医学
孤立性纤维性肿瘤
危险分层
血管外皮细胞瘤
软组织
软组织肉瘤
转移
放射科
病理
外科
内科学
癌症
遗传学
干细胞
川地34
生物
作者
Karineh Kazazian,Elizabeth G. Demicco,Marc de Perrot,D. Strauß,Carol J. Swallow
标识
DOI:10.1016/j.soc.2022.03.009
摘要
Solitary fibrous tumor (SFT) comprises a histologic spectrum of soft tissue neoplasms that are characterized by the unique NAB2-STAT6 gene fusion. Changes in diagnostic terminology and site-specific classification over the past few decades have resulted in a disjointed literature. Complete surgical excision with preservation of function remains the mainstay of treatment. New risk stratification systems including risk factors such as mitotic rate, age, tumor size, and presence of necrosis, among others, can be used to predict risk of recurrence or metastasis. Long-term follow-up after surgical resection is recommended. The clinical manifestations, diagnosis, management, and prognosis of SFT are reviewed here.
科研通智能强力驱动
Strongly Powered by AbleSci AI