A Case of Coincidental Gonadoblastoma and Dysgerminoma in 45X/47XYY Mosaic Turner Variant.
- Author:
Seung Chul KIM
1
;
Seung Sup PARK
;
Ki Hyung KIM
;
Do Yoon PARK
;
Man Soo YOON
Author Information
1. Department of Obstetrics and Gynecology, Pusan National University, Pusan, Korea. msyoon@pusan.ac.kr
- Publication Type:Case Report
- Keywords:
45X/47XYY mosaicism;
Gonadoblastoma;
Dysgerminoma
- MeSH:
Adolescent;
Chromosome Disorders;
Dysgerminoma*;
Female;
Gonadoblastoma*;
Gonads;
Humans;
Mosaicism
- From:Korean Journal of Obstetrics and Gynecology
2005;48(7):1805-1810
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
45X/47XYY mosaicism is a very rare sex chromosomal disorder with limited clinical information. We experienced an unusual mosaic syndrome in a 16-year old woman with a phenotypic female, short stature, and immature secondary sexual characteristics. We performed both gonadectomy and found a gonadoblastoma in one gonad and dysgerminoma in another gonad.
