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原发性皮肤间变性大细胞淋巴瘤。一例病例报告提示消退性非典型组织细胞增多症和淋巴瘤样丘疹病是其亚型。

Primary anaplastic large-cell lymphoma of the skin. A case report suggesting that regressing atypical histiocytosis and lymphomatoid papulosis are subsets.

作者信息

Yashiro N, Kitajima J, Kobayashi H, Fushida H, Nakagawa K, Furukawa M, Hamada T

机构信息

Department of Dermatology, Osaka City University Medical School, Japan.

出版信息

J Am Acad Dermatol. 1994 Feb;30(2 Pt 2):358-63. doi: 10.1016/s0190-9622(94)70040-0.

Abstract

A patient with primary anaplastic large-cell lymphoma of the skin with characteristic clinical findings is described. The diagnosis was made on the basis of histologic and immunohistochemical findings. The phenotype of the tumor cells was not determined, but rearrangement of the T-cell receptor beta gene indicated that the tumor was of T-cell lineage. Despite high-grade malignancy of the tumor cells, the patient unexpectedly had a benign clinical course. The findings in this case suggest that regressing atypical histiocytosis and lymphomatoid papulosis type A are subsets of anaplastic large-cell lymphoma.

摘要

本文描述了一名患有原发性皮肤间变性大细胞淋巴瘤且具有特征性临床表现的患者。诊断基于组织学和免疫组化结果。肿瘤细胞的表型未确定,但T细胞受体β基因重排表明肿瘤为T细胞谱系。尽管肿瘤细胞具有高度恶性,但该患者意外地呈现出良性临床病程。该病例的发现提示,消退性非典型组织细胞增生症和A型淋巴瘤样丘疹病是间变性大细胞淋巴瘤的亚型。

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