枕中部巨大头皮隆突性皮纤维肉瘤1例。

Surgical neurology international Pub Date : 2024-11-15 eCollection Date: 2024-01-01 DOI:10.25259/SNI_604_2024
Muhammad Luqman Nul Hakim, Firman Priguna Tjahjono, Ahmad Faried
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引用次数: 0

摘要

背景:隆突性皮肤纤维肉瘤(DFSP)是一种罕见的皮肤癌,发生在皮肤的深层,最常见于躯干和四肢。由于其在文献中极为罕见,因此头皮上DFSP的表现值得记录。病例描述:我们描述了一个41岁的女性病例,她的后脑出现了一个逐渐增大的肿块。单发,大小19 × 12 × 10 cm,脓性分泌物,间歇性疼痛。计算机断层扫描显示枕骨中部一等密度肿块,未累及颅内。肿瘤切除及游离皮瓣与整形手术配合进行。患者于术后第7天出院,无任何神经功能缺损。结论:我们的病例是独特的,因为在没有任何辅助治疗的24个月后,没有任何复发,患者仍然很好。这是一种非常罕见的临床症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giant scalp dermatofibrosarcoma protuberans at mid-occipital scalp: A rare case report.

Background: Dermatofibrosarcoma protuberans (DFSP) is a rare type of skin cancer that arises in the deeper layers of the skin, most commonly on the trunk and limbs. The presentation of DFSP on the scalp is worth documentation due to its extremely rare occurrence in the literature.

Case description: We describe a case of a 41-year-old female presented with a lump on the back of the head with gradual enlargement. It was solitary with a size 19 × 12 × 10 cm with purulent discharge and intermittent pain. A computed tomography-scan showed an isodense mass at mid occipital without intracranial involvement. Tumor extirpation and the free flap were performed collaborated with plastic surgery. The patient was discharged unremarkably on the 7th postoperative day without any neurological deficits.

Conclusion: Our case is distinct because, after 24 months without any adjuvant therapy and without any recurrence, the patient is still doing well. This is a very rare clinical entity.

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