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永存苗勒氏管综合征(Persistent Mnllerrian Duct Syndrome)较为少见,Nilson氏在1939年首先报道此症,迄今国内外文献报告近100例。我们自1988年9月至1989年1月期间遇到2例,现报告如下: 例1 陈某某,10岁,因右侧睾丸缺如伴尿道开口异位,于1988年9月20日入本院外科诊治。患儿无外伤,手术史,家族成员中无类似病员。检查:第二性征未发育,阴茎比正常儿童小,龟头外露下垂,尿道开口异位在龟头系带上O.2cm处。右侧阴囊空虚,无压痛,未扪及睾丸。右侧腹股沟膨隆无
Persistent Mnllerrian Duct Syndrome is rare. Nilson’s first report of this disease in 1939, so far nearly 100 cases reported in domestic and foreign literature. We have encountered from September 1988 to January 1989 in 2 cases, the report is as follows: Example 1 Moumou Mou, 10 years old, because the right testicular absence with urethral opening ectopic, on September 20, 1988 into Hospital surgical treatment. Children without trauma, history of surgery, no similar members of family members. Check: The second sexual characteristics are not developed, the penis smaller than normal children, penis exposed sagging, urethral ectopic opening in the glans lace at O.2cm Department. Right scrotum empty, no tenderness, no palpable testicles. Right groin swelling no