TY - JOUR
T1 - Juvenile granulosa cell tumour
T2 - Anaplastic variant with omental deposits
AU - Rao, A. C.K.
AU - Kishore, Manjari
AU - Monappa, Vidya
PY - 2016/2/1
Y1 - 2016/2/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84957109547&partnerID=8YFLogxK
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U2 - 10.7860/JCDR/2016/15207.7168
DO - 10.7860/JCDR/2016/15207.7168
M3 - Article
AN - SCOPUS:84957109547
SN - 2249-782X
VL - 10
SP - ED01-ED03
JO - Journal of Clinical and Diagnostic Research
JF - Journal of Clinical and Diagnostic Research
IS - 2
ER -