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先天性单侧输精管缺如伴梗阻性无精子症的临床特征及显微外科重建: 三级医疗中心经验。

Clinical features and microsurgical reconstruction of congenital unilateral absence of the vas deferens with obstructive azoospermia: a tertiary care center experience.

机构信息

Department of Andrology, The Center for Men's Health, Urologic Medical Center, Shanghai General Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200080, China.

Department of Urology, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai 519000, China.

出版信息

Asian J Androl. 2023 Jan-Feb;25(1):73-77. doi: 10.4103/aja20225.

DOI:10.4103/aja20225
PMID:35381699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9933956/
Abstract

Patients with congenital unilateral absence of the vas deferens (CUAVD) manifest diverse symptoms from normospermia to azoospermia. Treatment for CUAVD patients with obstructive azoospermia (OA) is complicated, and there is a lack of relevant reports. In this study, we describe the clinical features and evaluate the treatments and outcomes of CUAVD patients with OA. From December 2015 to December 2020, 33 patients were diagnosed as CUAVD with OA in Shanghai General Hospital (Shanghai, China). Patient information, ultrasound findings, semen analysis, hormone profiles, and treatment information were collected, and the clinical outcomes were evaluated. Of 33 patients, 29 patients were retrospectively analyzed. Vasoepididymostomy (VE) or cross VE was performed in 12 patients, the patency rate was 41.7% (5/12), and natural pregnancy was achieved in one of the patients. The other 17 patients underwent testicular sperm extraction as the distal vas deferens (contralateral side) was obstructed. These findings showed that VE or cross VE remains an alternative treatment for CUAVD patients with OA, even with a relatively low rate of patency and natural pregnancy.

摘要

先天性单侧输精管缺如(CUAVD)患者的表现从正常精子症到无精子症不等。对于梗阻性无精子症(OA)的 CUAVD 患者的治疗较为复杂,且相关报道较少。本研究旨在描述 CUAVD-OA 患者的临床特征,并评估其治疗方法和结局。2015 年 12 月至 2020 年 12 月,上海交通大学医学院附属上海儿童医学中心共诊断 33 例 CUAVD-OA 患者。收集了患者的信息、超声检查结果、精液分析、激素水平和治疗信息,并评估了临床结局。在 33 例患者中,回顾性分析了 29 例。12 例行输精管附睾吻合术(VE)或交叉 VE,吻合通畅率为 41.7%(5/12),其中 1 例自然妊娠。17 例患者因对侧输精管梗阻而行睾丸精子抽吸术,这些结果表明 VE 或交叉 VE 仍然是 CUAVD-OA 患者的一种替代治疗方法,尽管吻合通畅率和自然妊娠率相对较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fac5/9933956/11938eb5989b/AJA-25-73-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fac5/9933956/11938eb5989b/AJA-25-73-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fac5/9933956/11938eb5989b/AJA-25-73-g001.jpg

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本文引用的文献

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Genetics of Azoospermia.无精子症的遗传学。
Int J Mol Sci. 2021 Mar 23;22(6):3264. doi: 10.3390/ijms22063264.
2
Prevalence of CBAVD in azoospermic men carrying pathogenic CFTR mutations - Evaluated in a cohort of 639 non-vasectomized azoospermic men.携带致病性 CFTR 突变的非阻塞性无精子症男性中 CBAVD 的患病率-在 639 名非输精管结扎的非阻塞性无精子症男性队列中评估。
Andrology. 2021 Mar;9(2):588-598. doi: 10.1111/andr.12925. Epub 2020 Nov 7.
3
A modified single-armed microsurgical vasoepididymostomy for epididymal obstructive azoospermia: intraoperative choice and postoperative consideration.
改良单臂显微吻合术治疗附睾梗阻性无精子症:术中选择和术后考虑。
BMC Urol. 2020 Aug 12;20(1):121. doi: 10.1186/s12894-020-00692-5.
4
Mutation analysis of the cystic fibrosis transmembrane conductance regulator gene in Chinese congenital absence of vas deferens patients.对中国先天性输精管缺失患者的囊性纤维化跨膜电导调节因子基因进行突变分析。
Gene. 2021 Jan 10;765:145045. doi: 10.1016/j.gene.2020.145045. Epub 2020 Aug 8.
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Genetics of the congenital absence of the vas deferens.先天性输精管缺失的遗传学研究。
Hum Genet. 2021 Jan;140(1):59-76. doi: 10.1007/s00439-020-02122-w. Epub 2020 Feb 5.
6
Modified stepwise mini-incision microdissection testicular sperm extraction: a useful technique for patients with a history of orchidopexy affected by non-obstructive azoospermia.改良分步式小切口微创睾丸精子提取术:既往行隐睾固定术的非梗阻性无精子症患者的有效治疗技术。
J Zhejiang Univ Sci B. 2020;21(1):87-92. doi: 10.1631/jzus.B1900232.
7
Male partners of infertile couples with congenital unilateral absence of the vas deferens are mainly non-azoospermic.先天性单侧输精管缺失的不育夫妇的男性伴侣主要是非无精症。
Andrology. 2020 May;8(3):645-653. doi: 10.1111/andr.12749. Epub 2020 Jan 7.
8
Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles.扩展携带 CFTR 和 ADGRG2 等位基因的先天性输精管缺失中国患者的表型和遗传谱。
Andrology. 2019 May;7(3):329-340. doi: 10.1111/andr.12592. Epub 2019 Feb 27.
9
CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of observational studies.CFTR 变体与先天性单侧输精管缺如(CUAVD)男性的肾脏异常:观察性研究的系统评价和荟萃分析。
Genet Med. 2019 Apr;21(4):826-836. doi: 10.1038/s41436-018-0262-7. Epub 2018 Sep 14.
10
The role of vasoepididymostomy for treatment of obstructive azoospermia in the era of in vitro fertilization : a systematic review and meta-analysis.在体外受精时代,输精管附睾吻合术治疗梗阻性无精子症的作用:一项系统评价和荟萃分析。
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