Adult T-cell leukemia/lymphoma
Main Author: | |
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Publication Date: | 2016 |
Other Authors: | , |
Format: | Article |
Language: | eng |
Source: | Revista da Associação Médica Brasileira (Online) |
Download full: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302016000700691 |
Summary: | Summary Adult T-cell leukemia/lymphoma (ATL) is a malignancy of mature CD4+ T-cells caused by human T-cell lymphotropic virus type 1 (HTLV-1). Twenty million people are believed to be infected throughout the world, mostly in Japan, Africa, the Caribbean, and South America, particularly in Brazil and Peru. ATL affects about 5% of infected individuals and is classified in the following clinical forms: acute, lymphoma, primary cutaneous tumoral, chronic (favorable and unfavorable), and smoldering (leukemic and non-leukemic). Although it is considered an aggressive disease, there are cases with a long progression. We emphasize the importance of clinical classification as an indispensable element for evaluating prognosis and appropriate therapeutic approach. Since several cases have been published in Brazil and this disease is still poorly known, we decided to make a review paper for dissemination of clinical, hematological and pathological aspects, diagnosis, and therapy. The best way to reduce the occurrence of ATL would be halting the transmission of the virus through breastfeeding. |
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Adult T-cell leukemia/lymphomahuman T-cell lymphotropic virus 1adult T-cell leukemia/lymphomaT-cell lymphomaperipheral T-cell lymphomamycosis fungoidescutaneous T-cell lymphomaSummary Adult T-cell leukemia/lymphoma (ATL) is a malignancy of mature CD4+ T-cells caused by human T-cell lymphotropic virus type 1 (HTLV-1). Twenty million people are believed to be infected throughout the world, mostly in Japan, Africa, the Caribbean, and South America, particularly in Brazil and Peru. ATL affects about 5% of infected individuals and is classified in the following clinical forms: acute, lymphoma, primary cutaneous tumoral, chronic (favorable and unfavorable), and smoldering (leukemic and non-leukemic). Although it is considered an aggressive disease, there are cases with a long progression. We emphasize the importance of clinical classification as an indispensable element for evaluating prognosis and appropriate therapeutic approach. Since several cases have been published in Brazil and this disease is still poorly known, we decided to make a review paper for dissemination of clinical, hematological and pathological aspects, diagnosis, and therapy. The best way to reduce the occurrence of ATL would be halting the transmission of the virus through breastfeeding.Associação Médica Brasileira2016-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302016000700691Revista da Associação Médica Brasileira v.62 n.7 2016reponame:Revista da Associação Médica Brasileira (Online)instname:Associação Médica Brasileira (AMB)instacron:AMB10.1590/1806-9282.62.07.691info:eu-repo/semantics/openAccessOliveira,Pedro DantasFarre,LourdesBittencourt,Achiléa Lisboaeng2016-12-01T00:00:00Zoai:scielo:S0104-42302016000700691Revistahttps://ramb.amb.org.br/ultimas-edicoes/#https://old.scielo.br/oai/scielo-oai.php||ramb@amb.org.br1806-92820104-4230opendoar:2016-12-01T00:00Revista da Associação Médica Brasileira (Online) - Associação Médica Brasileira (AMB)false |
dc.title.none.fl_str_mv |
Adult T-cell leukemia/lymphoma |
title |
Adult T-cell leukemia/lymphoma |
spellingShingle |
Adult T-cell leukemia/lymphoma Oliveira,Pedro Dantas human T-cell lymphotropic virus 1 adult T-cell leukemia/lymphoma T-cell lymphoma peripheral T-cell lymphoma mycosis fungoides cutaneous T-cell lymphoma |
title_short |
Adult T-cell leukemia/lymphoma |
title_full |
Adult T-cell leukemia/lymphoma |
title_fullStr |
Adult T-cell leukemia/lymphoma |
title_full_unstemmed |
Adult T-cell leukemia/lymphoma |
title_sort |
Adult T-cell leukemia/lymphoma |
author |
Oliveira,Pedro Dantas |
author_facet |
Oliveira,Pedro Dantas Farre,Lourdes Bittencourt,Achiléa Lisboa |
author_role |
author |
author2 |
Farre,Lourdes Bittencourt,Achiléa Lisboa |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Oliveira,Pedro Dantas Farre,Lourdes Bittencourt,Achiléa Lisboa |
dc.subject.por.fl_str_mv |
human T-cell lymphotropic virus 1 adult T-cell leukemia/lymphoma T-cell lymphoma peripheral T-cell lymphoma mycosis fungoides cutaneous T-cell lymphoma |
topic |
human T-cell lymphotropic virus 1 adult T-cell leukemia/lymphoma T-cell lymphoma peripheral T-cell lymphoma mycosis fungoides cutaneous T-cell lymphoma |
description |
Summary Adult T-cell leukemia/lymphoma (ATL) is a malignancy of mature CD4+ T-cells caused by human T-cell lymphotropic virus type 1 (HTLV-1). Twenty million people are believed to be infected throughout the world, mostly in Japan, Africa, the Caribbean, and South America, particularly in Brazil and Peru. ATL affects about 5% of infected individuals and is classified in the following clinical forms: acute, lymphoma, primary cutaneous tumoral, chronic (favorable and unfavorable), and smoldering (leukemic and non-leukemic). Although it is considered an aggressive disease, there are cases with a long progression. We emphasize the importance of clinical classification as an indispensable element for evaluating prognosis and appropriate therapeutic approach. Since several cases have been published in Brazil and this disease is still poorly known, we decided to make a review paper for dissemination of clinical, hematological and pathological aspects, diagnosis, and therapy. The best way to reduce the occurrence of ATL would be halting the transmission of the virus through breastfeeding. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-10-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302016000700691 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302016000700691 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/1806-9282.62.07.691 |
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 |
Associação Médica Brasileira |
publisher.none.fl_str_mv |
Associação Médica Brasileira |
dc.source.none.fl_str_mv |
Revista da Associação Médica Brasileira v.62 n.7 2016 reponame:Revista da Associação Médica Brasileira (Online) instname:Associação Médica Brasileira (AMB) instacron:AMB |
instname_str |
Associação Médica Brasileira (AMB) |
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AMB |
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AMB |
reponame_str |
Revista da Associação Médica Brasileira (Online) |
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Revista da Associação Médica Brasileira (Online) |
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Revista da Associação Médica Brasileira (Online) - Associação Médica Brasileira (AMB) |
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||ramb@amb.org.br |
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