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[慢性硬皮病样综合征揭示皮下T细胞淋巴瘤]

[Chronic sclerodermiform syndrome disclosing subcutaneous T-cell lymphoma].

作者信息

Cocciale M P, Plenat F, Reichert S, Modiano P, Barbaud A, Weber M, Schmutz J L

机构信息

Service de Dermatologie, CHU Nancy.

出版信息

Ann Dermatol Venereol. 1997;124(5):393-6.

PMID:9739897
Abstract

INTRODUCTION

Subcutaneous tissue is an uncommon primary localization for T-cell lymphomas. Panniculitis with recurrent papulonodules are reported in most cases.

CASE REPORT

We report a case in which small-cell pleiomorphic non-Hodgkin lymphoma developed initially in subcutaneous tissue followed by secondary systemic extension. The first clinical manifestation was a sclerodermiform syndrome involving the four limbs.

DISCUSSION

This type of lymphoma appears to have a polymorphic clinical presentation. Physicians should be aware of this type of lymphoma and use immunohistological techniques for early diagnosis.

摘要

引言

皮下组织是T细胞淋巴瘤不常见的原发部位。大多数病例报告有伴有复发性丘疹结节的脂膜炎。

病例报告

我们报告一例小细胞多形性非霍奇金淋巴瘤最初发生于皮下组织,随后出现继发性全身播散。首发临床表现为累及四肢的硬皮病样综合征。

讨论

这种类型的淋巴瘤似乎具有多形性临床表现。医生应了解这种类型的淋巴瘤,并采用免疫组织学技术进行早期诊断。

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