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由于 HTLV-1 引起的成人 T 细胞白血病/淋巴瘤的非典型表现:十二年持续性痒疹结节,随后出现急性小丘疹疹。

Atypical presentation of adult T-cell leukaemia/lymphoma due to HTLV-1: prurigo nodularis lasting twelve years followed by an acute micropapular eruption.

机构信息

Service de Dermatologie, Hôpital Saint-Louis, FR-75010 Paris, France.

出版信息

Acta Derm Venereol. 2010 May;90(3):287-90. doi: 10.2340/00015555-0846.

Abstract

Prurigo nodularis is a pruritic dermatosis of unknown origin. Human T-cell lymphotropic virus type 1 (HTLV-1) causes adult T-cell leukaemia/lymphoma. HTLV-1 is not considered to be a cause of prurigo nodularis. A 52-year-old black man, from the French West Indies, who had had prurigo nodularis for 12 years, presented with a distinct micropapular eruption with the typical pathological picture of epidermotropic T-cell lymphoma. Based on HTLV-1-positive serology and monoclonal integration of HTLV-1 we diagnosed smouldering adult T-cell leukaemia/lymphoma. Re-examination of previous skin biopsies revealed that the disease had been evolving for 12 years. Treatment with alpha-interferon, 3 x 106 units three times a week, associated with zidovudine, 1 g daily, resulted in complete remission within 4 months. When investigating a prurigo nodularis, we therefore recommend: (i) performing HTLV-1 serology if the patient comes from an endemic area; (ii) if positive, performing CD25 staining and looking for a HTLV-1 clonal integration; and (iii) if positive, using a treatment targeting HTLV-1.

摘要

结节性痒疹是一种病因不明的瘙痒性皮肤病。人类 T 细胞白血病病毒 1 型(HTLV-1)可引起成人 T 细胞白血病/淋巴瘤。HTLV-1 不被认为是结节性痒疹的病因。一名来自法属西印度群岛的 52 岁黑人男性,患有结节性痒疹 12 年,出现明显的丘疹性皮疹,具有表皮亲 T 细胞淋巴瘤的典型病理特征。基于 HTLV-1 阳性血清学和 HTLV-1 的单克隆整合,我们诊断为亚急性成人 T 细胞白血病/淋巴瘤。对先前皮肤活检的重新检查显示,该疾病已经发展了 12 年。用干扰素-α,每周 3 次,每次 3 x 106 单位,联合齐多夫定,每天 1 克,在 4 个月内完全缓解。因此,在调查结节性痒疹时,我们建议:(i)如果患者来自流行地区,则进行 HTLV-1 血清学检查;(ii)如果阳性,则进行 CD25 染色并寻找 HTLV-1 克隆整合;和(iii)如果阳性,则使用针对 HTLV-1 的治疗方法。

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