Bosković Tamara, Dolai Matilda, Ilić Jelena, Zivojinov Mirjana, Kaćanski Mihaela Mocko, Milić Miljan
Klinicki centar Vojvodine, Centar za patologiju i histologiju.
Med Pregl. 2012 Nov-Dec;65(11-12):527-9. doi: 10.2298/mpns1212527b.
Cystadenofibromas are tumors of the ovary which originate from the surface coelomic epithelium. Benign mucinous cystadenofibroma is a very rare form of these tumors, which consists of dominant stromal component of the connective tissue and one or more cysts.
The case of a 62-year-old female with tumor of right ovary is reported in this paper. Histologically, tumor of the ovary had multilocular cystic formation, lined by a single-layer of mucoproductive cylindrical epithelium - endocervical type. In one area of tumor, the stromal component was abundant and made from partially hyalinised dense connective tissue. Mucinous cystadenofibroma was diagnosed on the basis of histological examination. Since the mucinous type of cystadenofibroma or adenofibroma is rare, this case has been chosen to be presented.
Mucinous cystadenofibromas are differentially-diagnostically very similar to different malignant tumors and it is extremely important to make correct diagnosis of these neoplasms.
囊腺纤维瘤是起源于体腔上皮的卵巢肿瘤。良性黏液性囊腺纤维瘤是这些肿瘤中非常罕见的一种形式，它由结缔组织的主要间质成分和一个或多个囊肿组成。
本文报告了一例62岁患有右卵巢肿瘤的女性病例。组织学上，卵巢肿瘤呈多房囊性结构，内衬单层黏液分泌柱状上皮——宫颈内膜型。在肿瘤的一个区域，间质成分丰富，由部分玻璃样变的致密结缔组织构成。根据组织学检查诊断为黏液性囊腺纤维瘤。由于黏液型囊腺纤维瘤或腺纤维瘤较为罕见，故选择此病例进行展示。
黏液性囊腺纤维瘤在鉴别诊断上与不同的恶性肿瘤非常相似，对这些肿瘤做出正确诊断极其重要。
