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Four hepatosplenic T-cell lymphoma cases of Japanese patients.
Kawai, Hidetsugu; Matsushita, Hiromichi; Ohmachi, Ken; Kojima, Minoru; Machida, Shinichiro; Ogawa, Yoshiaki; Kawada, Hiroshi; Nakamura, Naoya; Ando, Kiyoshi.
Afiliação
  • Kawai H; Department of Hematology/Oncology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
  • Matsushita H; Department of Laboratory Medicine, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
  • Ohmachi K; Department of Hematology/Oncology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
  • Kojima M; Department of Hematology/Oncology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
  • Machida S; Department of Hematology/Oncology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
  • Ogawa Y; Department of Hematology/Oncology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
  • Kawada H; Department of Hematology/Oncology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
  • Nakamura N; Department of Pathology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
  • Ando K; Department of Hematology/Oncology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
Leuk Res Rep ; 5: 3-6, 2016.
Article em En | MEDLINE | ID: mdl-26870659
Hepatosplenic T-cell lymphoma (HSTCL), a rare type of γδ T-cell lymphoma, is characterized by hepatosplenomegaly and cytopenias. It is associated with immunodeficiency and its age of onset is reportedly between the 20s and 30s. We herein report 4 Japanese HSTCL cases. Three of them, including an elderly case that was 74 years of age, were not at adolescence. No cases had a history of immunodeficiency. All other disease phenotypes were similar to the typical HSTCL cases. These findings suggest that there are a certain proportion of HSTCL patients who presented after middle age.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Leuk Res Rep Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Japão País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Leuk Res Rep Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Japão País de publicação: Reino Unido