一名15岁具有46, XY单纯性腺发育不全的表型女性斯维尔综合征患者发生无性细胞瘤：病例报告。
Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report.
作者信息
Ashraf Ganjooei Tahereh, Pirastehfar Zanbagh, Mosallanejad Asieh, Raoufi Masoomeh, Afshar Moghaddam Noushin, Hashemieh Mozhgan
机构信息
Department of Obstetrics and Gynecology, School of Medicine, Preventative Gynecology Research Center, Imam Hossein Medical Center Shahid Beheshti University of Medical Sciences Tehran Iran.
Department of Obstetrics and Gynecology, School of Medicine, Imam Khomeini Hospital Mazandaran University of Medical Sciences Sari Iran.
出版信息
Clin Case Rep. 2022 Jul 14;10(7):e6083. doi: 10.1002/ccr3.6083. eCollection 2022 Jul.
Swyer syndrome is a 46, XY karyotype, with pure gonadal dysgenesis and primary amenorrhea. These females have primordial Mullerian structures and seek medical attention as they experience primary amenorrhea. Here, we report a 15-year-old girl, diagnosed as Swyer syndrome associated with left ovarian dysgerminoma.
斯维尔综合征是一种核型为46, XY的疾病，伴有单纯性腺发育不全和原发性闭经。这些女性具有原始的苗勒管结构，因原发性闭经而寻求医疗帮助。在此，我们报告一名15岁女孩，被诊断为与左侧卵巢无性细胞瘤相关的斯维尔综合征。
Zotero 插件