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童年期隐睾症手术后仍存在的不育症,可根据促卵泡激素正常或升高的患者进行分类,并在睾丸固定术中得以识别。

Infertility despite surgery for cryptorchidism in childhood can be classified by patients with normal or elevated follicle-stimulating hormone and identified at orchidopexy.

作者信息

Cortes D, Thorup J, Lindenberg S, Visfeldt J

机构信息

Department of Paediatric Surgery, Rigshospitalet, University of Copenhagen, Denmark.

出版信息

BJU Int. 2003 May;91(7):670-4. doi: 10.1046/j.1464-410x.2003.04177.x.

Abstract

OBJECTIVE

To analyse infertility despite orchidopexy in childhood.

PATIENTS AND METHODS

The study comprised patients with cryptorchidism (70 bilateral and 65 unilateral) who had a simultaneous biopsy taken at orchidopexy in childhood, and in adulthood had analyses of semen and FSH. In adulthood 42 formerly bilateral cryptorchid boys had repeat testicular biopsies taken. Infertility was suspected in men with < 5 million sperm/mL in the best sample of semen and concomitant poor sperm motility, and who were classified by follicle-stimulating hormone (FSH) values. At orchidopexy the number of spermatogonia/tubule and the germ cell differentiation were measured. In adulthood the percentage of tubules with complete spermatogenesis, spermatogenic arrest and Sertoli-cell only status was assessed.

RESULTS

Infertility was suspected in 38 of 70 (54%) of formerly bilateral and six of 65 (9%) formerly unilateral cryptorchid patients. High FSH values were expected in these suspected infertile patients, but 15 of 38 (59%) formerly bilateral and five of six formerly unilateral cryptorchid patients had normal FSH values. These patients were identified in childhood at orchidopexy; those with bilateral cryptorchidism generally presented with germ cells, but the mean number of spermatogonia per tubule was < 30% of the lowest normal value, and the germ cells were seldom normally differentiated, whereas those with unilateral cryptorchidism generally lacked germ cells in the biopsies. No patients had a decreased FSH value.

CONCLUSION

Despite surgery for cryptorchidism, infertility was probable in a third (44 of 135) of the patients. We expected high FSH values in these patients, but in 45% (20/44) the FSH values were normal. These patients may have relative FSH deficiency. At orchidopexy these patients were identified to be bilaterally cryptorchid with few germ cells and those unilaterally cryptorchid had none in the biopsy. After orchidopexy in childhood, additional hormonal treatment, e.g. recombinant FSH or buserelin, may be indicated in these patients.

摘要

目的

分析儿童期睾丸固定术后仍存在的不育情况。

患者与方法

本研究纳入了患有隐睾症的患者(70例双侧隐睾和65例单侧隐睾),这些患者在儿童期进行睾丸固定术时同时接受了活检,并在成年期进行了精液和促卵泡生成素(FSH)分析。成年期,42例曾患双侧隐睾的男孩接受了重复睾丸活检。精液最佳样本中精子浓度<500万/mL且精子活力差,并根据促卵泡生成素(FSH)值进行分类的男性被怀疑患有不育症。在睾丸固定术时,测量每曲细精管中生精细胞的数量和生殖细胞分化情况。成年期,评估具有完全生精、生精停滞和仅支持细胞状态的曲细精管百分比。

结果

70例曾患双侧隐睾的患者中有38例(54%)以及65例曾患单侧隐睾的患者中有6例(9%)被怀疑患有不育症。这些疑似不育的患者预计FSH值会升高,但38例曾患双侧隐睾的患者中有15例(59%)以及6例曾患单侧隐睾的患者中有5例FSH值正常。这些患者在儿童期睾丸固定术时被识别出来;双侧隐睾患者通常存在生殖细胞,但每曲细精管中生精细胞的平均数量<最低正常值的30%,且生殖细胞很少正常分化,而单侧隐睾患者活检中通常缺乏生殖细胞。没有患者FSH值降低。

结论

尽管进行了隐睾症手术,但三分之一(135例中的44例)的患者仍有可能不育。我们预计这些患者FSH值会升高,但45%(20/44)的患者FSH值正常。这些患者可能存在相对FSH缺乏。在睾丸固定术时这些患者被识别为双侧隐睾且生殖细胞少,单侧隐睾患者活检中无生殖细胞。儿童期睾丸固定术后,这些患者可能需要额外的激素治疗,如重组FSH或布舍瑞林。

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