Post Transplant Lymphoproliferative Disease Isolated to Kidney Allograft

Detalhes bibliográficos
Autor(a) principal: Oliveira,Viviany Pontes de
Data de Publicação: 2022
Outros Autores: Esmeraldo,Ronaldo de Matos, Oliveira,Claudia Maria Costa de, Duarte,Fernando Barroso, Teixeira,André Costa, Sandes-Freitas,Tainá Veras de
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442022000100403
Resumo: ABSTRACT Post-transplantation lymphoproliferative disease (PTLD) comprises a heterogeneous group of hematolymphoid proliferations resulting from a monoclonal or polyclonal proliferation of lymphoid cells. The clinical presentation varies according to the affected sites. The gastrointestinal tract and the central nervous system are the most common, and constitutional symptoms are frequent. Isolated allograft involvement is rare. We report a case of polyclonal PTLD isolated in the kidney allograft in a patient who received an HLA-identical living donor seven years before. Noteworthy, this patient did not present constitutional symptoms, and his only clinical manifestation was graft dysfunction, expressed by an increase in serum creatinine and mild proteinuria. The diagnosis was performed through renal biopsy, which showed dense lymphoid interstitial infiltrate. The PTLD was polyclonal, unrelated to Epstein-Bar virus (EBV), and it was successfully treated with chemotherapy, reduced immunosuppression, and sirolimus.
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spelling Post Transplant Lymphoproliferative Disease Isolated to Kidney AllograftImmunossupressionKidney transplantationlymphomaABSTRACT Post-transplantation lymphoproliferative disease (PTLD) comprises a heterogeneous group of hematolymphoid proliferations resulting from a monoclonal or polyclonal proliferation of lymphoid cells. The clinical presentation varies according to the affected sites. The gastrointestinal tract and the central nervous system are the most common, and constitutional symptoms are frequent. Isolated allograft involvement is rare. We report a case of polyclonal PTLD isolated in the kidney allograft in a patient who received an HLA-identical living donor seven years before. Noteworthy, this patient did not present constitutional symptoms, and his only clinical manifestation was graft dysfunction, expressed by an increase in serum creatinine and mild proteinuria. The diagnosis was performed through renal biopsy, which showed dense lymphoid interstitial infiltrate. The PTLD was polyclonal, unrelated to Epstein-Bar virus (EBV), and it was successfully treated with chemotherapy, reduced immunosuppression, and sirolimus.Sociedade Brasileira de Patologia Clínica2022-01-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442022000100403Jornal Brasileiro de Patologia e Medicina Laboratorial v.58 2022reponame:Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)instname:Sociedade Brasileira de Patologia (SBP)instacron:SBP10.1900/jbpml.2022.58.446info:eu-repo/semantics/openAccessOliveira,Viviany Pontes deEsmeraldo,Ronaldo de MatosOliveira,Claudia Maria Costa deDuarte,Fernando BarrosoTeixeira,André CostaSandes-Freitas,Tainá Veras deeng2022-05-26T00:00:00Zoai:scielo:S1676-24442022000100403Revistahttp://www.scielo.br/jbpmlhttps://old.scielo.br/oai/scielo-oai.php||jbpml@sbpc.org.br1678-47741676-2444opendoar:2022-05-26T00:00Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) - Sociedade Brasileira de Patologia (SBP)false
dc.title.none.fl_str_mv Post Transplant Lymphoproliferative Disease Isolated to Kidney Allograft
title Post Transplant Lymphoproliferative Disease Isolated to Kidney Allograft
spellingShingle Post Transplant Lymphoproliferative Disease Isolated to Kidney Allograft
Oliveira,Viviany Pontes de
Immunossupression
Kidney transplantation
lymphoma
title_short Post Transplant Lymphoproliferative Disease Isolated to Kidney Allograft
title_full Post Transplant Lymphoproliferative Disease Isolated to Kidney Allograft
title_fullStr Post Transplant Lymphoproliferative Disease Isolated to Kidney Allograft
title_full_unstemmed Post Transplant Lymphoproliferative Disease Isolated to Kidney Allograft
title_sort Post Transplant Lymphoproliferative Disease Isolated to Kidney Allograft
author Oliveira,Viviany Pontes de
author_facet Oliveira,Viviany Pontes de
Esmeraldo,Ronaldo de Matos
Oliveira,Claudia Maria Costa de
Duarte,Fernando Barroso
Teixeira,André Costa
Sandes-Freitas,Tainá Veras de
author_role author
author2 Esmeraldo,Ronaldo de Matos
Oliveira,Claudia Maria Costa de
Duarte,Fernando Barroso
Teixeira,André Costa
Sandes-Freitas,Tainá Veras de
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Oliveira,Viviany Pontes de
Esmeraldo,Ronaldo de Matos
Oliveira,Claudia Maria Costa de
Duarte,Fernando Barroso
Teixeira,André Costa
Sandes-Freitas,Tainá Veras de
dc.subject.por.fl_str_mv Immunossupression
Kidney transplantation
lymphoma
topic Immunossupression
Kidney transplantation
lymphoma
description ABSTRACT Post-transplantation lymphoproliferative disease (PTLD) comprises a heterogeneous group of hematolymphoid proliferations resulting from a monoclonal or polyclonal proliferation of lymphoid cells. The clinical presentation varies according to the affected sites. The gastrointestinal tract and the central nervous system are the most common, and constitutional symptoms are frequent. Isolated allograft involvement is rare. We report a case of polyclonal PTLD isolated in the kidney allograft in a patient who received an HLA-identical living donor seven years before. Noteworthy, this patient did not present constitutional symptoms, and his only clinical manifestation was graft dysfunction, expressed by an increase in serum creatinine and mild proteinuria. The diagnosis was performed through renal biopsy, which showed dense lymphoid interstitial infiltrate. The PTLD was polyclonal, unrelated to Epstein-Bar virus (EBV), and it was successfully treated with chemotherapy, reduced immunosuppression, and sirolimus.
publishDate 2022
dc.date.none.fl_str_mv 2022-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1900/jbpml.2022.58.446
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dc.publisher.none.fl_str_mv
Sociedade Brasileira de Patologia Clínica
publisher.none.fl_str_mv
Sociedade Brasileira de Patologia Clínica
dc.source.none.fl_str_mv Jornal Brasileiro de Patologia e Medicina Laboratorial v.58 2022
reponame:Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)
instname:Sociedade Brasileira de Patologia (SBP)
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reponame_str Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)
collection Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)
repository.name.fl_str_mv Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) - Sociedade Brasileira de Patologia (SBP)
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