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皮肤淋巴增生性浸润的处理。疑难病变。

Approach to lymphoproliferative infiltrates of the skin. The difficult lesions.

作者信息

Kempf W, Dummer R, Burg G

机构信息

Department of Dermatology, University Zurich, Switzerland.

出版信息

Am J Clin Pathol. 1999 Jan;111(1 Suppl 1):S84-93.

PMID:9894473
Abstract

Primary cutaneous lymphomas (CLs) are the second most common group of extranodal non-Hodgkin's lymphomas. Cutaneous T-cell lymphomas (CTCLs) account for 60% to 65% of all primary CLs, whereas 20% to 25% of CLs are of B-cell origin. Besides the most common and well-known forms of CL, such as mycosis fungoides and follicular B-cell lymphomas, there are some rare and unusual variants of CL that represent about 10% of lymphoproliferative skin infiltrates. Discussed in detail are T- and B-cell pseudolymphomas as simulators of CL, the group of parapsoriasis and early mycosis fungoides, circumscribed CTCL, such as pagetoid reticulosis and syringolymphoid hyperplasia, granulomatous variants of CTCL, the group of primary CD30+ CTCL and the controversies in the classification and some rare, but distinct cutaneous B-cell lymphomas. The final diagnosis in CL is based on a constellation of clinical, histopathologic, and molecular-biologic criteria.

摘要

原发性皮肤淋巴瘤(CLs)是结外非霍奇金淋巴瘤中第二常见的类型。皮肤T细胞淋巴瘤(CTCLs)占所有原发性CLs的60%至65%,而20%至25%的CLs起源于B细胞。除了CL最常见和广为人知的形式,如蕈样肉芽肿和滤泡性B细胞淋巴瘤外,还有一些罕见和不寻常的CL变异型,约占淋巴细胞增生性皮肤浸润的10%。详细讨论了作为CL模拟物的T细胞和B细胞假性淋巴瘤、副银屑病和早期蕈样肉芽肿组、局限性CTCL,如斑块状类网状细胞增生症和汗腺淋巴样增生、CTCL的肉芽肿变异型、原发性CD30 + CTCL组以及分类中的争议,还有一些罕见但独特的皮肤B细胞淋巴瘤。CL的最终诊断基于一系列临床、组织病理学和分子生物学标准。

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