Geographic diversity of adult T-cell leukemia/lymphoma in Brazil

Detalhes bibliográficos
Autor(a) principal: Oliveira, Maria S. Pombo de
Data de Publicação: 1999
Outros Autores: Loureiro, Paula, Bittencourt, Achiléa [UNIFESP], Chiattone, Carlos, Borducchi, Davimar Miranda Maciel [UNIFESP], Carvalho, Silvia Maia Farias de, Barbosa, Helenemarie S., Rios, Maria, Sill, Anne, Cleghorn, Farley, Blattner, William, Brazilian ATLL Study Grp
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/11600/44028
http://doi.org/10.1002/(SICI)1097-0215(19991029)83:3<291
Resumo: We describe 195 cases of adult T-cell leukemia/lymphoma (ATLL) reported to the national registry of T-cell malignancies in Brazil between 1994 and 1998. We compared the effect of demographic differences and clinical features of 150 consecutive ATLL cases in different regions of this diverse country. At diagnosis, the predominant clinical sub-type was the acute type (60%), followed by lymphoma (22%)(v) chronic (10%) and smoldering (8%) types. Although we expected that different sub-types would be present in different regions, on the basis of immunogenetic factors determined by ethnicity, we did not demonstrate these differences. There were no significant differences among ATLL subtypes by age or gender. No ethnic group predominated in the total population of patients, but significant differences were noted when examining ethnic distribution by region. Reflecting the general population distribution, white patients were seen more often in Sao Paulo and black patients in Bahia, than in other regions, In most regions, cases were equally distributed between blacks and mulattos, except in Pernambuco, where blacks were less frequent. The main clinical features were lymphadenopathy, skin lesions, hypercalcemia and hepatomegaly. Fourteen patients (9%) suffered from HTLV-I-associated myelopathy (HAM/TSP), either at diagnosis or during follow-up of ATLL. All cases but one had antibodies to HTLV-I, with concordant results with ELISA, WE and FCR analyses. For the antibody-negative case, pol and tax gene sequences were present in tumor cells when subjected to PCR analyses. The prognosis was generally poor, suggesting that the disease in Brazil behaves in similar fashion regardless of ethnic or geographical differences. (C) 1999 Wiley-Liss, Inc.
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spelling Oliveira, Maria S. Pombo deLoureiro, PaulaBittencourt, Achiléa [UNIFESP]Chiattone, CarlosBorducchi, Davimar Miranda Maciel [UNIFESP]Carvalho, Silvia Maia Farias deBarbosa, Helenemarie S.Rios, MariaSill, AnneCleghorn, FarleyBlattner, WilliamBrazilian ATLL Study GrpCanc HospHEMOPESch MedUniversidade Federal de São Paulo (UNIFESP)Med Sch Santa Casa da MisercordiaInst Estadual HematolNew York Blood CtrUniv Maryland2018-06-15T17:44:17Z2018-06-15T17:44:17Z1999-10-29International Journal Of Cancer. New York: Wiley-liss, v. 83, n. 3, p. 291-298, 1999.0020-7136http://repositorio.unifesp.br/11600/44028http://doi.org/10.1002/(SICI)1097-0215(19991029)83:3<29110.1002/(SICI)1097-0215(19991029)83:3<291WOS:000082887300001We describe 195 cases of adult T-cell leukemia/lymphoma (ATLL) reported to the national registry of T-cell malignancies in Brazil between 1994 and 1998. We compared the effect of demographic differences and clinical features of 150 consecutive ATLL cases in different regions of this diverse country. At diagnosis, the predominant clinical sub-type was the acute type (60%), followed by lymphoma (22%)(v) chronic (10%) and smoldering (8%) types. Although we expected that different sub-types would be present in different regions, on the basis of immunogenetic factors determined by ethnicity, we did not demonstrate these differences. There were no significant differences among ATLL subtypes by age or gender. No ethnic group predominated in the total population of patients, but significant differences were noted when examining ethnic distribution by region. Reflecting the general population distribution, white patients were seen more often in Sao Paulo and black patients in Bahia, than in other regions, In most regions, cases were equally distributed between blacks and mulattos, except in Pernambuco, where blacks were less frequent. The main clinical features were lymphadenopathy, skin lesions, hypercalcemia and hepatomegaly. Fourteen patients (9%) suffered from HTLV-I-associated myelopathy (HAM/TSP), either at diagnosis or during follow-up of ATLL. All cases but one had antibodies to HTLV-I, with concordant results with ELISA, WE and FCR analyses. For the antibody-negative case, pol and tax gene sequences were present in tumor cells when subjected to PCR analyses. The prognosis was generally poor, suggesting that the disease in Brazil behaves in similar fashion regardless of ethnic or geographical differences. (C) 1999 Wiley-Liss, Inc.Canc Hosp, Inst Nacl Canc, Cell Markers Lab, Rio De Janeiro, BrazilHEMOPE, Dept Hematol, Recife, PE, BrazilSch Med, Dept Pathol, Salvador, BA, BrazilUniv Fed Sao Paulo, Dept Hematol, Sao Paulo, BrazilMed Sch Santa Casa da Misercordia, Sao Paulo, BrazilInst Estadual Hematol, Immunol Lab, Rio De Janeiro, BrazilNew York Blood Ctr, New York, NY 10021 USAUniv Maryland, Inst Human Virol, Baltimore, MD 21201 USAUniv Fed Sao Paulo, Dept Hematol, Sao Paulo, BrazilWeb of Science291-298engWiley-BlackwellInternational Journal Of Cancerhttp://olabout.wiley.com/WileyCDA/Section/id-406071.htmlinfo:eu-repo/semantics/openAccessGeographic diversity of adult T-cell leukemia/lymphoma in Brazilinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlereponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/440282021-10-05 21:43:44.048metadata only accessoai:repositorio.unifesp.br:11600/44028Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:27:18.122026Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Geographic diversity of adult T-cell leukemia/lymphoma in Brazil
title Geographic diversity of adult T-cell leukemia/lymphoma in Brazil
spellingShingle Geographic diversity of adult T-cell leukemia/lymphoma in Brazil
Oliveira, Maria S. Pombo de
title_short Geographic diversity of adult T-cell leukemia/lymphoma in Brazil
title_full Geographic diversity of adult T-cell leukemia/lymphoma in Brazil
title_fullStr Geographic diversity of adult T-cell leukemia/lymphoma in Brazil
title_full_unstemmed Geographic diversity of adult T-cell leukemia/lymphoma in Brazil
title_sort Geographic diversity of adult T-cell leukemia/lymphoma in Brazil
author Oliveira, Maria S. Pombo de
author_facet Oliveira, Maria S. Pombo de
Loureiro, Paula
Bittencourt, Achiléa [UNIFESP]
Chiattone, Carlos
Borducchi, Davimar Miranda Maciel [UNIFESP]
Carvalho, Silvia Maia Farias de
Barbosa, Helenemarie S.
