国际妇产科学杂志 ›› 2025, Vol. 52 ›› Issue (3): 354-357.doi: 10.12280/gjfckx.20241005

• 妇科肿瘤研究: 病例报告 • 上一篇    下一篇

卵巢非特异性类固醇细胞瘤一例

黄银波, 王颖, 李翠红, 车力凡()   

  1. 261000 潍坊,山东第二医科大学临床医学院(黄银波);潍坊市益都中心医院(王颖,李翠红,车力凡)
  • 收稿日期:2024-11-08 出版日期:2025-06-15 发布日期:2025-06-19
  • 通讯作者: 车力凡 E-mail:qzchelifan@126.com

Ovarian Steroid Cell Tumor, Not Otherwise Specified: A Case Report

HUANG Yin-bo, WANG Ying, LI Cui-hong, CHE Li-fan()   

  1. School of Clinical Medicine, Shandong Second Medical University, Weifang 261000, Shandong Province, China (HUANG Yin-bo);Yidu Central Hospital of Weifang, Weifang 262500, Shandong Province, China (WANG Ying, LI Cui-hong, CHE Li-fan)
  • Received:2024-11-08 Published:2025-06-15 Online:2025-06-19
  • Contact: CHE Li-fan E-mail:qzchelifan@126.com

摘要:

卵巢非特异性类固醇细胞瘤(steroid cell tumor,not otherwise specified,SCT-NOS)是一种临床较为罕见的卵巢肿瘤,且具有一定的恶性潜能。患者通常表现出男性化的体征,并且伴有雄激素水平的异常升高。卵巢SCT-NOS的影像学检查无特异性,因此术前诊断比较困难。报告1例卵巢SCT-NOS的病例资料,患者因发现腹部包块7 d,下腹痛1 d收入院,妇科彩色超声显示盆腔异常囊性肿物,不除外扭转,初步诊断为腹腔囊肿,行腔镜下左侧卵巢肿瘤切除术,术后病理诊断为左侧卵巢SCT-NOS。患者出院后失访。

关键词: 卵巢肿瘤, 性索-性腺间质瘤, 免疫组织化学, 病例报告, 非特异性类固醇细胞瘤

Abstract:

Ovarian steroid cell tumor, not otherwise specified (SCT-NOS) is a relatively rare ovarian tumor in clinical practice and has certain malignant potential. Patients usually present with virilization signs and are accompanied by abnormally elevated androgen levels. The imaging examination of ovarian SCT-NOS is non-specific, so the preoperative diagnosis is quite difficult. This paper reports a case of ovarian SCT-NOS. The patient was admitted to the hospital due to a 7-day discovery of an abdominal mass and 1-day lower abdominal pain. Gynecological color ultrasound showed an abnormal cystic pelvic mass in the pelvis, torsion was not excluded, and the initially diagnosis was an abdominal cyst. Laparoscopic resection of the left ovarian tumor was performed, and the postoperative pathological diagnosis was left ovarian SCT-NOS. The patient was lost to follow-up after discharge.

Key words: Ovarian neoplasms, Sex cord-gonadal stromal tumors, Immunohistochemistry, Case reports, Steroid cell tumor, not otherwise specified