Terrone C, Ceratti G, Bonazzi A, Rocca Rossetti S, Bianchi M
Clinica Urologica dell'Università di Torino.
Arch Ital Urol Androl. 1996 Dec;68(5):353-7.
About 10% of the cases of male infertility is represented by the obstruction of the seminal tract, which may be congenital or secondary to inflammatory events or surgery. The most frequent obstructive malformation of the seminal tract is the bilateral agenesia of the vas deferens. Such malformation is typical of the cystic fibrosis (CF), an autosomal recessive disorder determining chronic respiratory infections with bronchiectasia, and pancreatic failure. Recently the defective gene responsible for CF has been identified on the long arm of the chromosome 7. Congenital bilateral absence of the vas deferens (CBAVD) may be present in otherwise healthy males without clinical evidence of CF. Genetics studies demonstrated that most CBAVD display at least one detectable CF mutation, therefore this disease can be considered as an incomplete clinical form of CF. With the realization that a man with CBAVD may have CF, albeit a genital form, considerable care is required not only to document his specific mutations, but also to test his partner for CF mutations to evaluate the risk that their child would have CF. The association of chronic suppurating respiratory disease with obstructive azoospermia characterizes also the Young's syndrome. In this disease the obstruction could possibly be the result of defective epididymal sperm transport, related to an abnormality in the mucus. Despite some clinical common aspects, CF and Young's syndrome are two distinct entity. In fact, no CF mutations have been demonstrated in Young's syndrome. Congenital obstructive abnormalities of the vas deferens and epididymis are often associate to cryptorchidism (36-68% of the cases) and to patent processus vaginalis. The degree of testicular retention and processus vaginalis closure correlates well with the incidence of associated epididymal defects. Rare causes of congenital obstructive azoospermia are represent by the cyst of Müllerian or Wolffian origin. An obstruction to the progression of the sperm along the seminal tract can also be present in complex malformations, such as pseudohermaphroditism in which the infertility has a multifactorial etiology.
男性不育病例中约10%是由输精管道梗阻引起的,其可能是先天性的,或继发于炎症事件或手术。输精管道最常见的梗阻性畸形是双侧输精管缺如。这种畸形是囊性纤维化(CF)的典型表现,CF是一种常染色体隐性疾病,可导致慢性呼吸道感染伴支气管扩张以及胰腺功能衰竭。最近,导致CF的缺陷基因已在7号染色体长臂上被确定。先天性双侧输精管缺如(CBAVD)可能出现在其他方面健康、无CF临床证据的男性中。遗传学研究表明,大多数CBAVD至少有一个可检测到的CF突变,因此这种疾病可被视为CF的一种不完全临床形式。鉴于认识到患有CBAVD的男性可能患有CF,尽管是生殖器形式,不仅需要谨慎记录其特定突变,还需要检测其伴侣是否有CF突变,以评估他们的孩子患CF的风险。慢性化脓性呼吸道疾病与梗阻性无精子症的关联也是杨氏综合征的特征。在这种疾病中,梗阻可能是附睾精子运输缺陷的结果,与黏液异常有关。尽管有一些临床共同特征,但CF和杨氏综合征是两种不同的疾病实体。事实上,杨氏综合征中未发现CF突变。输精管和附睾的先天性梗阻异常常与隐睾症(36 - 68%的病例)和鞘状突未闭有关。睾丸下降不全程度和鞘状突闭合情况与相关附睾缺陷的发生率密切相关。先天性梗阻性无精子症的罕见原因是苗勒管或中肾管来源的囊肿。精子沿输精管道前行的梗阻也可能存在于复杂畸形中,如两性畸形,其中不育具有多因素病因。