聚焦卵巢癌肉瘤:范围界定综述。

Martina Gauci, Jean Calleja-Agius
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引用次数: 0

摘要

卵巢癌肉瘤又称恶性混合性穆勒氏瘤,是一种不常见、侵袭性极强的恶性肿瘤,占所有卵巢肿瘤的1%至4%。它具有双相性,涉及恶性肉瘤细胞(间充质细胞)和癌细胞(上皮细胞)。它有多种亚型,如浆液性和子宫内膜样。不过,间质部分是肉瘤。约 90% 的卵巢癌肉瘤会扩散到卵巢外。卵巢癌肉瘤最被接受的两种起源学说是碰撞学说和转化学说。第三种理论是合并理论。即使仍局限于卵巢,预后仍然很差。在过去几年中,存活率没有任何变化。中位生存率低于 2 年。临床特征主要包括下腹痛和可触及的腹部肿块。人们对卵巢癌肉瘤的了解和研究仍然很少。卵巢癌肉瘤是一种罕见肿瘤,目前尚无详细的治疗共识。主要治疗方法包括细胞切除手术和化疗。化疗的类型、放疗的作用以及新型疗法都有待进一步研究。本文的主要目的是综述目前有关卵巢癌肉瘤的文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spotlight on Carcinosarcoma of the Ovary: A Scoping Review.

Ovarian carcinosarcoma, also referred as malignant mixed Mullerian tumour, is an uncommon, highly aggressive and malignant neoplasm which makes up 1 to 4% of all ovarian tumours. It is biphasic involving both malignant sarcomatous (mesenchymal) and carcinomatous (epithelial) cells. There are various subtypes such as serous and endometrioid. However, the mesenchymal part is sarcomatous. About 90% of cases of ovarian carcinosarcoma spread outside the ovary. The two most accepted theories of origin for carcinosarcoma of the ovary are the collision and conversion theories. A third theory is the combination theory. Prognosis remains poor even when still localised in the ovary. In the last few years, there has been no change in the survival rate. The median survival rate is lower than 2 years. Clinical features mainly include lower abdominal pain and a palpable abdominal mass. Ovarian carcinosarcoma remains poorly understood and understudied. Being a rare tumour, elaborate therapeutic consensus is not available for ovarian carcinosarcoma. The main treatment involves cytoreductive surgery and then chemotherapy. The type of chemotherapy, role of radiotherapy and novel therapies need to be further studied. The main objective of this article is to review the current literature on carcinosarcoma of the ovary.

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