Nishio Jun, Nakayama Shizuhide
Section of Orthopaedic Surgery, Department of Medicine, Fukuoka Dental College, 2-15-1 Tamura, Sawara-ku, Fukuoka 814-0193, Japan.
Department of Orthopaedic Surgery, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan.
Diagnostics (Basel). 2023 Sep 22;13(19):3022. doi: 10.3390/diagnostics13193022.
Myxofibrosarcoma (MFS) is one of the most common adult soft tissue sarcomas, typically arising in the extremities. Histologically, MFS is classified into three grades: low, intermediate, and high. Histological grades correlate with distant metastases and tumor-associated mortality. The diagnosis of MFS is challenging due to a lack of well-characterized immunohistochemical markers. High-grade MFS displays highly complex karyotypes with multiple copy number alterations. Recent integrated genomic studies have shown the predominance of somatic copy number aberrations. However, the molecular pathogenesis of high-grade MFS remains poorly understood. The standard treatment for localized MFS is surgical resection. The systemic treatment options for advanced disease are limited. This review provides an updated overview of the clinical and imaging features, pathogenesis, histopathology, and treatment of high-grade MFS.
黏液纤维肉瘤(MFS)是最常见的成人软组织肉瘤之一,通常发生于四肢。在组织学上,MFS分为三个级别:低级别、中级别和高级别。组织学分级与远处转移及肿瘤相关死亡率相关。由于缺乏特征明确的免疫组化标志物,MFS的诊断具有挑战性。高级别MFS显示出具有多个拷贝数改变的高度复杂核型。最近的综合基因组研究表明体细胞拷贝数畸变占主导地位。然而,高级别MFS的分子发病机制仍知之甚少。局限性MFS的标准治疗方法是手术切除。晚期疾病的全身治疗选择有限。本综述提供了高级别MFS的临床和影像学特征、发病机制、组织病理学及治疗的最新概述。