Cocciale M P, Plenat F, Reichert S, Modiano P, Barbaud A, Weber M, Schmutz J L
Service de Dermatologie, CHU Nancy.
Ann Dermatol Venereol. 1997;124(5):393-6.
Subcutaneous tissue is an uncommon primary localization for T-cell lymphomas. Panniculitis with recurrent papulonodules are reported in most cases.
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.
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.
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。
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。
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。
