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.
Arch Gynecol Obstet. 2010 Jun;281(6):1023-8. doi: 10.1007/s00404-009-1331-6. Epub 2009 Dec 23.
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.
We had experienced two cases of MMMT of the fallopian tube. The clinical features, pathologic findings, diagnosis, therapy, and outcome were reviewed.
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.
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.
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。
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。
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。
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。