Yadav Alka, Pujani Mukta, Singh Kanika, Chauhan Varsha, Singh Aparna, Sharma Jagadish Chandra
Department of Pathology, ESIC Medical College and Hospital, Faridabad, Haryana, India.
Department of Obstetrics and Gynaecology, ESIC Medical College and Hospital, Faridabad, Haryana, India.
J Midlife Health. 2023 Jan-Mar;14(1):56-59. doi: 10.4103/jmh.jmh_26_22. Epub 2023 Jul 7.
Ovarian tumors are a common form of neoplasia in women and it accounts for about 30% of female genital cancers. A coexistence of ovarian tumors with the same histogenetic origin such as germ cell or epithelial or sex cord stromal, but different histologic subtype is relatively common, whereas a synchronous occurrence of tumors with different histogenetic origin is rare. We report a case of 58-year-old woman with the synchronous presentation of adult granulosa cell tumor with fibroma (ovarian tumors with the same origin (sex cord stromal) but different histologic type) in one ovary and Brenner tumor (epithelial origin) in other ovary. Our patient presented with postmenopausal bleeding and was diagnosed with this rare combination of ovarian tumors on histopathology supplemented with immunohistochemistry. On extensive literary search, there is only a single report of mixed ovarian tumor composed of Brenner tumor and adult-type granulosa cell tumor. Our case is different from the above-mentioned report as although, in our patient both tumors coexisted, but in contralateral ovaries.
卵巢肿瘤是女性肿瘤的常见形式,约占女性生殖系统癌症的30%。起源于同一组织发生学类型(如生殖细胞、上皮或性索间质)但组织学亚型不同的卵巢肿瘤共存较为常见,而起源于不同组织发生学类型的肿瘤同时出现则较为罕见。我们报告一例58岁女性,其一侧卵巢同时出现成人颗粒细胞瘤和纤维瘤(起源相同(性索间质)但组织学类型不同的卵巢肿瘤),另一侧卵巢出现勃勒纳瘤(上皮起源)。我们的患者表现为绝经后出血,经组织病理学检查并辅以免疫组化诊断为这种罕见的卵巢肿瘤组合。经广泛文献检索,仅有一篇关于由勃勒纳瘤和成人型颗粒细胞瘤组成的混合性卵巢肿瘤的报道。我们的病例与上述报道不同,尽管在我们的患者中两种肿瘤共存,但位于对侧卵巢。