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作 者:王养民[1] 鲁守琳[1] 常德辉[1] 张晓峰[1] 王楠[1]
机构地区:[1]兰州军区总医院泌尿外科,甘肃兰州730050
出 处:《现代泌尿外科杂志》2010年第3期207-209,共3页Journal of Modern Urology
摘 要:目的探讨女性重复尿道并泌尿生殖系多发畸形的临床特征及诊治方法。方法总结1例女性重复尿道并泌尿生殖系多发畸形的临床资料。检索Pubmed和CNKI数据库相关文献进行复习。结果病例系临床罕见多系统、器官合并畸形,因生殖器官发育差,诊断欠明确,定期随访。检索结果表明相似文献报道少见,并多合并其他泌尿生殖系畸形。结论女性尿道重复在泌尿系畸形中比较罕见。诊断时详尽的体格检查至关重要,在此基础上行针对性辅助检查,检查应以无创检查为主。根据解剖情况及临床表现行相应的治疗。Objective To discuss the clinical features and treatment of urethral duplication. Methods An unusual case of urethral duplication was reported. The patient was a 2.25-year-old female,complaining of pubic symphysis separation, and perineal deformity. Physical examination showed she had bladder, urethral, and vaginal duplication. Related literature was searched in the Pubmed and CNKI database and the clinical data were reviewed. Results Urethral duplication was a rare anomaly occurring predominantly in males and often associated with other abnormalities in the genitourinary. However, this case was a female with multi-system and multi-organ malformation. Because of the poor genital dvelopment, the diagnosis was not clear yet and regular follow-up was needed. Conclusion Urethral duplication rarely occurred in female. Careful and non-invasive physical examination is essential for the diagnosis. The treatment sholud be based on anatomic and clinical manifestations.
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