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Juvenile Granulosa Cell Tumour: Anaplastic Variant with Omental Deposits
Author(s) -
Anjali Rao,
Manjari Kishore,
Vidya Monappa
Publication year - 2016
Publication title -
journal of clinical and diagnostic research
Language(s) - Uncategorized
Resource type - Journals
eISSN - 2249-782X
pISSN - 0973-709X
DOI - 10.7860/jcdr/2016/15207.7168
Subject(s) - anaplasia , granulosa cell , ovary , juvenile , biology , cell of origin , pathology , cell , endocrinology , medicine , genetics
Juvenile Granulosa Cell Tumour (JGCT) of ovary represents a small fraction of all primary ovarian malignancies. It is a subtype of granulosa cell tumour that is almost always found during the first three decades of life. Histologically, it differs from the typical adult type of granulosa cell tumour. It accounts for 5-15% of all granulosa cell tumours, majority being unilateral. Herein, we describe an unusual histopathological variant of JGCT with numerous large cystic spaces, anaplasia and focal syncytiotrophoblast like giant cells.

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