A challenging fibrosarcomatous variant of dermatofibrosarcoma protuberans of head and neck: a case report

Sharad S. Desai, Jaydeep N. Pol, Jayesh S. Khivasara, Dinshaw M. Hormuzdi, Rajwardhan A. Shinde, Prachi P. Goyal, Swapnil Kaushal
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Abstract

Dermatofibrosarcoma protuberans (DFSP) is an unusual tumour of soft tissue with local invasive property with high rate of recurrence after surgical treatment. DFSP is frequently seen on the trunk and proximal extremities, although a 10-15% cases accounts in head and neck region. Mainstay for success of surgery in DFSP remains complete removal of tumour with adequate surgical margins of approximately 3cms. In head neck region challenges associated with surgery may be inadequate surgical margins, poor functional and cosmetic outcomes. We present a case of a 35 years old male reported to our hospital with complaint of rapidly growing mass over right cheek and retroauricular region causing facial deformity. Incisional biopsy diagnosis was made DFSP. The patient underwent wide local excision of tumour followed by adjuvant radiotherapy. Final histopatholgy showed fibrosarcomatous transformation of DFSP. After 24 months of post-op follow up, patient recovery was satisfactory without any signs of recurrence. This case is presented for its rarity and it highlights the need for proper diagnosis and treatment plan.
头颈部隆突性皮肤纤维肉瘤的挑战性纤维肉瘤变体:1例报告
摘要隆突性皮肤纤维肉瘤(DFSP)是一种罕见的软组织肿瘤,具有局部侵袭性,术后复发率高。DFSP常见于躯干和近端肢体,但有10-15%的病例发生在头颈部。DFSP手术成功的主要因素是完全切除肿瘤,手术切缘约为3厘米。在头颈部区域,与手术相关的挑战可能是手术切缘不足,功能和美容效果差。我们提出一个病例35岁的男性报告到我们的医院,投诉迅速增长的肿块在右脸颊和耳后区域造成面部畸形。切口活检诊断为DFSP。患者行局部大范围肿瘤切除术,并行辅助放疗。最终组织病理学显示DFSP纤维肉瘤转化。术后随访24个月,患者恢复良好,无复发迹象。这个病例是罕见的,它强调了正确的诊断和治疗计划的必要性。
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