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생식아세포종을 동반한 Swyer씨 증후군에서 복강경적 성선제거 1 예
A Case of Gonadoblastoma with 46 , XY Swyers Syndrome
김경아(KA Kim),김재홍(JH Kim),권미숙(MS Kwon),유현(H Yoo),서승식(SS Suh),김영숙(YS Kim)
UCI I410-ECN-0102-2009-510-005352533
This article is 4 pages or less.

저자들은 표현형이 외견상 정상 여성이고 내생식기로 자궁 난관이 있고 일측에는 색상생식선과 반대측에 생식아세포종을 동반한 고환 퇴행증후군 중 Swyer씨 증후군 1예를 경험하였기에 간단한 문헌 고찰과 함께 보고하는 바이다.

Phenotypic female with a 46,XY Karyotype have approximately a 25% chance of developing a malignancy in the dysgenetic gonad. Malignancies occur in relatively young individuals. For this reason, it has been recommanded that all patients with Y-chromosomal material and dysgenetic gonads undergo gonadectomy. We report a case of gonadoblastoma with 46,XY Swyers syndrome, which was managed by laparoscopic adnexectomy.

[자료제공 : 네이버학술정보]
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