Sclerosing Stromal Tumor of Ovary: A Case Report

Authors

  • R. Rana Lecturer, Department of Pathology, Birat Medical College & Teaching Hospital
  • S.U. Kafle Associate Professor, Department of Pathology, Birat Medical College & Teaching Hospital
  • K.K. Jha Lecturer, Department of Pathology, Birat Medical College & Teaching Hospital
  • M. Singh Lecturer, Department of Pathology, Birat Medical College & Teaching Hospital
  • P. Gautam Lecturer, Department of Pathology, Birat Medical College & Teaching Hospital

DOI:

https://doi.org/10.3126/bjhs.v1i1.17107

Keywords:

Pelvic mass, pseudolobulation, sclerosing stromal tumor

Abstract

A case of 32 year old female of pelvic pain for one month and with past history of hysterectomy performed two year back. Clinical examination revealed palpable abdominal pelvic mass. Ultrasonography showed right pelvic mass arising from right adnexa measuring 15cm x 15 cm, predominantly solid with some cystic areas. The patient was suspected of having a malignant ovarian tumor and hence operated. A histopathological diagnosis revealed sclerosing stromal tumor of ovary. Sex cord-stromal tumors account for approximately 8% of all ovarian tumor and prevalence of sclerosing stromal tumor of ovary is 1.5% to 6% .This rare neoplasm is not always possible to predict pre-operatively on the basis of clinical and radiological findings. Histologically, it is characterized by several unique features including pseudolobulation, sclerosis, and prominent vascularity. Sclerosing stromal tumor is rare but possibility of this tumor should be considered in young patients with ovarian mass having the characteristic histopathological morphology.

Birat Journal of Health Sciences 2016 1(1): 83-86

Downloads

Download data is not yet available.
Abstract
756
PDF
642

Downloads

Published

2017-03-31

How to Cite

Rana, R., Kafle, S., Jha, K., Singh, M., & Gautam, P. (2017). Sclerosing Stromal Tumor of Ovary: A Case Report. Birat Journal of Health Sciences, 1(1), 83–86. https://doi.org/10.3126/bjhs.v1i1.17107

Issue

Section

Case Reports