婴儿期卵巢性索间质肿瘤伴同性性早熟 1 例报告及文献复习
A rare case of Ovarian Juvenile Granulosa Cell Tumor in an Infant with Isosexual Pseudo Puberty and a Revision of Literature.
机构信息
Quisisana Hospital, Ferrara.
Pediatric Endocrinology Department, Hamad Medical Corporation.
出版信息
Acta Biomed. 2021 Sep 2;92(4):e2021319. doi: 10.23750/abm.v92i4.11572.
Abstract
Juvenile ovarian granulosa cell tumors (JGCTs) are described infrequently in pediatrics, and their finding in infants is exceptional. We highlight the presenting symptoms, radiologic images, operative management, and histopathologic findings of a 9-month-old female with isosexual pseudopuberty. An updated revision of literature in infants below the age of 12 months is also reported.
摘要
婴儿型卵巢颗粒细胞瘤（JGCT）在儿科中罕见报道，其在婴儿中的发现更是罕见。我们重点介绍了一例 9 月龄女性出现两性假性性早熟的临床表现、影像学表现、手术治疗及组织病理学检查结果。同时还对 12 月龄以下婴儿的相关文献进行了更新综述。
Zotero 插件