首页> 外文期刊>The Journal of dermatology >New entity, definition and diagnostic criteria of cutaneous adult T-cell leukemia/lymphoma: human T-lymphotropic virus type 1 proviral DNA load can distinguish between cutaneous and smoldering types.
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New entity, definition and diagnostic criteria of cutaneous adult T-cell leukemia/lymphoma: human T-lymphotropic virus type 1 proviral DNA load can distinguish between cutaneous and smoldering types.

机译:皮肤成人T细胞白血病/淋巴瘤的新实体,定义和诊断标准:人类T淋巴病毒1型原病毒DNA负荷可以区分皮肤和阴燃类型。

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摘要

Adult T-cell leukemia/lymphoma (ATLL) has been divided into four subtypes up to now: (i) acute; (ii) lymphoma; (iii) chronic; and (iv) smoldering. Skin lesion(s) may be present and the cases showing less than 5% abnormal T-lymphocytes in peripheral blood without involvement of other organs, have been classified as smoldering ATLL. However, this type of ATLL with skin manifestations had a worse prognosis than that without skin lesions. This study aimed to define and distinguish cutaneous ATLL lacking nodal lymphoma and leukemic change from smoldering ATLL. We propose an entity of cutaneous ATLL, which has less than 5% abnormal T lymphocyte in peripheral blood, a normal lymphocyte count (i.e. <4 x 10(9)/L), no hypercalcemia and lactate dehydrogenase values of up to 1.5 times the normal upper limit. At least one of the histologically proven skin lesions should be present accompanying monoclonal integration of human T-cell lymphotropic virus type 1 (HTLV-1) proviral DNA in the skin lesion. Blood samples were collected from 41 HTLV-1-infected patients, 21 asymptomatic carriers, 16 patients with cutaneous ATLL and four patients with smoldering ATLL. HTLV-1 proviral loads, soluble interleukin-2 receptors and other parameters were examined in each case. HTLV-1 proviral DNA loads in smoldering ATLL group are significantly higher than those in asymptomatic carrier and cutaneous ATLL group. Cutaneous ATLL may be a distinct entity that should be separated from smoldering ATLL clinically and virologically.
机译:迄今为止,成人T细胞白血病/淋巴瘤(ATLL)已分为四种亚型:(i)急性; (ii)淋巴瘤; (iii)慢性的; (iv)阴燃。可能存在皮肤病变,并且外周血中少于5%的异常T淋巴细胞出现异常而没有其他器官受累的病例已被分类为闷热的ATLL。然而,这种类型的具有皮肤表现的ATLL的预后要比没有皮肤病变的预后要差。这项研究旨在定义和区分没有淋巴瘤和白血病变化的皮肤ATLL和阴燃的ATLL。我们提出了一种皮肤ATLL实体,其外周血中异常T淋巴细胞少于5%,淋巴细胞计数正常(即<4 x 10(9)/ L),无高钙血症,乳酸脱氢酶值是其的1.5倍。正常上限。至少有一种经组织学证实的皮肤病灶伴随皮肤病灶中人类T细胞淋巴病毒1型(HTLV-1)原病毒DNA的单克隆整合。收集了41例HTLV-1感染患者,21例无症状携带者,16例皮肤ATLL患者和4例阴燃性ATLL患者的血样。每种情况下检查HTLV-1前病毒负荷,可溶性白介素2受体和其他参数。闷热的ATLL组的HTLV-1前病毒DNA负荷明显高于无症状携带者和皮肤ATLL组的HTLV-1前病毒DNA负荷。皮肤ATLL可能是一个独特的实体,应从临床和病毒学角度将其与阴燃ATLL分开。

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