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隆突性皮肤纤维肉瘤

[Dermatofibrosarcoma protuberans].

作者信息

Sanmartín O, Llombart B, López-Guerrero J A, Serra C, Requena C, Guillén C

机构信息

Servicio de Dermatología, Instituto Valenciano de Oncología, Valencia, España.

出版信息

Actas Dermosifiliogr. 2007 Mar;98(2):77-87. doi: 10.1016/s0001-7310(07)70019-4.

Abstract

Dermatofibrosarcoma protuberans (DFSP) is a soft tissue neoplasm of intermediate malignancy that is initially localized to the skin from where it can invade deep structures (fat, fascia, muscle and bone). It is the most frequent fibrohistiocytic tumor, comprising approximately 1.8 % of all soft tissue sarcomas and 0.1 % of all cancers. It has an estimated incidence of 0.8-5 cases per one million persons per year. Treatment of localized disease consists in complete surgical excision of the lesion by conventional surgery with wide margins (>3 cm) or by micrographic Mohs surgery. Although the cases of metastatic DFSP do not reach 5 % of the total, almost all of them appear after previous local relapses. The prognosis for metastatic cases is very poor with a survival of less than 2 years following detection of metastatic disease. Patients with locally advanced DFSP are not candidates for an initial radical surgical therapy therefore neoadyuvant treatment is required prior to surgery in order to reduce tumor burden. In this regard, chemotherapy and radiotherapy have not been highly efficacious so it is necessary to consider new alternatives. The demonstration of the oncogenic power of the translocation COL1A1-PDGFB in DFSP has allowed the successful introduction of drug therapy with antagonists of the PDGFB receptor for metastatic or locally advanced cases.

摘要

隆突性皮肤纤维肉瘤(DFSP)是一种中度恶性的软组织肿瘤,最初局限于皮肤,可由此侵犯深部结构(脂肪、筋膜、肌肉和骨骼)。它是最常见的纤维组织细胞肿瘤,约占所有软组织肉瘤的1.8%,占所有癌症的0.1%。其估计发病率为每年每100万人中有0.8 - 5例。局限性疾病的治疗包括通过常规手术广泛切除病变(切缘>3 cm)或通过显微外科莫氏手术完整切除病变。虽然转移性DFSP的病例不到总数的5%,但几乎所有这些病例都出现在先前局部复发之后。转移性病例的预后非常差,在检测到转移性疾病后生存期不到2年。局部晚期DFSP患者不适合进行初始根治性手术治疗,因此在手术前需要进行新辅助治疗以减轻肿瘤负荷。在这方面,化疗和放疗效果不佳,因此有必要考虑新的替代方案。DFSP中COL1A1 - PDGFB易位致癌作用的证实,使得针对转移性或局部晚期病例成功引入了使用PDGFB受体拮抗剂的药物治疗。

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