Kourda N, Elloumi H, Chérif K, Ben Jilani S, Zermani R
Service d'anatomie et cytologie pathologiques, hôpital Charles-Nicolle, boulevard 9-Avril, 1006 Tunis, Tunisia.
Gynecol Obstet Fertil. 2008 Mar;36(3):292-5. doi: 10.1016/j.gyobfe.2007.11.021. Epub 2008 Mar 5.
Brenner tumors account for only 1 to 2% of ovarian tumors. Proliferating Brenner tumors are characterized by an epithelial proliferation, resembling superficial well-differentiated urothelial carcinomas. A single 29-year-old patient was operated for an ovarian tumor. On gross examination, the tumor, which originated in the left ovary, was cystic multilocular and presented polyoid excrescences. Definitive histological exam showed a papillary proliferation lined by transitional cells without stroma infiltration. Mucinous cells lined some cavities. The diagnosis of proliferating Brenner tumor was made. Clinical and pathological characteristics of this rare entity will be discussed.
勃勒纳瘤仅占卵巢肿瘤的1%至2%。增殖性勃勒纳瘤的特征是上皮细胞增殖,类似于浅表高分化尿路上皮癌。一名29岁的患者因卵巢肿瘤接受了手术。大体检查显示,起源于左卵巢的肿瘤为囊性多房性,并呈现息肉样赘生物。最终的组织学检查显示,肿瘤为乳头状增殖,由移行细胞衬覆,无基质浸润。一些腔隙由黏液细胞衬覆。诊断为增殖性勃勒纳瘤。将讨论这种罕见实体的临床和病理特征。