...
首页> 外文期刊>Journal of Medical Case Reports >Precocious puberty secondary to a mixed germ cell-sex cord-stromal tumor associated with an ovarian yolk sac tumor: a case report
【24h】

Precocious puberty secondary to a mixed germ cell-sex cord-stromal tumor associated with an ovarian yolk sac tumor: a case report

机译:混合性生殖细胞-性索-间质混合性肿瘤继发于卵巢卵黄囊肿瘤的性早熟:一例

获取原文
           

摘要

Introduction Ovarian tumors are the least common cause of sexual precocity in girls. Mixed germ cell-sex cord-stromal tumors associated with a yolk sac tumor of the ovary are rare neoplasms, of which only a small number of well-documented cases have been described so far. Here, we report precocious puberty in a four-year-old Egyptian girl caused by a mixed germ cell-sex cord-stromal tumor associated with a yolk sac tumor of the ovary. Case presentation A four-year-old Egyptian girl was referred to our pediatric endocrinology unit for evaluation of bilateral breast budding, pubic hair and vaginal bleeding. On examination, we found that her breast enlargement and pubic hair were compatible with Tanner III. A thorough workup revealed a large mass in her right ovary. Magnetic resonance imaging ofher brain showed that her pituitary gland was normal. A hormonal assay revealed high levels of estradiol, 280 to 375pmol/L; progesterone, 5.3?nmol/L; testosterone 38.9?pg/mL; and androstenedione, 4.1?ng/mL. Her basal and stimulated levels of luteinizing hormone and follicle-stimulating hormone were low. Tumor markers levels were high, with a total inhibin of 1,069U/L and an alpha-fetoprotein of 987?μg/L. Her chromosomes were normal (46XX). Our patient underwent an explorative laparotomy and a solid tumor localized to her right ovary was identified. A right salpingo-oophorectomy was performed and the histopathological diagnosis was a mixed germ cell-sex cord-stromal tumorwith a yolk sac tumor of the ovary. Postoperatively, she was started on treatment with chemotherapy. Our patient is doing well without evidence of tumor recurrence or metastasis during eight months of postoperative follow-up. Conclusion Although a mixed germ cell-sex cord-stromal tumor associated with a yolk sac tumor of the ovary is a rare occurrence, it should be considered in the differential diagnosis for a prepubescent girl with an abdominal mass and precocious puberty.
机译:简介卵巢肿瘤是女孩发生性早熟的最不常见原因。与卵巢卵黄囊肿瘤相关的混合生殖细胞-性索-间质肿瘤是罕见的肿瘤,迄今为止,仅描述了少数充分记载的病例。在这里,我们报道了一个由混合生殖细胞-性索-间质瘤与卵巢卵黄囊瘤相关的四岁埃及女孩性早熟。病例介绍一名四岁的埃及女孩被转诊至我们的儿科内分泌科,以评估双侧乳房发芽,阴毛和阴道出血。经检查,我们发现她的乳房增大和阴毛与Tanner III兼容。彻底检查发现她的右卵巢有大量肿块。她的大脑的磁共振成像显示她的垂体正常。激素测定表明雌二醇水平较高,为280至375pmol / L。孕酮5.3?nmol / L;睾丸激素38.9?pg / mL;和雄烯二酮,4.1?ng / mL。黄体生成素和促卵泡激素的基础和刺激水平很低。肿瘤标志物水平高,总抑制素为1,069U / L,甲胎蛋白为987?μg/ L。她的染色体正常(46XX)。我们的患者进行了一次探索性剖腹手术,并发现了一个位于右卵巢的实体瘤。进行了右侧输卵管卵巢切除术,组织病理学诊断为混合生殖细胞-性索-间质瘤与卵巢卵黄囊瘤。术后,她开始接受化学疗法治疗。我们的患者在术后八个月的随访中表现良好,没有肿瘤复发或转移的迹象。结论尽管混合性生殖细胞-性索-间质性肿瘤伴有卵巢卵黄囊瘤的情况很少见,但在鉴别具有腹部肿块和性早熟的青春期女孩时应考虑使用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号