Oner U Ulkü, Tokar Baran, Açikalin Mustafa Fuat, Ilhan Hüseyin, Tel Nilüfer
Osmangazi Universitesi Tip Fakültesi Patoloji Anabilim Dal, 26480, Eskişehir, Turkey.
J Pediatr Surg. 2002 Jan;37(1):127-9. doi: 10.1053/jpsu.2002.29447.
The occurrence of true extrarenal Wilms' tumor is extremely rare. The most frequently noted extrarenal sites are the retroperitoneal and inguinal regions. In the female genital tract, the occurrence of Wilms' tumor has been documented in the uterus, endocervix, and ovary in isolated case reports. In this article the authors describe a case of ovarian Wilms' tumor in a 3.5-year-old girl. Her abdominal ultrasound scan and computed tomography scan showed a solid mass with cystic components on the left lower quadrant. Total excision was performed with left salpingo-oophorectomy. There was no other mass and also no evidence of metastasis. To the best of the authors' knowledge, this patient is the first reported case of primary ovarian Wilms' tumor arising in childhood.
真正的肾外威尔姆斯瘤极为罕见。最常发现的肾外部位是腹膜后和腹股沟区域。在女性生殖道中，孤立病例报告记载了子宫、子宫颈和卵巢发生威尔姆斯瘤的情况。在本文中，作者描述了一名3.5岁女孩的卵巢威尔姆斯瘤病例。她的腹部超声扫描和计算机断层扫描显示左下腹有一个含囊性成分的实性肿块。行左侧输卵管卵巢切除术并完整切除肿块。未发现其他肿块，也没有转移迹象。据作者所知，该患者是首例报道的儿童期原发性卵巢威尔姆斯瘤病例。
