Abd-el-Baki J, Stefanato C M, Koh H K, Demierre M F, Foss F M
Department of Dermatology, Boston University School of Medicine, Massachusetts, USA.
Oncology (Williston Park). 1998 Oct;12(10):1521-30; discussion 1532-4.
Cutaneous lymphomas comprise a spectrum of diseases characterized by infiltration of the skin by malignant lymphocytes. The clinical manifestations of cutaneous lymphomas vary, and they can mimic benign dermatoses, as well as nodal or visceral malignancies with cutaneous spread. Cutaneous lymphomas are divided into T-cell lymphomas and B-cell lymphomas. Cutaneous T-cell lymphomas include mycosis fungoides, Sézary syndrome, lymphomatoid papulosis, CD30+ large cell lymphoma, and adult T-cell leukemia/lymphoma. The extent and severity of skin manifestations in cutaneous T-cell lymphomas are prognostic indicators of extracutaneous involvement. Primary cutaneous B-cell lymphomas comprise 10% to 25% of all primary cutaneous non-Hodgkin's lymphomas and are classified according to their cell of origin. Most cutaneous B-cell lymphomas have an indolent course and excellent prognosis when compared to their nodal counterparts. Many factors have been implicated in the etiology of cutaneous lymphomas, including chemical and drug exposures, as well as microbial agents, such as the Epstein-Barr virus (EBV), human T-lymphocyte virus-1 (HTLV-1), and Borrelia burgdorferi. Immunohistochemistry and lymphocyte-receptor gene rearrangement studies are useful in distinguishing malignant from benign conditions.
皮肤淋巴瘤包括一系列以恶性淋巴细胞浸润皮肤为特征的疾病。皮肤淋巴瘤的临床表现各异,可酷似良性皮肤病,也可类似伴有皮肤播散的淋巴结或内脏恶性肿瘤。皮肤淋巴瘤分为T细胞淋巴瘤和B细胞淋巴瘤。皮肤T细胞淋巴瘤包括蕈样肉芽肿、 Sézary综合征、淋巴瘤样丘疹病、CD30 +大细胞淋巴瘤和成人T细胞白血病/淋巴瘤。皮肤T细胞淋巴瘤皮肤表现的范围和严重程度是皮肤外受累的预后指标。原发性皮肤B细胞淋巴瘤占所有原发性皮肤非霍奇金淋巴瘤的10%至25%,并根据其起源细胞进行分类。与淋巴结型B细胞淋巴瘤相比,大多数原发性皮肤B细胞淋巴瘤病程惰性,预后良好。皮肤淋巴瘤的病因涉及许多因素,包括化学物质和药物接触,以及微生物制剂,如爱泼斯坦-巴尔病毒(EBV)、人类T淋巴细胞病毒1型(HTLV-1)和伯氏疏螺旋体。免疫组织化学和淋巴细胞受体基因重排研究有助于区分恶性和良性病变。