Malignant Brenner Tumour of the Ovary: A Rare Entity

Authors

  • Keshav Pagrut Department of Pathology, SVNGMC Yavatmal, Maharshtra
  • Virendra Khadse Department of Pathology, SVNGMC Yavatmal, Maharshtra
  • Sanjay Khandekar Department of Pathology, SVNGMC Yavatmal, Maharshtra
  • Jaywant Mahadani Department of Pathology, SVNGMC Yavatmal, Maharshtra

DOI:

https://doi.org/10.7439/ijbar.v7i9.3623

Abstract

Malignant Brenner tumors (MBTs) of the ovary are very rare, and their definition, biology and treatment modality have not been established. Most Brenner tumors are benign, with only 1% being malignant. In this study we present a case of 30 years old women with a rare malignant Brenner tumour. She presented at a peripheral referral hospital with a complaint of abdominal pain and mass. Ultrasonography revealed left sided ovarian tumours. She is referred for evaluation of a complex pelvic mass and elevated serum CA-125 level. She underwent left salpingo-oophorectomy and the specimen was sent for histopathological study. Histopathology revealed malignant Brenner tumour. Immunohistochemistry tumour cells are positive for pancytokeratin and negative for CK7/CK8/WT1/Pax8/CA125/calretinin/inhibin.

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References

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Published

2016-09-30

Issue

Section

Case Report

How to Cite

1.
Malignant Brenner Tumour of the Ovary: A Rare Entity. Int J of Biomed & Adv Res [Internet]. 2016 Sep. 30 [cited 2024 Oct. 18];7(9):479-81. Available from: https://ssjournals.co.in/index.php/ijbar/article/view/3623