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隆突性皮肤纤维肉瘤复发?罕见病例。

Recurrence of a dermatofibrosarcoma protuberans? Rare case.

作者信息

Darraz Sohayb, Khattab Zakaria, Haichour Ilyesse, Mokhtari Omar, Farhaoui Amine El, Lachkar Adnane, Abdeljaouad Najib, Yacoubi Hicham

机构信息

Faculty of Medicine and Pharmacy, Mohammed I University, Oujda, Morocco.

Department of Traumatology, orthopedic Mohammed VI University Hospital Mohammed I University, Oujda, Morocco.

出版信息

Radiol Case Rep. 2024 Aug 5;19(10):4538-4543. doi: 10.1016/j.radcr.2024.06.096. eCollection 2024 Oct.

Abstract

Dermatofibrosarcoma protuberans (DFS) is a mesenchymal-origin skin tumor with intermediate malignancy. Though rare, it's not exceptional, comprising about 0.1% of malignant skin tumors. The authors discuss clinical, radiological, histopathological studies, and various therapeutic modalities for this tumor. Our 82-year-old patient presented with a 3 cm swelling on the right arm, initially undergoing biopsy followed by surgical excision of the mass. Adjuvant treatment with radiotherapy or chemotherapy is unnecessary unless recurrence or malignant transformation occurs. Histological analysis is crucial for diagnosis. The preferred treatment method is wide surgical excision. Prognosis primarily depends on malignancy, especially at the local level, with a high risk of recurrence. It's rare for a distinctly malignant sarcomatous transformation with metastasis to occur.

摘要

隆突性皮肤纤维肉瘤(DFS)是一种具有中度恶性的间叶组织起源的皮肤肿瘤。虽然罕见,但并不特殊,约占恶性皮肤肿瘤的0.1%。作者讨论了该肿瘤的临床、放射学、组织病理学研究以及各种治疗方式。我们82岁的患者右臂出现一个3厘米的肿块,最初进行了活检,随后对肿块进行了手术切除。除非发生复发或恶性转化,否则无需进行放疗或化疗的辅助治疗。组织学分析对诊断至关重要。首选的治疗方法是广泛手术切除。预后主要取决于恶性程度,尤其是局部恶性程度,复发风险高。发生明显恶性肉瘤样转化并伴有转移的情况很少见。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ac4/11357827/7aff82b540d0/gr1.jpg

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