Abstract
Juvenile granulosa cell tumor (JGCT) is a rare subtype of ovarian sex cord-stromal tumors. Its reported incidence is between 0.58–1.6/100 000/year, with 90% of the JGCT occurring in young females less than 30 years of age, and only up to 5% diagnosed in prepubertal age. JGCT is included in a European network for very rare tumors in childhood (European Cooperative Study Group for Pediatric Rare Tumors: EXPeRT) which has been founded in 2008 to improve knowledge, diagnosis and treatment of rare pediatric cancers (Bisogno G et al., Klin Padiatr 2012; 224: 416–420).
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