Ovarian Juvenile Granulosa Cell Tumor in A 2.5 Years-Old Girl: The Importance of Early Diagnosis
Iranian Journal of Pediatric Surgery,
Vol. 9 No. 1 (2023),
11 Ordibehesht 2023
,
Page 120-125
https://doi.org/10.22037/irjps.v9i1.35714
Abstract
Juvenile granulosa tumor is a rare tumor in infant. The diagnosis should be discussed in any ovarian tumor of children, especially in front of the early signs of puberty. The prognosis of granulosa cell tumors remains good. The main prognostic factor is the stage of local extension. Early diagnosis at early signs of puberty is an important prognostic factor. We describe the case of a girl aged 2 years and 5 months who presented signs of early puberty. The diagnosis was a secreting ovarian tumor but was very large at that time. We focus by this observation on the value of early diagnosis of this tumor type which remains a key prognostic factor.
- ovary ; juvenile granulosa tumor ; early puberty ; infant
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References
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Nishida M, Jimi S, Haji M, et al; Juvenile granulosa cell tumor in association with a high serum inhibin level. Gynecologic oncology. 1991 Jan 1;40(1):90-4.
Bouffet E, Basset T, Chetail N, et al; Juvenile granulosa cell tumor of the ovary in infants: a clinicopathologic study of three cases and review of the literature. Journal of pediatric surgery. 1997 May 1;32(5):762-5.
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