Hummadi Abdul-Rahman A, Yahya Ayel O, Al-Qahtani Awad M
Department of Endocrinology & Internal Medicine, King Fahad Central Hospital, Jizan, Saudi Arabia.
Department of Family & Community Medicine, College of Medicine, Najran University, Najran, Saudi Arabia.
Sultan Qaboos Univ Med J. 2017 May;17(2):e218-e220. doi: 10.18295/squmj.2016.17.02.014. Epub 2017 Jun 20.
Deficiency of the 5-α-reductase enzyme has been found to affect male sexual development. We report an 18-year-old patient who was referred to an endocrinology clinic in Jizan, Saudi Arabia, in April 2014 with primary amenorrhoea, virilisation and a lack of secondary sex characteristics. As female external genitalia were present at birth, she had been raised as a female. Magnetic resonance imaging revealed no uterine or ovarian tissue in the pelvis and the presence of a scrotal sac. She was diagnosed with 5-α-reductase type 2 deficiency, a 46,XY disorder of sexual development. Typically, affected males have pseudovaginal perineoscrotal hypospadias and ambiguous genitalia at birth. Individuals who have been raised as female manifest characteristics of virilisation at puberty, including deepening of the vocal tone, enlargement, scrotal hyperpigmentation and increased muscle mass.
已发现5-α还原酶缺乏会影响男性性发育。我们报告一名18岁患者,2014年4月因原发性闭经、男性化和缺乏第二性征被转诊至沙特阿拉伯吉赞的一家内分泌诊所。由于出生时存在女性外生殖器,她一直被当作女性抚养。磁共振成像显示盆腔内无子宫或卵巢组织,且存在阴囊囊。她被诊断为2型5-α还原酶缺乏,这是一种46,XY性发育障碍。典型情况下,受影响的男性出生时患有假阴道会阴阴囊型尿道下裂和生殖器模糊。被当作女性抚养的个体在青春期会出现男性化特征,包括嗓音变深、阴蒂增大、阴囊色素沉着和肌肉量增加。