Post Transplant Lymphoproliferative Disease Isolated to Kidney Allograft
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , |
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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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 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
report |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442022000100403 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442022000100403 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1900/jbpml.2022.58.446 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
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) instacron:SBP |
instname_str |
Sociedade Brasileira de Patologia (SBP) |
instacron_str |
SBP |
institution |
SBP |
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) |
repository.mail.fl_str_mv |
||jbpml@sbpc.org.br |
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1752122297927335936 |