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Primary cutaneous smoldering adult T-cell leukemia/ lymphoma

机译:成人原发性皮肤阴燃性T细胞白血病/淋巴瘤

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HTLV-1 is a virus that is endemic in southwesternJapan and the Caribbean and has been implicatedin the development of ATLL. ATLL, which is anuncommon malignant condition of peripheralT-lymphocytes, is characterized by four clinicalsubtypes, which include acute, lymphomatous,chronic, and smoldering types, that are based onLDH levels, calcium levels, and extent of organinvolvement. We present a 52-year- old woman withpruritic patches with scale on the buttocks and withtender, hyperpigmented macules and papules oftwo-years duration. Histopathologic examinationwas suggestive of mycosis fungoides, laboratoryresults showed HTLV-I and II, and the patient wasdiagnosed with primary cutaneous ATLL. We reviewthe literature on HTLV-1 and ATLL and specifically theprognosis of cutaneous ATLL. The literature suggeststhat a diagnosis of ATLL should be considered amongpatients of Caribbean origin or other endemicareas with skin lesions that suggest a cutaneousT-cell lymphoma, with clinicopathologic features ofmycosis fungoides. Differentiation between ATLLand cutaneous T-cell lymphoma is imperative as theyhave different prognoses and treatment approaches.
机译:HTLV-1是在日本西南部和加勒比海地区流行的一种病毒,与ATLL的发展有关。 ATLL是外周T淋巴细胞的一种罕见恶性疾病,其特征在于四种临床亚型,包括急性,淋巴瘤,慢性和阴燃类型,这是基于LDH水平,钙水平和器官参与程度而定。我们介绍了一名52岁女性,其瘙痒斑块在臀部和鳞片上有鳞片,色素沉着,色素沉着的黄斑和丘疹持续两年。组织病理学检查提示为真菌病真菌,实验室检查结果显示为HTLV-I和II,并且该患者被诊断为原发性皮肤ATLL。我们回顾了有关HTLV-1和ATLL的文献,特别是皮肤ATLL的预后。文献提示,应在加勒比血源性或其他伴有皮肤病灶的地方病的患者中考虑ATLL的诊断,这些皮肤病灶提示皮肤T细胞淋巴瘤,并具有真菌病的临床病理特征。由于ATLL和皮肤T细胞淋巴瘤的预后和治疗方法不同,因此必须进行区分。

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