Rajfer J, Mendelsohn G, Arnheim J, Jeffs R D, Walsh P C
J Urol. 1978 Apr;119(4):525-7. doi: 10.1016/s0022-5347(17)57536-9.
Dysgenetic male pseudohermaphroditism is a disorder of sexual differentiation in which patients present with bilateral dysgenetic testes, persistent müllerian structures, cryptorchidism and inadequate virilization. There were 10 patients with this syndrome seen at our hospital between 1956 and 1976. In this series, there was a 30 per cent incidence of testicular tumors. Because patients with dysgenetic male pseudohermaphroditism have a high incidence of testicular tumors this disorder, which is actually a variant of mixed gonadal dysgenesis, must be distinguished from the other forms of male pseudohermaphroditism.
发育不全性男性假两性畸形是一种性分化障碍,患者表现为双侧发育不全的睾丸、残留的苗勒管结构、隐睾症和男性化不足。1956年至1976年间,我院共收治了10例患有该综合征的患者。在这个系列中,睾丸肿瘤的发生率为30%。由于发育不全性男性假两性畸形患者睾丸肿瘤的发生率很高,这种实际上是混合性性腺发育不全变异型的疾病,必须与其他形式的男性假两性畸形相鉴别。