مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Cites:

1

Information Journal Paper

Title

Sclerosing Stromal Tumor: A Rare Ovarian Neoplasm

Pages

  402-405

Abstract

 Ovarian sex cord-stromal tumors are relatively infrequent neoplasms that account for approximately 8% of all primary ovarian neoplasm. Sex cord-stromal tumors of the ovary include granulosa cell tumors, fibrothecomas, Sertoli-Leydigcell tumors, steroid cell tumors, and Sclerosing stromal tumors (SST). Sclerosing stromal tumors account for 2% to 6% of ovarian stromal tumors. Despite the rarity of this particular neoplasm, it is not always possible to predict the presence of this tumor preoperatively on the basis of clinical and sonographic findings. Histopathological and immunohistochemical (IHC) examinations confirm the diagnosis. Herein, the clinical findings and histopathological features of SST are described in a 24-year-old female.

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  • Cite

    APA: Copy

    Bairwa, Shilpa, Satarkar, Rahul Narayan, Kalhan, Shivani, GARG, SHILPA, Sangwaiya, Ashok, & SINGH, PAWAN. (2017). Sclerosing Stromal Tumor: A Rare Ovarian Neoplasm. IRANIAN JOURNAL OF PATHOLOGY (IJP), 12(4), 402-405. SID. https://sid.ir/paper/729078/en

    Vancouver: Copy

    Bairwa Shilpa, Satarkar Rahul Narayan, Kalhan Shivani, GARG SHILPA, Sangwaiya Ashok, SINGH PAWAN. Sclerosing Stromal Tumor: A Rare Ovarian Neoplasm. IRANIAN JOURNAL OF PATHOLOGY (IJP)[Internet]. 2017;12(4):402-405. Available from: https://sid.ir/paper/729078/en

    IEEE: Copy

    Shilpa Bairwa, Rahul Narayan Satarkar, Shivani Kalhan, SHILPA GARG, Ashok Sangwaiya, and PAWAN SINGH, “Sclerosing Stromal Tumor: A Rare Ovarian Neoplasm,” IRANIAN JOURNAL OF PATHOLOGY (IJP), vol. 12, no. 4, pp. 402–405, 2017, [Online]. Available: https://sid.ir/paper/729078/en

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