Angouridakis Nikolaos, Kafas Panagiotis, Jerjes Waseem, Triaridis Stefanos, Upile Tahwinder, Karkavelas Georgios, Nikolaou Angelos
Otorhinolaryngology, Head and Neck Surgery Department, AHEPA University Hospital, Thessaloniki, Greece.
Head Neck Oncol. 2011 Feb 4;3:5. doi: 10.1186/1758-3284-3-5.
Dermatofibrosarcoma protuberans (DFSP) is a rare cutaneous neoplasm associated with a high cure rate. We present a case of aggressive DFSP with fibrosarcomatous areas in the head and neck. A 28-year-old Mediterranean female presented with a 45-day history of rapidly growing cutaneous lesion of the face. Surgical biopsy confirmed the diagnosis of DFSP. Subsequently, the patient underwent wide local surgical resection, followed by reconstruction. Histopathology report revealed fibrosarcomatous transformation and the patient underwent adjuvant radiotherapy. The patient continues to be disease free at the 35-month follow-up.Although DFSP behave as non-aggressive malignancy, surgery with complete removal of the affected area is the intervention of choice. Moreover, adjuvant treatment and follow-up of the patient is essential in order to prevent recurrence.
隆突性皮肤纤维肉瘤(DFSP)是一种罕见的皮肤肿瘤,治愈率较高。我们报告一例发生于头颈部、伴有纤维肉瘤区域的侵袭性DFSP病例。一名28岁的地中海女性患者,面部出现迅速生长的皮肤病变,病程45天。手术活检确诊为DFSP。随后,患者接受了广泛的局部手术切除,接着进行了重建。组织病理学报告显示有纤维肉瘤样转化,患者接受了辅助放疗。在35个月的随访中,患者仍无疾病复发。尽管DFSP表现为非侵袭性恶性肿瘤,但手术彻底切除受累区域是首选的治疗方法。此外,对患者进行辅助治疗和随访对于预防复发至关重要。