Torsion of juvenile granulosa cell ovarian tumor

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 juveni...

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Autores principales: Şenay Kurtuluş, Bülent Demir, Nilüfer Aylanç
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Lenguaje:EN
Publicado: Elsevier 2022
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Acceso en línea:https://doaj.org/article/961a9a606ca74fb7b0e5e948de07f30e
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spelling oai:doaj.org-article:961a9a606ca74fb7b0e5e948de07f30e2021-11-04T04:30:43ZTorsion of juvenile granulosa cell ovarian tumor2213-576610.1016/j.epsc.2021.102093https://doaj.org/article/961a9a606ca74fb7b0e5e948de07f30e2022-01-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2213576621003146https://doaj.org/toc/2213-5766Juvenile 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.Şenay KurtuluşBülent DemirNilüfer AylançElsevierarticleJuvenile granulosa cell tumorAlpha-inhibinImmunohistochemistryOvarian sex cord-stromal tumorsPediatricsRJ1-570SurgeryRD1-811ENJournal of Pediatric Surgery Case Reports, Vol 76, Iss , Pp 102093- (2022)
institution DOAJ
collection DOAJ
language EN
topic Juvenile granulosa cell tumor
Alpha-inhibin
Immunohistochemistry
Ovarian sex cord-stromal tumors
Pediatrics
RJ1-570
Surgery
RD1-811
spellingShingle Juvenile granulosa cell tumor
Alpha-inhibin
Immunohistochemistry
Ovarian sex cord-stromal tumors
Pediatrics
RJ1-570
Surgery
RD1-811
Şenay Kurtuluş
Bülent Demir
Nilüfer Aylanç
Torsion of juvenile granulosa cell ovarian tumor
description 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.
format article
author Şenay Kurtuluş
Bülent Demir
Nilüfer Aylanç
author_facet Şenay Kurtuluş
Bülent Demir
Nilüfer Aylanç
author_sort Şenay Kurtuluş
title Torsion of juvenile granulosa cell ovarian tumor
title_short Torsion of juvenile granulosa cell ovarian tumor
title_full Torsion of juvenile granulosa cell ovarian tumor
title_fullStr Torsion of juvenile granulosa cell ovarian tumor
title_full_unstemmed Torsion of juvenile granulosa cell ovarian tumor
title_sort torsion of juvenile granulosa cell ovarian tumor
publisher Elsevier
publishDate 2022
url https://doaj.org/article/961a9a606ca74fb7b0e5e948de07f30e
work_keys_str_mv AT senaykurtulus torsionofjuvenilegranulosacellovariantumor
AT bulentdemir torsionofjuvenilegranulosacellovariantumor
AT niluferaylanc torsionofjuvenilegranulosacellovariantumor
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