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[隆突性皮肤纤维肉瘤的临床表现与病理]

[Clinical picture and pathology of dermatofibrosarcoma protuberans].

作者信息

Waldermann F, Hagedorn M

出版信息

Z Hautkr. 1985 Dec 1;60(23):1886-8, 1891-4.

PMID:4090578
Abstract

Dermatofibrosarcoma protuberans (D.p.) is a rare connective skin tumor (0.1%). On the basis of the literature and 13 own cases, we present data concerning age, sex, localisation, as well as clinical and histological findings. We report on pre-operative planning of treatment, surgical therapy (wide excision and closure by rotation flap), and clinical course. The follow-up indicates that D.p. is a neoplasia bearing a low rate of malignancy, which may change into a highly malignant tumor especially after treatment with radiation.

摘要

隆突性皮肤纤维肉瘤(D.p.)是一种罕见的皮肤结缔组织肿瘤(占0.1%)。基于文献资料及13例自身病例,我们给出了有关年龄、性别、肿瘤部位以及临床和组织学检查结果的数据。我们报告了术前治疗方案规划、手术治疗(广泛切除并用旋转皮瓣闭合创口)及临床病程。随访结果表明,隆突性皮肤纤维肉瘤是一种恶性程度较低的肿瘤,尤其是在接受放疗后,其可能转变为高恶性肿瘤。

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