Gupta M M, Grover D N
J Urol. 1978 Jan;119(1):143-4. doi: 10.1016/s0022-5347(17)57413-3.
A case of XXY Klinefelter's syndrome associated with bilateral cryptochidism, -ultiple capillary hemangiomas and vesical telangiectasia is reported. Testicular biopsy revealed Leydig cell hyperplasia with hyalinization of the seminiferous tubular membrane. The patient presented with recurrent hematuria. Excretory urography, urethroscopy and renal angiography were normal. Cystoscopy revealed multiple telangiectasia, which was responsible for the hematuria. To our knowledge this is the first report of multiple capillary hemangiomas and vesical telangiectasia associated with calssical Klinefelter's syndrome.
报告了一例XXY克氏综合征合并双侧隐睾、多发性毛细血管瘤和膀胱毛细血管扩张症的病例。睾丸活检显示间质细胞增生伴生精小管膜玻璃样变。患者出现反复血尿。排泄性尿路造影、尿道镜检查和肾血管造影均正常。膀胱镜检查发现多处毛细血管扩张,这是血尿的原因。据我们所知,这是首例与典型克氏综合征相关的多发性毛细血管瘤和膀胱毛细血管扩张症的报告。