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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Elsevier
2022
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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) |
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Juvenile granulosa cell tumor Alpha-inhibin Immunohistochemistry Ovarian sex cord-stromal tumors Pediatrics RJ1-570 Surgery RD1-811 |
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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 |
_version_ |
1718445288276885504 |