Mantle cell lymphoma
Autor(a) principal: | |
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Data de Publicação: | 1999 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://revista.spmi.pt/index.php/rpmi/article/view/2031 |
Resumo: | ln the last years, newly lymphoid neoplasms werw recognized with clinical, morphologic and immunophenotypic characteristics distinct from the common forms described in the Working Formulation. One of the newly variant oflymphoma recently recognized were the mantle cell lymphoma in 1992. Case report: the authors reporta case of 73-year old man admitted in our deparrtment with symptomatic anemia, poor performance status, generalized lymphadenopathy, splenomegaly and lymphocitosis in the blood peripherial. He presented a elevated lactate dehydrogenase and b2 microglobulin levels. After evaluation of disease, that included bone marrow biopsy, immunophenotypic stdies of blood marrow, lymph node biopsy, chest-abdomen-pelvic computed tomographic scan, we made the diagnosis of diffuse mantle cell lymphoma, stage IV of Ann Arbor staging classification. made a gastrointestinal endoscopy that revealed multiple nodules in stmach and duodenal bulb which histologic findings shows a diffuse envolvement by lymphomatous B cells. The patient was treated until now, with four cycles of cyclophosphamide, vincristine, mitoxantrone and prednisone with partial remission after reavaluation. We review the literature about this subject. |
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Mantle cell lymphomaLinfoma de células do mantolinfoma de células do mantoestudos imunofenotípicosterapêuticamantle cell lymphomaimmunophenotipic studiestherapyln the last years, newly lymphoid neoplasms werw recognized with clinical, morphologic and immunophenotypic characteristics distinct from the common forms described in the Working Formulation. One of the newly variant oflymphoma recently recognized were the mantle cell lymphoma in 1992. Case report: the authors reporta case of 73-year old man admitted in our deparrtment with symptomatic anemia, poor performance status, generalized lymphadenopathy, splenomegaly and lymphocitosis in the blood peripherial. He presented a elevated lactate dehydrogenase and b2 microglobulin levels. After evaluation of disease, that included bone marrow biopsy, immunophenotypic stdies of blood marrow, lymph node biopsy, chest-abdomen-pelvic computed tomographic scan, we made the diagnosis of diffuse mantle cell lymphoma, stage IV of Ann Arbor staging classification. made a gastrointestinal endoscopy that revealed multiple nodules in stmach and duodenal bulb which histologic findings shows a diffuse envolvement by lymphomatous B cells. The patient was treated until now, with four cycles of cyclophosphamide, vincristine, mitoxantrone and prednisone with partial remission after reavaluation. We review the literature about this subject.Nos últimos anos, têm sido identificadas novas neoplasias linfóides com características clínicas, morfológicas e imunofenotípicas distintas das descritas pela Working Formulation. O linfoma de células do manto é uma variante do linfoma não Hodgkin descrito desde 1992. Os autores descrevem o caso de um homem de 72 anos internado no nosso hospital por anemia, mau estado geral, adenopatias generalizadas, esplenomegália e linfocitose no sangue periférico. A avaliação analítica inicial revelou uma desidrogenase láctica de 1487UIL e uma b2- microglobulina de 9.4mg/L. Após avaliação que incluiu biópsia óssea, mielograma, estudo imunofenotípico do sangue medular, biópsia ganglionar, tomografia axial computorizada toraco abdomino-pélvica chegou-se ao diagnóstico de linfoma de células do manto, estadio IV do sistema de classificação de Ann Arbor. A endoscopia digestiva alta revelou a presença de múltiplas lesões nodulares no estomago e bulbo duodenal cujos achados histológicos revelaram um envolvimento difuso por células B linfomatosas. O doente fez até agora 4 ciclos de quimioterapia com ciclofosfamida, vincristina, mitoxantrona e prednisona com remissão parcial após reavaliação. Os autores fizeram a propósito deste caso clínico uma revisão da literatura sobre linfoma de células do manto.Sociedade Portuguesa de Medicina Interna1999-03-31info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://revista.spmi.pt/index.php/rpmi/article/view/2031Internal Medicine; Vol. 6 No. 1 (1999): Janeiro/ Março; 18-22Medicina Interna; Vol. 6 N.º 1 (1999): Janeiro/ Março; 18-222183-99800872-671Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://revista.spmi.pt/index.php/rpmi/article/view/2031https://revista.spmi.pt/index.php/rpmi/article/view/2031/1425Oliveira, AnabelaDutschaman , Luísinfo:eu-repo/semantics/openAccess2023-07-01T06:11:21Zoai:oai.revista.spmi.pt:article/2031Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:02:06.983166Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Mantle cell lymphoma Linfoma de células do manto |
title |
Mantle cell lymphoma |
spellingShingle |
Mantle cell lymphoma Oliveira, Anabela linfoma de células do manto estudos imunofenotípicos terapêutica mantle cell lymphoma immunophenotipic studies therapy |
title_short |
Mantle cell lymphoma |
title_full |
Mantle cell lymphoma |
title_fullStr |
Mantle cell lymphoma |
title_full_unstemmed |
Mantle cell lymphoma |
title_sort |
Mantle cell lymphoma |
author |
Oliveira, Anabela |
author_facet |
Oliveira, Anabela Dutschaman , Luís |
author_role |
author |
author2 |
Dutschaman , Luís |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Oliveira, Anabela Dutschaman , Luís |
dc.subject.por.fl_str_mv |
linfoma de células do manto estudos imunofenotípicos terapêutica mantle cell lymphoma immunophenotipic studies therapy |
topic |
linfoma de células do manto estudos imunofenotípicos terapêutica mantle cell lymphoma immunophenotipic studies therapy |
description |
ln the last years, newly lymphoid neoplasms werw recognized with clinical, morphologic and immunophenotypic characteristics distinct from the common forms described in the Working Formulation. One of the newly variant oflymphoma recently recognized were the mantle cell lymphoma in 1992. Case report: the authors reporta case of 73-year old man admitted in our deparrtment with symptomatic anemia, poor performance status, generalized lymphadenopathy, splenomegaly and lymphocitosis in the blood peripherial. He presented a elevated lactate dehydrogenase and b2 microglobulin levels. After evaluation of disease, that included bone marrow biopsy, immunophenotypic stdies of blood marrow, lymph node biopsy, chest-abdomen-pelvic computed tomographic scan, we made the diagnosis of diffuse mantle cell lymphoma, stage IV of Ann Arbor staging classification. made a gastrointestinal endoscopy that revealed multiple nodules in stmach and duodenal bulb which histologic findings shows a diffuse envolvement by lymphomatous B cells. The patient was treated until now, with four cycles of cyclophosphamide, vincristine, mitoxantrone and prednisone with partial remission after reavaluation. We review the literature about this subject. |
publishDate |
1999 |
dc.date.none.fl_str_mv |
1999-03-31 |
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.uri.fl_str_mv |
https://revista.spmi.pt/index.php/rpmi/article/view/2031 |
url |
https://revista.spmi.pt/index.php/rpmi/article/view/2031 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://revista.spmi.pt/index.php/rpmi/article/view/2031 https://revista.spmi.pt/index.php/rpmi/article/view/2031/1425 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Sociedade Portuguesa de Medicina Interna |
publisher.none.fl_str_mv |
Sociedade Portuguesa de Medicina Interna |
dc.source.none.fl_str_mv |
Internal Medicine; Vol. 6 No. 1 (1999): Janeiro/ Março; 18-22 Medicina Interna; Vol. 6 N.º 1 (1999): Janeiro/ Março; 18-22 2183-9980 0872-671X reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799131687495401472 |