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Cystic Juvenile Granulosa Cell Tumor of the Ovary
Author(s) -
Spaun E.,
Glavind K.
Publication year - 1988
Publication title -
acta obstetricia et gynecologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 102
eISSN - 1600-0412
pISSN - 0001-6349
DOI - 10.3109/00016348809004195
Subject(s) - granulosa cell , ovary , medicine , stromal cell , pathology , juvenile , biology , genetics
. Sex cord‐stromal tumors comprise approximately 5% of ovarian neoplasms and among these the granulosa cell tumor is the one most commonly seen (1). Two histopathologically well defined patterns of granulosa cell tumor are known: the common adult granulosa cell tumor (AGCT), and the less frequent juvenile granulosa cell tumor (JGCT) (1,2,3,4). In addition to morphological variation, the two tumor types differ in prognosis and clinical course (4,5,6,7,8).

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