Suppr超能文献

输卵管恶性混合性米勒管瘤:两例报告并文献复习。

Malignant mixed müllerian tumor of the fallopian tube: report of two cases and review of literature.

机构信息

Department of Pathology, West China Second University Hospital, Sichuan University, No 20, Sect. 3, South People's Road, 610041, Chengdu, Sichuan, People's Republic of China.

出版信息

Arch Gynecol Obstet. 2010 Jun;281(6):1023-8. doi: 10.1007/s00404-009-1331-6. Epub 2009 Dec 23.

Abstract

PURPOSE

Malignant mixed müllerian tumors (MMMT) of the female genital tract is rare and it is extremely rare in the fallopian tube, with fewer than 53 cases reported in the literature.

METHODS

We had experienced two cases of MMMT of the fallopian tube. The clinical features, pathologic findings, diagnosis, therapy, and outcome were reviewed.

RESULTS

The clinical features and diagnosis were similar to those of primary carcinoma of the fallopian tube. Histologically, the two patients had homologous and heterologous elements mixed müllerian tumors. Treatment has focused on surgery with postoperative chemotherapy. Prognosis is poor, with fewer than half of patients surviving 2 years.

CONCLUSIONS

MMMT of fallopian tube is an uncommon carcinoma in the female genital tract. Cervical cytology and endometrial curettage could raise the suspicion of a tubal malignancy, but diagnosis is not usually made until the time of surgery. The patient survival will improve after surgery and postoperative chemotherapy.

摘要

目的

女性生殖道的恶性混合 Müllerian 肿瘤(MMMT)较为罕见,在输卵管中更为罕见,文献中报道的病例少于 53 例。

方法

我们曾遇到过两例输卵管 MMMT。回顾了其临床特征、病理发现、诊断、治疗和结局。

结果

临床特征和诊断与原发性输卵管癌相似。组织学上,两名患者均存在同源和异源混合 Müllerian 肿瘤。治疗侧重于手术联合术后化疗。预后较差,不到一半的患者存活 2 年以上。

结论

输卵管 MMMT 是女性生殖道中一种罕见的癌。宫颈细胞学和子宫内膜刮宫术可能会提示输卵管恶性肿瘤,但通常直到手术时才做出诊断。手术后和术后化疗可改善患者的生存。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验