Lamping J D, Blythe J G
Hum Pathol. 1977 Sep;8(5):583-5. doi: 10.1016/s0046-8177(77)80117-2.
Although the first Brenner tumor was reported in 1898 by MacNaughton-Jones, it was not until 1907 that Fritz Brenner described the tumor that bears his name. Since then more than 500 cases have been reported with bilaterality ranging from 3.7 to 8.0 per cent. However, this percentage is probably high. The tumor was originally thought to arise from follicular epithelium. Several other etiologies of the Brenner tumor have been suggested, including celomic surface epithelium, Walthard rests, teratoma, urothelium, and rete ovarii. The majority of Brenner tumors are inert, but there have been reports suggesting endocrine activity. The question of malignant transformation of the Brenner tumor has gained attention since Von Numers described the first malignant Brenner tumor in 1945. The determination of malignancy of these tumors has been hampered by vague histologic criteria for malignancy. The confusion surrounding the histogenesis, hormonal capabilities, and malignant potential of the Brenner tumor has persisted. A case report of bilateral Brenner tumors of the ovaries is presented as well as a review of the literature with emphasis on the bilaterality of Brenner tumors.
尽管首例勃勒纳瘤于1898年由麦克诺顿 - 琼斯报道,但直到1907年弗里茨·勃勒纳才描述了以他名字命名的这种肿瘤。从那时起,已报道了500多例病例,双侧发生率在3.7%至8.0%之间。然而,这个百分比可能偏高。该肿瘤最初被认为起源于滤泡上皮。有人提出了勃勒纳瘤的其他几种病因,包括体腔表面上皮、瓦尔塔德残余、畸胎瘤、尿路上皮和卵巢网。大多数勃勒纳瘤是无活性的,但有报道表明其具有内分泌活性。自1945年冯·努默斯描述首例恶性勃勒纳瘤以来,勃勒纳瘤恶性转化的问题受到了关注。这些肿瘤恶性程度的判定因恶性的组织学标准不明确而受到阻碍。围绕勃勒纳瘤的组织发生、激素功能和恶性潜能的困惑一直存在。本文报告了一例双侧卵巢勃勒纳瘤病例,并对文献进行了综述,重点是勃勒纳瘤的双侧性。