Balasa R W, Adcock L L, Prem K A, Dehner L P
Obstet Gynecol. 1977 Jul;50(1):120-8.
The Brenner tumor of the ovary has been the topic of voluminous clinical and pathologic literature since its original description by Macnaughton-Jones in 1898. One of the major problems confronting most investigators of this uncommon neoplasm has been the question of histogenesis. There is general agreement that the tumor is derived from surface (coelomic) epithelium, as are the serous and mucinous cystadenomas. Most Brenner tumors are asymptomatic except for some which have features suggestive of estrogen production. The major pathologic variants are the proliferating and the malignant Brenner tumors; a poor prognosis is associated with the latter neoplasm. Approximately 30% of all benign Brenner tumors have a second histologic type of tumor in the ipsilateral or contralateral ovary, a serous or mucinous cystadenoma in most cases. Brenner tumors have also been reported in the broad ligament and in the testis on rare occasions.
自1898年麦克诺顿-琼斯首次描述卵巢布伦纳瘤以来,它一直是大量临床和病理学文献的主题。研究这种罕见肿瘤的大多数研究人员面临的主要问题之一是组织发生问题。人们普遍认为,该肿瘤与浆液性和黏液性囊腺瘤一样,起源于表面(体腔)上皮。除了一些具有提示雌激素产生特征的肿瘤外,大多数布伦纳瘤无症状。主要的病理变异型是增生性布伦纳瘤和恶性布伦纳瘤;后者预后较差。在所有良性布伦纳瘤中,约30%在同侧或对侧卵巢有第二种组织学类型的肿瘤,大多数情况下为浆液性或黏液性囊腺瘤。布伦纳瘤也有罕见报道发生于阔韧带和睾丸。