首页 | 本学科首页   官方微博 | 高级检索  
检索        


Dysgerminoma in a 10-Year Old with 45X/46XY Turner Syndrome Mosaicism
Authors:Tazim Dowlut-McElroy  Denise A Vilchez  Eugenio M Taboada  Julie L Strickland
Institution:1. Department of Surgery, Children''s Mercy Hospitals, Kansas City, MO;2. OB/GYN Specialists of the Palm Beaches, Wellington, FL;3. Department of Pathology and Laboratory Medicine, Children''s Mercy Hospitals, Kansas City, MO
Abstract:BackgroundTurner syndrome is a genetic disorder resulting from the absence of or structural abnormality of one X chromosome. The presence of Y chromosome material in girls with Turner syndrome confers an increased risk of benign and malignant germ cell tumor and prophylactic bilateral gonadectomy is recommended.CaseA 10-year-old Turner mosaic syndrome (45X/46XY) patient underwent prophylactic gonadectomy after unremarkable preoperative pelvic imaging. Histopathology showed a streak right gonad, and left gonad with gonadoblastoma with limited degree of infiltrating germinoma.Summaryand ConclusionGonadoblastoma and dysgerminoma have been reported in girls with Turner mosaic who carry Y chromosome material. Prophylactic gonadectomy should be considered in these girls without delay.
Keywords:Turner syndrome  Mosaic  Gonadoblastoma  Dysgerminoma
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号