Huben R P, Devine P C, Harkins G A, Stecker J F
J Urol. 1981 Dec;126(6):849-51. doi: 10.1016/s0022-5347(17)54780-1.
Idiopathic female intersex can present with a varying phenotypic expression but generally includes clitoromegaly in association with either urogenital and/or cloacal anomalies. Additionally, absence of corporeal bodies may exist, resulting in either a markedly enlarged empty phallus or a megalourethra if developmental anomalies of the urogenital sinus occur in association with corporeal agenesis. Herein we report 2 cases to illustrate the spectrum of this disorder.
特发性女性两性畸形可表现出不同的表型，但一般包括阴蒂肥大伴泌尿生殖系统和/或泄殖腔异常。此外，可能不存在实体结构，如果泌尿生殖窦发育异常与实体结构发育不全同时出现，可导致阴茎显著增大但内部空虚或出现巨尿道。在此，我们报告2例病例以说明这种疾病的范围。
