Borderline Brenner Tumor of the Ovary in a Postmenopausal Woman: A Rare Case with Concomitant Endometrial Hyperplasia and Endocervical Polyp

Naina Kumar, I. Pradeep, Annapurna Srirambhatla, K. Poojitha, M. Mangla
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Abstract

Bordeline Brenner tumors of the ovary are rare tumors accounting for 2% of all ovarian tumors and are characterized by the presence of papillary structures covered with transitional epithelium without or minimal stromal invasion. In the present case report a 60-year-old postmenopausal woman presented with complaints of lower abdominal pain and a right ovarian mass of 4x5cm, which was diagnosed on histopathological examination as borderline Brenner tumor of the ovary. There were coexisting nonatypical endometrial hyperplasia and endocervical polyps of 1.2x0.9x0.6cm, indicating endometrial hyperstimulation as a result of estrogen secreted by the tumor. The patient was managed successfully with staging laparotomy and was diagnosed with stage I borderline Brenner tumor with non-atypical endometrial hyperplasia and benign endocervical polyp. Borderline Brenner tumors are rare tumors of ovaries with uncertain malignant potential. They have no precise predictive markers but are known to produce estrogen. Surgery remains the mainstay of treatment for these tumors.
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一名绝经后妇女的卵巢边界布伦纳瘤:伴有子宫内膜增生和宫颈内膜息肉的罕见病例
在本病例报告中,一名 60 岁的绝经后妇女主诉下腹痛,右侧卵巢肿块 4x5 厘米,经组织病理学检查确诊为卵巢边界布伦纳肿瘤。患者同时伴有非典型子宫内膜增生和 1.2x0.9x0.6cm 的宫颈内膜息肉,表明肿瘤分泌的雌激素导致子宫内膜过度刺激。患者通过分期开腹手术成功接受了治疗,被诊断为边缘布伦纳肿瘤 I 期,伴有非典型子宫内膜增生和良性宫颈内膜息肉。边缘布伦纳肿瘤是一种罕见的卵巢肿瘤,恶性潜能不确定。手术仍是治疗这些肿瘤的主要方法。
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