Pons J C, Benifla J L, N'Guebou F, Papiernik E, de la Fontaine P, Dazza F E, de Brux J
Service de Gynécologie-Obstétrique, Hôpital Antoine-Béclère, Clamart.
J Gynecol Obstet Biol Reprod (Paris). 1990;19(7):837-43.
This is a case report of a rare tumour of the ovary originally developing from the embryonal vestiges of the Wolffian duct and becoming a pure mesonephrotic carcinoma. Although initially considered to be benign, the course of the tumour is one of a potential low grade long term malignancy. Histological changes are of a pure mesonephrotic carcinoma or of a female adnexal tumour probably of wolffian origin (FATWO). It showed few specific traits. Each site of the development is constantly linked to the anatomy of the Wolffian duct. Metastases and recurrencies can develop late (after 5 to 10 years) following radical surgery. A survey of the literature confirmed the salient features of these tumours, which can differ from those of Müllerian origin.
这是一例罕见的卵巢肿瘤病例报告,该肿瘤最初起源于中肾管的胚胎遗迹,后发展为纯中肾样癌。尽管最初被认为是良性的,但肿瘤病程具有潜在的低级别长期恶性特征。组织学变化表现为纯中肾样癌或可能起源于中肾管的女性附件肿瘤(FATWO)。它几乎没有特异性特征。肿瘤的每个发生部位都与中肾管的解剖结构密切相关。根治性手术后,转移和复发可能在晚期(5至10年后)出现。文献综述证实了这些肿瘤的显著特征,它们可能与起源于苗勒管的肿瘤不同。