Lifschitz-Mercer B, Leider-Trejo L, Messer G, Peyser M R, Czernobilsky B
Institute of Pathology, Sourasky Medical Center, Tel Aviv, Israel.
Pathol Res Pract. 1998;194(3):183-7. doi: 10.1016/S0344-0338(98)80020-4.
The present report of a 25 year old woman with a primary ovarian angiosarcoma is supplemented by histochemical and ultrastructural studies and reviews the literature of this extremely rare neoplasm. Since this ovarian tumor, especially in young women, may constitute a diagnostic pitfall, problems relating to differential diagnosis are emphasized. Although the origin of this neoplasm appears to occur most likely from the rich ovarian vasculature, other less conventional histogenetic theories such as a possible origin in mixed mullerian tumor, in teratoma or in other ovarian germ cell tumors have also been proposed and are considered in this paper.
本文报告了一名25岁患有原发性卵巢血管肉瘤的女性病例，并辅以组织化学和超微结构研究，同时对这种极其罕见的肿瘤的文献进行了综述。由于这种卵巢肿瘤，尤其是在年轻女性中，可能构成诊断陷阱，因此强调了与鉴别诊断相关的问题。尽管这种肿瘤的起源似乎最有可能来自丰富的卵巢脉管系统，但也有人提出了其他不太传统的组织发生学理论，如可能起源于混合性苗勒管肿瘤、畸胎瘤或其他卵巢生殖细胞肿瘤，本文对此进行了探讨。
