Xie Chuan, Shen Yangmei
Department of Gynecology and Obstetrics, West China Second University Hospital, Sichuan University Chengdu, Sichuan, P. R. China.
Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education Chengdu, Sichuan, P. R. China.
Am J Cancer Res. 2025 Jul 25;15(7):3323-3329. doi: 10.62347/WEKR2445. eCollection 2025.
Dermatofibrosarcoma protuberans (DFSP) is a rare, superficial low - to intermediate-grade sarcoma that typically presents as an asymptomatic slow-growing indurated dermal plaque. Although DFSP has a relatively high local recurrence rate, distant metastasis is rare. DFSP primarily occurs on the trunk and extremities but is seldom reported in the vulva. Due to its rarity, the clinical characteristics, pathological diagnosis, prognosis, and optimal management of vulvar DFSP remain poorly characterized. We retrospectively analyzed vulvar DFSP cases from our institution (January 2010 - January 2023). Clinical data and follow-up were obtained from hospital records, and imaging studies were reviewed via the picture archiving and communication system. Seven patients were included, with a median symptom-onset age of 44.3 years (range, 27-73). Patients typically presented with firm, asymptomatic masses. The labia majora was most commonly affected (n = 6, 85.7%). Tumor size averaged 4.3 cm (range, 2.0-6.5). All patients underwent excisional biopsy followed by wide local excision; none received lymphadenectomy. Surgical margins were documented in six patients, with negative margins achieved in five after initial wide excision. Over a mean follow-up of 27.3 months (range, 12-54), one patient (14.3%) experienced local recurrence. No recurrence occurred in patients with negative margins. Vulvar DFSP predominantly affects young and middle-aged women, manifesting as vulvar masses of variable size. Wide local excision is the primary treatment. While vulvar DFSP has a propensity for local recurrence, widely negative margins appear protective. Long-term follow-up is recommended to monitor for recurrence.
隆突性皮肤纤维肉瘤(DFSP)是一种罕见的浅表性低级别至中级别肉瘤,通常表现为无症状的缓慢生长的硬结性皮肤斑块。尽管DFSP局部复发率相对较高,但远处转移罕见。DFSP主要发生于躯干和四肢,但外阴部报道较少。由于其罕见性,外阴DFSP的临床特征、病理诊断、预后及最佳治疗方法仍缺乏充分描述。我们回顾性分析了我院(2010年1月至2023年1月)的外阴DFSP病例。临床资料和随访信息来自医院记录,影像学检查通过图像存档和通信系统进行回顾。共纳入7例患者,症状出现的中位年龄为44.3岁(范围27 - 73岁)。患者通常表现为质地硬、无症状的肿块。大阴唇最常受累(n = 6,85.7%)。肿瘤平均大小为4.3 cm(范围2.0 - 6.5 cm)。所有患者均接受切除活检,随后行广泛局部切除;均未接受淋巴结清扫术。6例患者记录了手术切缘,5例在初次广泛切除后切缘阴性。平均随访27.3个月(范围12 - 54个月),1例患者(14.3%)出现局部复发。切缘阴性的患者未出现复发。外阴DFSP主要影响中青年女性,表现为大小不一的外阴肿块。广泛局部切除是主要治疗方法。虽然外阴DFSP有局部复发倾向,但切缘广泛阴性似乎具有保护作用。建议进行长期随访以监测复发情况。