T cell cutaneous lymphoma panniculitis type – A clinical case

Bibliographic Details
Main Author: Antunes, Marisa
Publication Date: 2004
Other Authors: Grima, Bruno, Chaveiro, Alexandra, Fernandes, Cândida, Nunes, Albertina, Afonso, Ana, Gomes, Maria, Riso, Nuno, Riscado, Vaz
Format: Article
Language: por
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://revista.spmi.pt/index.php/rpmi/article/view/1768
Summary: T cell cutaneous lymphoma (T.C.C.L.), panniculitis type, is a rare malignancy of postthymic T cells. A clinical case of a twenty-three year old, female patient, with a five-year evolution of recurret subcutaneous nodules and, later on, hepatosplenomegaly and fever is presented. The diagnosis was only possible with repeated cutaneous byopsies and in late stage of the disease. The patient died following a fatal and rapid leukemia transformation of the lymphoma. Often, the histological aspects of the skin,in early stages of T.C.C.L., does not reveal malignant characteristics. The diagnosis is frequently delayed due to lack of symptoms and dubious hystology, contribuing to the late institution of therapy. The differential diagnosis of T.C.C.L. is established with cutaneous manifestations of autoimmune diseases and end-stage Blastic NK lymphoma, requiring sofisticated laboratorial techniques such as skin, bone marrow and peripheral blood immunophenotyping.
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spelling T cell cutaneous lymphoma panniculitis type – A clinical caseLinfoma subcutâneo de células T tipo paniculíte – A propósito de um caso clínicoLinfoma cutâneopaniculiteeritema nodosoSubcutaneous Lymphomapanniculitiserythema nodosumT cell cutaneous lymphoma (T.C.C.L.), panniculitis type, is a rare malignancy of postthymic T cells. A clinical case of a twenty-three year old, female patient, with a five-year evolution of recurret subcutaneous nodules and, later on, hepatosplenomegaly and fever is presented. The diagnosis was only possible with repeated cutaneous byopsies and in late stage of the disease. The patient died following a fatal and rapid leukemia transformation of the lymphoma. Often, the histological aspects of the skin,in early stages of T.C.C.L., does not reveal malignant characteristics. The diagnosis is frequently delayed due to lack of symptoms and dubious hystology, contribuing to the late institution of therapy. The differential diagnosis of T.C.C.L. is established with cutaneous manifestations of autoimmune diseases and end-stage Blastic NK lymphoma, requiring sofisticated laboratorial techniques such as skin, bone marrow and peripheral blood immunophenotyping.O linfoma subcutâneo de células T (L.S.C.T.) tipo paniculite é uma neoplasia rara de células T pós-tímicas. Apresentamos o caso clínico de uma doente que, durante cinco anos, manifestou episódios recorrentes de nódulos subcutâneos, desenvolvendo posteriormente hepatoesplenomegalia e febre. O diagnóstico só foi possível após biopsias cutâneas seriadas, já numa fase tardia da evolução da doença. A doente faleceu após transformação leucémica do linfoma de evolução rapidamente fatal. Frequentemente a histologia da pele nas fases iniciais do L.S.C.T. tipo paniculíte não evidencia aspectos de malignidade. Este facto e a ausência de sintomatologia acompanhante contribuem para que o diagnóstico seja tardio, reduzindo assim as possibilidades de sucesso terapêutico. O diagnóstico diferencial desta situação inclui inicialmente as doenças auto-imunes com manifestações cutâneo-mucosas e, na fase final, o linfoma blástico NK. A distinção desta última entidade requer a utilização de técnicas laboratoriais sofisticadas, como a imunofenotipagem da pele, da medula óssea e do sangue periférico.Sociedade Portuguesa de Medicina Interna2004-12-31info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://revista.spmi.pt/index.php/rpmi/article/view/1768Internal Medicine; Vol. 11 No. 4 (2004): Outubro/ Dezembro; 197-202Medicina Interna; Vol. 11 N.