Cattolica E V, Solomon I L
J Urol. 1978 Jul;120(1):103-5. doi: 10.1016/s0022-5347(17)57061-5.
The mosaic karyotype XO/XY is expressed by a spectrum of genital phenotypes, ranging from normal male through ambiguous genitalia to normal female. The urologist may see some of these patients because of the following clinical presentations: 1) ambiguous genitalia with a chromatin-negative buccal smear, 2) hypospadias with cryptorchidism or 3) cryptorchidism with müllerian remnants, discovered unexpectedly during inguinal operations. Reliable karyotyping is mandatory for diagnosis of XO/XY patients. Management should include laparotomy with excision of any intra-abdominal gonads (testis and/or streak gonad) because these are prone to develop malignancies that may occur before puberty. Female sex assignment and a reconstructive operation are advised in cases with severely deficient virilization of the genitalia.
嵌合核型XO/XY表现为一系列生殖器表型,从正常男性到生殖器模糊再到正常女性。泌尿科医生可能会因为以下临床表现而诊治其中一些患者:1)生殖器模糊且口腔涂片染色质阴性;2)伴有隐睾的尿道下裂;或3)在腹股沟手术中意外发现的伴有苗勒管残余的隐睾。对于XO/XY患者的诊断,可靠的核型分析是必不可少的。治疗应包括剖腹手术,切除任何腹内性腺(睾丸和/或条索状性腺),因为这些性腺容易发生在青春期前可能出现的恶性肿瘤。对于生殖器严重男性化不足的病例,建议进行女性性别指定和重建手术。