Rendina G M, Donadio C, Fabri M, Orfei G, Rutigliano A, Saccucci P
Eur J Gynaecol Oncol. 1984;5(2):140-5.
The Authors report their experience in 24 cases of sarcoma of the corpus uteri observed between 1971 and 1981. After pointing out that their experiences confirm the extreme rareness of these neoplastic forms they dwell on diagnostic, prognostic and histologic criteria of classification and conclude that sarcomas of the corpus uteri - mostly leiomyosarcomas - of fibromatous origin - are always potentially very malignant with low 5-year survival rates despite combined treatment with surgery + radiotherapy + antiblastic therapy.
作者报告了他们在1971年至1981年间观察到的24例子宫体肉瘤的经验。在指出他们的经验证实了这些肿瘤形式极为罕见之后，他们详述了分类的诊断、预后和组织学标准，并得出结论：子宫体肉瘤——主要是平滑肌肉瘤——起源于纤维瘤，尽管采用手术+放疗+抗瘤治疗联合治疗，其5年生存率仍很低，始终具有潜在的高度恶性。