Rios, Maria
Sill, Anne
Cleghorn, Farley
Blattner, William
Brazilian ATLL Study Grp
author_role author
author2 Loureiro, Paula
Bittencourt, Achiléa [UNIFESP]
Chiattone, Carlos
Borducchi, Davimar Miranda Maciel [UNIFESP]
Carvalho, Silvia Maia Farias de
Barbosa, Helenemarie S.
Rios, Maria
Sill, Anne
Cleghorn, Farley
Blattner, William
Brazilian ATLL Study Grp
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.institution.none.fl_str_mv Canc Hosp
HEMOPE
Sch Med
Universidade Federal de São Paulo (UNIFESP)
Med Sch Santa Casa da Misercordia
Inst Estadual Hematol
New York Blood Ctr
Univ Maryland
dc.contributor.author.fl_str_mv Oliveira, Maria S. Pombo de
Loureiro, Paula
Bittencourt, Achiléa [UNIFESP]
Chiattone, Carlos
Borducchi, Davimar Miranda Maciel [UNIFESP]
Carvalho, Silvia Maia Farias de
Barbosa, Helenemarie S.
Rios, Maria
Sill, Anne
Cleghorn, Farley
Blattner, William
Brazilian ATLL Study Grp
description We describe 195 cases of adult T-cell leukemia/lymphoma (ATLL) reported to the national registry of T-cell malignancies in Brazil between 1994 and 1998. We compared the effect of demographic differences and clinical features of 150 consecutive ATLL cases in different regions of this diverse country. At diagnosis, the predominant clinical sub-type was the acute type (60%), followed by lymphoma (22%)(v) chronic (10%) and smoldering (8%) types. Although we expected that different sub-types would be present in different regions, on the basis of immunogenetic factors determined by ethnicity, we did not demonstrate these differences. There were no significant differences among ATLL subtypes by age or gender. No ethnic group predominated in the total population of patients, but significant differences were noted when examining ethnic distribution by region. Reflecting the general population distribution, white patients were seen more often in Sao Paulo and black patients in Bahia, than in other regions, In most regions, cases were equally distributed between blacks and mulattos, except in Pernambuco, where blacks were less frequent. The main clinical features were lymphadenopathy, skin lesions, hypercalcemia and hepatomegaly. Fourteen patients (9%) suffered from HTLV-I-associated myelopathy (HAM/TSP), either at diagnosis or during follow-up of ATLL. All cases but one had antibodies to HTLV-I, with concordant results with ELISA, WE and FCR analyses. For the antibody-negative case, pol and tax gene sequences were present in tumor cells when subjected to PCR analyses. The prognosis was generally poor, suggesting that the disease in Brazil behaves in similar fashion regardless of ethnic or geographical differences. (C) 1999 Wiley-Liss, Inc.
publishDate 1999
dc.date.issued.fl_str_mv 1999-10-29
dc.date.accessioned.fl_str_mv 2018-06-15T17:44:17Z
dc.date.available.fl_str_mv 2018-06-15T17:44:17Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv International Journal Of Cancer. New York: Wiley-liss, v. 83, n. 3, p. 291-298, 1999.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/11600/44028
http://doi.org/10.1002/(SICI)1097-0215(19991029)83:3<291
dc.identifier.issn.none.fl_str_mv 0020-7136
dc.identifier.doi.none.fl_str_mv 10.1002/(SICI)1097-0215(19991029)83:3<291
dc.identifier.wos.none.fl_str_mv WOS:000082887300001
identifier_str_mv International Journal Of Cancer. New York: Wiley-liss, v. 83, n. 3, p. 291-298, 1999.
0020-7136
10.1002/(SICI)1097-0215(19991029)83:3<291
WOS:000082887300001
url http://repositorio.unifesp.br/11600/44028
http://doi.org/10.1002/(SICI)1097-0215(19991029)83:3<291
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv International Journal Of Cancer
dc.rights.driver.fl_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 291-298
dc.publisher.none.fl_str_mv Wiley-Blackwell
publisher.none.fl_str_mv Wiley-Blackwell
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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