国际生殖健康/计划生育杂志 ›› 2025, Vol. 44 ›› Issue (5): 388-392.doi: 10.12280/gjszjk.20250129

• 病例报告 • 上一篇    下一篇

卵巢非特异性类固醇细胞瘤伴大量腹水一例

刘琴, 郑嵘()   

  1. 430065 武汉科技大学医学院(刘琴); 湖北省妇幼保健院妇科(郑嵘)
  • 收稿日期:2025-03-20 出版日期:2025-09-15 发布日期:2025-09-12
  • 通讯作者: 郑嵘 E-mail:zhengrong@163.com

A Case Report of Ovarian Steroid Cell Tumor-Not Otherwise Specified with Ascites

LIU Qin, ZHENG Rong()   

  1. School of Medicine, Wuhan University of Science and Technology, Wuhan 430065, China (LIU Qin); Department of Gynecology, Maternal and Child Health Hospital of Hubei Province, Wuhan 430070, China (ZHENG Rong)
  • Received:2025-03-20 Published:2025-09-15 Online:2025-09-12
  • Contact: ZHENG Rong E-mail:zhengrong@163.com

摘要:

卵巢非特异性类固醇细胞瘤(steroid cell tumor-not otherwise specified,SCT-NOS)是一种罕见的卵巢单纯性间质肿瘤,具有恶性潜能,发病率极低,临床罕见,易误诊漏诊。报告1例育龄期卵巢SCT-NOS伴大量腹水的病例,患者因经间期阴道出血半年,彩色超声提示右侧附件区肿物伴盆腹腔大量积液入院。入院后完善盆腔磁共振成像,经多学科会诊,行经腹右侧输卵管卵巢切除术+左侧卵巢活组织检查。术后病理确诊右侧卵巢SCT-NOS,术后随访1年未见腹水及肿瘤复发。结合此病例回顾相关文献,总结卵巢SCT-NOS的流行病学、临床特点、诊断及鉴别诊断、治疗及预后,旨在为该病的临床诊疗提供参考。

关键词: 卵巢肿瘤, 腹水, 诊断, 治疗, 卵巢非特异性类固醇细胞瘤

Abstract:

Ovarian steroid cell tumor-not otherwise specified (SCT-NOS) is an exceedingly rare subtype of pure ovarian stromal tumor with malignant potential. Due to its low incidence and nonspecific clinical manifestations, it is frequently misdiagnosed or overlooked, with only sporadic cases reported in the literature. We report a case of ovarian SCT-NOS in a reproductive-aged woman presenting with massive ascites. The patient was admitted with a six-month history of intermenstrual vaginal bleeding. Color Doppler ultrasound revealed a right adnexal mass accompanied by significant pelvic and abdominal effusion. Pelvic magnetic resonance imaging was performed. After that, the multi-disciplinary team recommended exploratory laparotomy. The patient underwent a right salpingo-oophorectomy with left ovarian biopsy. Histopathological examination confirmed the diagnosis of right ovarian SCT-NOS. The postoperative follow-up at one year showed no evidence of ascites recurrence or tumor progression. Based on this case and a comprehensive literature review, we discuss the epidemiology, clinical characteristics, diagnostic challenges (including differential diagnoses), management strategies, and prognostic factors of SCT-NOS, with the aims to enhance clinical awareness and provide references for the diagnosis and treatment of this rare entity.

Key words: Ovarian neoplasms, Ascites, Diagnosis, Therapy, Ovarian steroid cell tumor-not otherwise specified