Abstract

We report here an extremely rare case of proliferative Brenner tumor with borderline mucinous cystadenocarcinoma of the ovary, metastasizing to the pleura in a 75-year-old woman. Massive pleural effusion were present due to metastasis and pseudo-Meigs’ syndrome. The cytological findings from pleural effusion, ascites and tumor imprint were similar, suggesting mucus-producing malignant tumors. After receiving a thoracic drainage for pleural effusion, the patient underwent an exploratory laparotomy to remove the left-ovarian tumor. Histopathological examination revealed proliferative Brenner ovarian tumor with borderline mucinous cystadenocarcinoma, and immunohistochemical examinations for the tumors, even mucus-rich tumor cells were positive for CK 7 and negative for CK 20, suggesting the tumor arising from transitional cells, not from mucus-producing ovarian surface epithelial tumor cells. She underwent four courses of chemotherapy with paclitaxel and carboplatin. The patient showed no signs of recurrence 16 months after the surgery.

Highlights

  • Brenner tumors (BTs) of the ovary are rare epithelial tumors that account for 1% - 2% of all ovarian neoplasms

  • We present here an extremely rare case of proliferative BT with borderline mucinous cystadenocarcinoma of the ovary in a 75-year-old woman, in which immunohistochemistry of CK 7 and CK 20 was useful for the diagnosis

  • Ovarian BTs are rare adenofibromas that account for 1% - 2% of all ovarian neoplasms

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Summary

Introduction

Brenner tumors (BTs) of the ovary are rare epithelial tumors that account for 1% - 2% of all ovarian neoplasms. Proliferative BT of the ovary was first described in 1971 by Roth and Sternberg [1], and was confirmed by Miles and Norris [2]. The terms of borderline malignancy and proliferating in reference to BTs were equated in the WHO publication [3] It is a separate category of BT, being intermediate in its histologic appearance and biological aggressiveness compared with benign and malignant types of BTs [2][4][5]. We present here an extremely rare case of proliferative BT with borderline mucinous cystadenocarcinoma of the ovary in a 75-year-old woman, in which immunohistochemistry of CK 7 and CK 20 was useful for the diagnosis

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