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作 者:费前进[1] 黄学锋[1] 李澄棣[1] 张李雅[1] 杨旭[1]
机构地区:[1]浙江省温州医学院附属第一医院生殖医学中心,温州325000
出 处:《生殖医学杂志》2009年第2期119-122,共4页Journal of Reproductive Medicine
摘 要:目的探讨无精子症患者的病因。方法对922例无精子症患者按WHO标准进行病因诊断分析。结果922例无精子症患者中先天性异常445例(48.3%)、特发性无精子症206例(22.3%)、梗阻性无精子症198例(21.5%)、医源性疾病26例(2.8%)、获得性睾丸损伤23例(2.5%)、全身性疾病10例(1.1%)、精索静脉曲张8例(0.9%)、内分泌病因6例(0.7%);206例特发性无精子症患者睾丸活检结果,睾丸生精功能低下38例(18.4%)、生精阻滞69例(33.5%)、唯支持细胞综合征(SCOS)90例(43.7%)、生精小管透明变性9例(4.4%)。结论先天性异常、特发性无精子症和梗阻性无精子症是无精子症患者的主要病因,SCOS是特发性无精子症患者睾丸生精障碍的主要病理类型。Objective.To investigate the etiology of the patients with azoospermia. Methods:Nine hundred and twenty-two patients with diagnosed azoospermia were classified according to the WHO manual. Results:Of 922 patients, 445 were diagnosed as congenital abnormalities (48.3%), 206 as idiopathic azoospermia (22.3%), 198 as obstructive azoospermia (21.5%), 26 as iatrogenic causes (2.8%), 23 as acquired testicular damage (2. 5%), 10 as systemic causes (1. 1%), 8 as varicocele (0. 9%), and 6 as endocrine causes (0. 7%). Testicular biopsy was performed on 206 patients diagnosed with idiopathic azoospermia, and the histopathological results showed that there were 38 patients (18. 4%) with hypospermatogenesis, 69 (33.5%) with maturation arrest, 90 (43.7%) with Sertoli cell-only syndrome (SCOS) and 9 (4.4%) with seminiferous tubule hyalinization. Conclusions: Congenital abnormalities, idiopathic azoospermia and obstructive azoospermia were the main causes of azoospermia, and the main testicular problem in the patients with idiopathic azoospermia was SCOS.
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