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隆突性皮肤纤维肉瘤:病例报告

Dermatofibrosarcoma protuberance: case reports.

作者信息

Asuquo M E, Umoh M S, Ebughe G

机构信息

Department of Surgery, University of Calabar Teaching Hospital, Calabar, Nigeria.

出版信息

Ann Afr Med. 2007 Jun;6(2):80-3. doi: 10.4103/1596-3519.55710.

Abstract

BACKGROUND

Dermatofibrosarcoma protuberance (DFSP) is a relatively uncommon soft tissue neoplasm with intermediate to low grade malignancy, rarely metastasizing to regional lymph node or distant site but with proclivity for local recurrence due to inadequate resection.

METHODS

We evaluated the clinical histories and treatment outcomes of five consecutive patients who had histologic diagnosis of DFSP in the University of Calabar Teaching Hospital between 2000 and 2004.

RESULTS

The five cases reported had histologic diagnosis, sought for after excision. The male:female ratio was 2:3 with an age range of 17-35 years (mean, 26.6 years). Two of the lesions involved the neck and the other three sites involved were the anterior chest wall, groin and proximal thigh. Three of the lesions were recurrent.

CONCLUSION

DFSP is an uncommon tumour, painless, cutaneous and multilobulated lesions should arouse the suspicion of this tumour. Early presentation, pre-operative histologic diagnosis and postoperative evaluation of resection margins would enhance the goal of ensuring adequate excision for improved outcome.

摘要

背景

隆突性皮肤纤维肉瘤(DFSP)是一种相对罕见的软组织肿瘤,恶性程度为中低级别,很少转移至区域淋巴结或远处部位,但因切除不彻底易局部复发。

方法

我们评估了2000年至2004年间在卡拉巴尔大学教学医院连续5例经组织学诊断为DFSP患者的临床病史和治疗结果。

结果

报告的5例病例均为切除后经组织学诊断。男女比例为2:3,年龄范围为17至35岁(平均26.6岁)。其中2例病变位于颈部,另外3个受累部位分别为前胸壁、腹股沟和大腿近端。3例病变为复发性。

结论

DFSP是一种罕见肿瘤,无痛性、皮肤性和多叶状病变应怀疑为此种肿瘤。早期就诊、术前组织学诊断以及术后切缘评估将有助于确保充分切除以改善预后这一目标的实现。

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