º 4 (2004): Outubro/ Dezembro; 197-2022183-99800872-671Xreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAPporhttps://revista.spmi.pt/index.php/rpmi/article/view/1768https://revista.spmi.pt/index.php/rpmi/article/view/1768/1228Antunes, MarisaGrima, BrunoChaveiro, AlexandraFernandes, CândidaNunes, AlbertinaAfonso, AnaGomes, MariaRiso, NunoRiscado, Vazinfo:eu-repo/semantics/openAccess2023-04-01T06:11:42Zoai:oai.revista.spmi.pt:article/1768Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T10:55:34.649861Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv T cell cutaneous lymphoma panniculitis type – A clinical case
Linfoma subcutâneo de células T tipo paniculíte – A propósito de um caso clínico
title T cell cutaneous lymphoma panniculitis type – A clinical case
spellingShingle T cell cutaneous lymphoma panniculitis type – A clinical case
Antunes, Marisa
Linfoma cutâneo
paniculite
eritema nodoso
Subcutaneous Lymphoma
panniculitis
erythema nodosum
title_short T cell cutaneous lymphoma panniculitis type – A clinical case
title_full T cell cutaneous lymphoma panniculitis type – A clinical case
title_fullStr T cell cutaneous lymphoma panniculitis type – A clinical case
title_full_unstemmed T cell cutaneous lymphoma panniculitis type – A clinical case
title_sort T cell cutaneous lymphoma panniculitis type – A clinical case
author Antunes, Marisa
author_facet Antunes, Marisa
Grima, Bruno
Chaveiro, Alexandra
Fernandes, Cândida
Nunes, Albertina
Afonso, Ana
Gomes, Maria
Riso, Nuno
Riscado, Vaz
author_role author
author2 Grima, Bruno
Chaveiro, Alexandra
Fernandes, Cândida
Nunes, Albertina
Afonso, Ana
Gomes, Maria
Riso, Nuno
Riscado, Vaz
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Antunes, Marisa
Grima, Bruno
Chaveiro, Alexandra
Fernandes, Cândida
Nunes, Albertina
Afonso, Ana
Gomes, Maria
Riso, Nuno
Riscado, Vaz
dc.subject.por.fl_str_mv Linfoma cutâneo
paniculite
eritema nodoso
Subcutaneous Lymphoma
panniculitis
erythema nodosum
topic Linfoma cutâneo
paniculite
eritema nodoso
Subcutaneous Lymphoma
panniculitis
erythema nodosum
description T cell cutaneous lymphoma (T.C.C.L.), panniculitis type, is a rare malignancy of postthymic T cells. A clinical case of a twenty-three year old, female patient, with a five-year evolution of recurret subcutaneous nodules and, later on, hepatosplenomegaly and fever is presented. The diagnosis was only possible with repeated cutaneous byopsies and in late stage of the disease. The patient died following a fatal and rapid leukemia transformation of the lymphoma. Often, the histological aspects of the skin,in early stages of T.C.C.L., does not reveal malignant characteristics. The diagnosis is frequently delayed due to lack of symptoms and dubious hystology, contribuing to the late institution of therapy. The differential diagnosis of T.C.C.L. is established with cutaneous manifestations of autoimmune diseases and end-stage Blastic NK lymphoma, requiring sofisticated laboratorial techniques such as skin, bone marrow and peripheral blood immunophenotyping.
publishDate 2004
dc.date.none.fl_str_mv 2004-12-31
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dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://revista.spmi.pt/index.php/rpmi/article/view/1768
https://revista.spmi.pt/index.php/rpmi/article/view/1768/1228
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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. 11 No. 4 (2004): Outubro/ Dezembro; 197-202
Medicina Interna; Vol. 11 N.º 4 (2004): Outubro/ Dezembro; 197-202
2183-9980
0872-671X
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