Torsion of juvenile granulosa cell ovarian tumor
Yükleniyor...
Tarih
2022
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Elsevier Inc.
Erişim Hakkı
info:eu-repo/semantics/openAccess
Attribution-NonCommercial-NoDerivs 3.0 United States
Attribution-NonCommercial-NoDerivs 3.0 United States
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. We present an 8-year-old girl with a juvenile granulosa cell tumor who presented with sudden onset of abdominal pain and enlargement of the abdomen. She underwent exploratory laparotomy with right salpingo-oophorectomy and a complete mass resection was performed. Pathologic staging of the mass, which was diagnosed as juvenile granulosa cell tumor of the ovary, was determined as pT1c3, and our patient received four cycles of chemotherapy.
Açıklama
Anahtar Kelimeler
Alpha-inhibin, Immunohistochemistry, Juvenile granulosa cell tumor, Ovarian sex cord-stromal tumors
Kaynak
Journal of Pediatric Surgery Case Reports
WoS Q Değeri
N/A
Scopus Q Değeri
Cilt
76
Sayı
Künye
Kurtuluş, Demir, B., & Aylanç, N. (2022). Torsion of juvenile granulosa cell ovarian tumor. Journal of Pediatric Surgery Case Reports, 76 doi:10.1016/j.epsc.2021.102093
