A case series of adult T-cell leukemia-lymphoma, associated with human T-cell leukemia virus type-1, at a single center in a non-viral-endemic metropolitan area
Autor: | Kunihiro Tsukasaki, Mika Kohri, Yu Akuzawa, Nobutaka Kawai, Naoki Takahashi, Norio Asou, Daisuke Okamura, Tomoya Maeda, Akira Matsuda, Tsuyoshi Saeki, Maho Ishikawa |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
non-viral-endemic metropolitan area Male medicine.medical_specialty Referral medicine.medical_treatment Hematopoietic stem cell transplantation Single Center Adult T-cell leukemia/lymphoma Disease-Free Survival human T-cell leukemia virus type I (HTLV-1) 03 medical and health sciences 0302 clinical medicine Adult T-cell leukemia-lymphoma (ATL) immune system diseases Internal medicine hemic and lymphatic diseases Antineoplastic Combined Chemotherapy Protocols medicine metropolitan region Humans Leukemia-Lymphoma Adult T-Cell Aged Aged 80 and over Human T-lymphotropic virus 1 Performance status business.industry Hematopoietic Stem Cell Transplantation Combination chemotherapy General Medicine Middle Aged medicine.disease Allografts Lymphoma Survival Rate Leukemia 030104 developmental biology 030220 oncology & carcinogenesis Original Article Female business |
Zdroj: | Journal of Clinical and Experimental Hematopathology : JCEH |
ISSN: | 1880-9952 1346-4280 |
Popis: | We examined 13 patients with adult T-cell leukemia-lymphoma (ATL) diagnosed between 2007 and 2018 at a single center in a metropolitan area non-endemic for human T-cell leukemia virus type I (HTLV-1). The median age of the patients (eight male, five female) was 65 years (range, 48-83). The time from onset of symptoms to referral to our center was relatively short (median, 2 months; range, 1-9 months). Upon referral, all patients were suspected to have lymphoma, five were examined for soluble IL-2 receptor and two were examined for anti-HTLV-1 antibody. In ten of the 13 (77%), the patient themselves or their relatives were born in Kyushu. The birth places of the remaining three patients were unknown. Three patients (23%) had family histories of lymphoma. They all exhibited aggressive ATL (five acute, eight lymphoma type); however, the disease status was generally stable, with relatively stable performance status and low scores for prognostic indices. After combination chemotherapy, eight (62%) achieved remission. However, long-term remission was achieved in only one patient with localized lymphoma-type ATL and one young patient after allogeneic hematopoietic stem cell transplantation. In conclusion, at a center in a metropolitan and HTLV-1 non-endemic area in Japan, patients with ATL were relatively young and mainly presented with aggressive subtypes. At initial referral to our center, all 13 patients were suspected of having lymphoma but only two of having ATL. For centers in similar areas of Japan, prompt diagnosis and appropriate treatment of ATL patients will become increasingly necessary following the recent migration of HTLV-1 carriers to non-endemic areas. |
Databáze: | OpenAIRE |
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