Atıf İçin Kopyala
KURTULUŞ Ş., DEMİR B., AYLANÇ N.
JOURNAL OF PEDIATRIC SURGERY CASE REPORTS, cilt.76, 2022 (ESCI)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
76
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Basım Tarihi:
2022
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Doi Numarası:
10.1016/j.epsc.2021.102093
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Dergi Adı:
JOURNAL OF PEDIATRIC SURGERY CASE REPORTS
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Derginin Tarandığı İndeksler:
Emerging Sources Citation Index (ESCI), Scopus, EMBASE, Directory of Open Access Journals
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Anahtar Kelimeler:
Juvenile granulosa cell tumor, Alpha-inhibin, Immunohistochemistry, Ovarian sex cord-stromal tumors, CHILDREN, MANAGEMENT
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Çanakkale Onsekiz Mart Üniversitesi Adresli:
Evet
Özet
Juvenile granulosa cell tumor (JGCT), which is one of the sex cord-stromal tumors of the ovary, is a rare malignancy of childhood. Juvenile type is a rare form that accounts for 5% of granulosa cell tumors. Isosexual precocious puberty is the most common presentation in prepubertal girls with juvenile granulosa cell tumors. Less frequently, they present with the complaint of a mass in the abdomen.