医学
平滑肌肉瘤
软组织肉瘤
放射科
经皮
骨盆
肉瘤
全身疗法
活检
总体生存率
软组织
外科
癌症
内科学
病理
乳腺癌
作者
Nicolás Devaud,Olga Vornicova,Albiruni R. Abdul Razak,Korosh Khalili,Elizabeth G. Demicco,Cristina Mitric,Marcus Q. Bernardini,Rebecca A. Gladdy
标识
DOI:10.1016/j.soc.2022.03.011
摘要
Leiomyosarcomas are soft tissue tumors that are derived from smooth muscle mainly in the pelvis and retroperitoneum. Percutaneous biopsy is paramount to confirm diagnosis. Imaging is necessary to complete clinical staging. Multimodal treatment should be directed by expert sarcoma multidisciplinary teams that see a critical volume of these rare tumors. Surgery is the mainstay of curative intent treatment; however due to its high metastatic progression, there may be a benefit for neoadjuvant systemic treatment. Adjuvant systemic treatment has no proven disease-free survival, and its main role is in the palliative setting to potentially prolong overall survival.
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