Fukuda Jun, Kumazawa Yukiyo, Fujimoto Toshio, Tanaka Toshinobu
Division of Obstetrics and Gynecology, Department of Reproductive and Developmental Medicine, Akita University School of Medicine, Akita, Japan.
J Obstet Gynaecol Res. 2010 Feb;36(1):191-4. doi: 10.1111/j.1447-0756.2009.01116.x.
A 50-year-old Japanese woman with Mayer-Rokitansky-Kustner-Hauser syndrome and two pelvic tumors underwent laparotomy. Laparotomy revealed that no torsion of the right ovarian tumor had occurred, with uterine leiomyoma originating from the right side of a rudimentary uterus. Histopathological examination demonstrated leiomyoma of the rudimentary uterus with positive staining for estrogen and progesterone receptors, and mucinous cyst adenoma of the right ovary. Uterine leiomyoma is rare in this syndrome and the present report represents the first published case complicated by ovarian tumor.
一名患有迈耶-罗基坦斯基-库斯特纳-豪泽综合征且有两个盆腔肿瘤的50岁日本女性接受了剖腹手术。剖腹手术显示右侧卵巢肿瘤未发生扭转，子宫平滑肌瘤起源于残角子宫右侧。组织病理学检查显示残角子宫平滑肌瘤雌激素和孕激素受体染色阳性，右侧卵巢为黏液性囊腺瘤。子宫平滑肌瘤在该综合征中较为罕见，本报告是首例并发卵巢肿瘤的病例报道。
