Objective Juvenile type granulosa cell tumor (JGCTs) are extremely rare, mainly diagnosed
in young women and pre-pubertal girls at stage I disease. Literature is scanty and guidelines …

Ovarian neoplasms are relatively rare in childhood and adolescence; only 5% to 8% of the
cases are of sex cord stromal origin. Granulosa cell tumors are a group of estrogen …

Hormone‑producing malignancies are rare in children or adolescent patients: Only 0.1% of
all ovarian tumors and 4-5% of granulosa cell tumors occur in the sexually non‑active ages …

[Table/Fig-3]. Final histopathological diagnosis given as juvenile granulosa cell tumour of
left ovary. Most of the juvenile GCTs presented with clinical evidence of precocious pseudo …

Objective: Rare disease Background: Juvenile-type granulosa cell tumors (JGCTs) are a
rare subtype of sex cord stromal tumor with a characteristic histology that is commonly found …

Introduction Although female victims of sexual child abuse present with symptoms such as
local pain and vaginal bleeding, however, before any definitive diagnosis a comprehensive …

We report a rare case of virilizing cystic juvenile granulosa cell tumour of the ovary
diagnosed by histopathological examination in a 17-year-old female presented with mass …

Differentiation of granulosa cell tumor and ovarian cancer doesn't seem to cause much
trouble in everyday clinical work. Despite quite easy distinction, within the researches …

Precocious puberty in girls is generally defined as appearance of secondary sexual
characteristics before eight years of age. Precocious puberty is divided into central …

Ovarialtumoren gehören zu den fünf häufigsten Tumoren der Frau in der westlichen Welt [1].
Mit 3, 2% aller bösartigen Neubildungen der Frauen und 5, 3% aller Krebssterbefälle ist der …