Accessory ovarian steroid cell tumor producing testosterone and cortisol A case report

被引:9
作者
Zang, Li [1 ]
Ye, Mingxia [2 ]
Yang, Guoqing [1 ]
Li, Jinlong [3 ]
Liu, Mei [3 ]
Du, Jin [1 ]
Gu, Weijun [1 ]
Jin, Nan [1 ]
Yang, Lijuan [1 ]
Ba, Jianming [1 ]
Dou, Jingtao [1 ]
Fan, Wensheng [2 ]
Mu, Yiming [1 ]
Meng, Yuanguang [2 ]
Lyu, Zhaohui [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Endocrinol, 28 Fuxing Rd, Beijing 100853, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Dept Gynecol, 28 Fuxing Rd, Beijing 100853, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Dept Pathol, Beijing, Peoples R China
关键词
accessory ovary; Cushing syndrome; hyperandrogenemia; steroid cell tumor;
D O I
10.1097/MD.0000000000007998
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: An accessory ovary is a rare structure containing normal ovarian tissue, which has a direct or ligamentous connection with a normal and eutopic ovary. Patient concerns: In the study, we reported a 46-year-old woman presented with secondary amenorrhea and virilization symptoms for 1 year. Diagnoses: Endocrine evaluation revealed slightly elevated serum cortisol, extremely elevated 24-hour urinary-free cortisol and serum testosterone. Clinical assessment exhibited a large solid mass with heterogeneous enhancement in the left adnexauteri compounded with hypercortisolism and hyperandrogenemia. An accessory ovarian tumor attached to the infundibulum of the left fallopian tube was found, and a separate normal ovary was present on the same side. Interventions: The patient underwent a left adnexectomy. Outcomes: During surgery, a 12cm x 8cm, gray-red, and well-circumscribed solid mass was be identified. The tumor had ligamentous attachment with the infundibulum of left fallopian tube. The sectioned surface was gray-brown, lobulated and did not exhibit either significant necrosis or hemorrhage. Pathological findings demonstrated that tumor cells had small round nuclei, mild atypia, no mitosis were arranged in a diffuse pattern of columns or nests separated by a rich vascular network and no crystals of Reinke were found. It was diagnosis ovarian steroid cell tumor (NOS) without malignant behavior by immunohistochemical staining. The patient was finally diagnosed as accessory ovarian steroid. The patient was discharged from the hospital on the seventeenth day after surgery. During postoperative follow-up, the first postoperative menstrual flow recovered and blood pressure regained 1 month after surgery. Furthermore, her Cushing syndrome regressed and hirsutism disappeared completely 4 months after surgery cell tumor. Lessons: It is vitally important to establish a final diagnosis according to the clinical manifestations and laboratory values in addition to imaging studies and laparoscopic examination of a rare coexistence of hyperandrogenemia and Cushing syndrome based on the accessory ovarian pathology.
引用
收藏
页数:4
相关论文
共 35 条
  • [31] ACTH-producing small cell neuroendocrine carcinoma from the gallbladder: a case report and literature review
    Zhang, Xiaofang
    Huang, Dihua
    Pan, Xiaojie
    Si, Qiya
    You, Qiaoying
    FRONTIERS IN ENDOCRINOLOGY, 2023, 14
  • [32] Postmenopausal mild hirsutism and hyperandrogenemia due to granulosa cell tumor of the ovary: A case report
    Adefris M.
    Fekadu E.
    Journal of Medical Case Reports, 11 (1)
  • [33] Sex Cord-stromal Tumors With Steroid Cell Tumor and Fibroma Components: Report of 2 Cases, Including One of Extraovarian Origin
    Wong, Richard Wing-Cheuk
    McCluggage, W. Glenn
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 2019, 38 (02) : 151 - 156
  • [34] Leydig-Cell-Tumor of the Ovary that Responded to GnRH-Analogue Administration - Case Report and Review of the Literature
    Klotz, R. K.
    Mueller-Holzner, E.
    Fessler, S.
    Reimer, D. U.
    Zervomanolakis, I.
    Seeber, B.
    Mattle, V.
    Wildt, L.
    EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2010, 118 (05) : 291 - 297
  • [35] Cushing's syndrome secondary to ectopic ACTH secretion from carcinoid tumor within an ovarian mature teratoma: a case report and review of the literature
    Huang, Baoyou
    Wu, Xueqing
    Zhou, Qing
    Hu, Yan
    Zhao, Hongqin
    Zhu, Hua
    Zhang, Qian
    Zheng, Feiyun
    GYNECOLOGICAL ENDOCRINOLOGY, 2014, 30 (03) : 192 - 196