Juvenile granulosa cell ovarian tumor- a rare presentation

Authors

  • Eti Saha Asst. Prof., Khulna Medical College Khulna
  • Sunil Kumar Biswas Junior Consultant (Anes), General Hospital, Khulna
  • Dipanwita Saha OSD, BSMMU, Dhaka

DOI:

https://doi.org/10.3329/mediscope.v1i1.21636

Keywords:

Juvenile, granulosa cell, tumor

Abstract

Juvenile granulosa cell tumor is a rare gynecologic malignancy. A fourteen year old girl was brought to the emergency with acute abdominal pain with distension of abdomen and admitted in surgical unit, clinically suspected perforation of gut. Transabdominal ultrasonography revealed a right adenexal irregular mass with a moderate amount of ascitic fluid. On laparotomy, it was suspected malignant ovarian tumor stage Ic, and then ipsilateral salphingoophorectomy was done considering the age of the patient. It was juvenile Granulosa cell tumor which confirmed by histo-pathologically. The epidemiology, natural history, presentation, histological and imaging appearances, prognosis and treatment of this malignancy were reviewed.

DOI: http://dx.doi.org/10.3329/mediscope.v1i1.21636

Mediscope Vol. 1, No. 1: 2014, Pages 36-39

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Published

2015-01-15

How to Cite

Saha, E., Biswas, S. K., & Saha, D. (2015). Juvenile granulosa cell ovarian tumor- a rare presentation. Mediscope, 1(1), 36–39. https://doi.org/10.3329/mediscope.v1i1.21636

Issue

Vol. 1 No. 1 (2014)

Section

Case Reports

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