivation and proliferation of EBV-infected B-lymphocytes. In support of this notion, reduction of immunosuppressive therapy may lead to regression of PTLD.</p> <p>We present a case of an 18-year-old male developing a monomorphic B-cell PTLD 2 months after receiving an allogenic stem cell transplant for acute lymphoblastic leukemia. Reduction of immunosuppressive therapy led to regression of lymphadenopathy. Nevertheless, the patient died 3 months afterwards due to extensive graft-vs.-host-disease and sepsis. As a diagnostic lymph node biopsy was performed only after reduction of immunosuppressive therapy, we are able to study the histopathological changes characterizing PTLD regression. We observed extensive apoptosis of blast cells, accompanied by an abundant infiltrate comprising predominantly CD8-positive, Granzyme B-positive T-cells. This observation supports the idea that regression of PTLD is mediated by cytotoxic T-cells and is in keeping with the observation that T-cell depletion, represents a major risk factor for the development of PTLD.</p> http://www.diagnosticpathology.org/content/5/1/21
collection DOAJ
language English
format Article
sources DOAJ
author Niedobitek Gerald
Schmitz Nicole
Pönisch Wolfram
Moll Alexander
Krenauer Alexander
Niederwieser Dietger
Aigner Thomas
spellingShingle Niedobitek Gerald
Schmitz Nicole
Pönisch Wolfram
Moll Alexander
Krenauer Alexander
Niederwieser Dietger
Aigner Thomas
EBV-associated post-transplantation B-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression - a case report
Diagnostic Pathology
author_facet Niedobitek Gerald
Schmitz Nicole
Pönisch Wolfram
Moll Alexander
Krenauer Alexander
Niederwieser Dietger
Aigner Thomas
author_sort Niedobitek Gerald
title EBV-associated post-transplantation B-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression - a case report
title_short EBV-associated post-transplantation B-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression - a case report
title_full EBV-associated post-transplantation B-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression - a case report
title_fullStr EBV-associated post-transplantation B-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression - a case report
title_full_unstemmed EBV-associated post-transplantation B-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression - a case report
title_sort ebv-associated post-transplantation b-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression - a case report
publisher BMC
series Diagnostic Pathology
issn 1746-1596
publishDate 2010-03-01
description <p>Abstract</p> <p>Epstein-Barr virus (EBV)-associated B-cell post-transplantation lymphoproliferative disorder (PTLD) is a severe complication following stem cell transplantation. This is believed to occur as a result of iatrogenic immunosuppression leading to a relaxation of T-cell control of EBV infection and thus allowing viral reactivation and proliferation of EBV-infected B-lymphocytes. In support of this notion, reduction of immunosuppressive therapy may lead to regression of PTLD.</p> <p>We present a case of an 18-year-old male developing a monomorphic B-cell PTLD 2 months after receiving an allogenic stem cell transplant for acute lymphoblastic leukemia. Reduction of immunosuppressive therapy led to regression of lymphadenopathy. Nevertheless, the patient died 3 months afterwards due to extensive graft-vs.-host-disease and sepsis. As a diagnostic lymph node biopsy was performed only after reduction of immunosuppressive therapy, we are able to study the histopathological changes characterizing PTLD regression. We observed extensive apoptosis of blast cells, accompanied by an abundant infiltrate comprising predominantly CD8-positive, Granzyme B-positive T-cells. This observation supports the idea that regression of PTLD is mediated by cytotoxic T-cells and is in keeping with the observation that T-cell depletion, represents a major risk factor for the development of PTLD.</p>
url http://www.diagnosticpathology.org/content/5/1/21
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