Mićić S, Papić N, Mladenović I, Prorocić M, Genbacev O
Medical Faculty Clinic of Urology, Zvezdara Clinic and Hospital Centre, Belgrade, Yugoslavia.
Hum Reprod. 1990 Jul;5(5):582-5. doi: 10.1093/oxfordjournals.humrep.a137149.
Congenital absence of both vas deferens accounts for approximately 10% of cases of obstructive azoospermia. The purpose of the present study was to develop a treatment protocol for a group of azoospermic patients using surgical implantation of alloplastic spermatocoele to enable repeated sperm cell aspiration. Nine patients with congenital absence of both vas deferens, two with obstructed and one with destroyed vas, underwent surgery for the implantation of an alloplastic spermatocoele. In 10 of the 12 patients, vital spermatozoa were recovered from the aspirate and used for intrauterine insemination of their female partners with induced ovulation, some of whom then conceived.
双侧输精管先天性缺如约占梗阻性无精子症病例的10%。本研究的目的是为一组无精子症患者制定一种治疗方案，采用同种异体精子囊肿手术植入法，以便能够反复抽吸精子细胞。9例双侧输精管先天性缺如患者、2例输精管梗阻患者和1例输精管毁损患者接受了同种异体精子囊肿植入手术。12例患者中有10例从抽吸物中获取了有活力的精子，并用于对其女性伴侣进行诱导排卵后的宫腔内人工授精，其中一些女性随后受孕。
