隆突性皮肤纤维肉瘤:一个中心经验。

IF 0.8
Theodor Mareş, Laura Răducu, Adelaida Avino, Daniela-Elena Gheoca-Mutu, Răzvan Nicolae Teodoreanu, Cristian-Radu Jecan
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摘要

背景:隆突性皮肤纤维肉瘤(DFSP)是一种罕见的软组织肿瘤,被归类为非黑色素瘤皮肤癌。具有广泛安全范围的手术切除是治疗的基础,通常需要先进的重建方法来关闭伤口。本研究旨在报告我们连续治疗7例隆突性皮肤纤维肉瘤的经验。材料和方法:我们对2018年7月12日至2022年7月4日期间在罗马尼亚布加勒斯特临床急诊医院“Agrippa Ionescu教授”整形和重建外科住院的7例连续的皮肤纤维肉瘤隆突患者进行了回顾性研究。结果:患者平均年龄38.2岁。4例患者以广泛局部切除为主,3例患者来我院再次切除。所有病例均需要复杂的重建方法,其中3例采用裂厚皮肤移植物(STSG), 3例采用局部皮瓣,其中1例由于切除后缺损的较大,我们采用了局部推进皮瓣和STSG。2例组织病理诊断为纤维肉瘤分化(最大原发肿瘤尺寸),其中1例表现为筋膜侵犯,均行辅助放疗。结论:临床表现提示DFSP的软组织肿瘤,特别是在肿瘤体积增大的情况下,切口活检和随后的多学科方法将导致组织病理边缘阴性的广泛手术切除,作为低级别肉瘤的标准治疗方法,很少转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dermatofibrosarcoma Protuberans: One Centre Experience.

Background: Dermatofibrosarcoma protuberans (DFSP) is a rare soft tissue tumor that is classified as a non-melanoma skin cancer. Surgical excision with wide safety margins is the cornerstone treatment and frequently requires advanced reconstruction methods for wound closure. This study aimed to report our experience with the management of seven consecutive patients with dermatofibrosarcoma protuberans. Materials and Methods: We performed a retrospective study of seven consecutive patients with dermatofibrosarcoma protuberans admitted to our Plastic and Reconstructive Surgery Department of Clinical Emergency Hospital "Prof. Dr. Agrippa Ionescu" Bucharest, Romania, between July 12, 2018, and July 4, 2022. Results: The mean age of the patients was 38.2 years. In 4 patients, the primary treatment consisted of wide local excision, while 3 presented to our clinic for re-resection. All cases required complex reconstruction methods 3 patients with a split-thickness skin graft (STSG), 3 patients with local flaps, and in one patient, because of the superior size of the post-excisional defect, we used local advancement flaps and STSG. In two cases, the histopathological diagnosis revealed fibrosarcomatous differentiation (the largest primary tumor dimension), one of which showed fascial invasion, and both of them received adjuvant radiotherapy. Conclusion: A soft tissue tumor with a clinical appearance suggestive of DFSP, especially in cases of increased tumor sizes, incisional biopsy and subsequent multidisciplinary approach will lead to a wide surgical excision with negative histopathological margins, as a standard treatment, for a lowgrade sarcoma, which rarely metastasizes.

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