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大型卵睾性生殖器发育障碍患者队列的长期随访。

Long-term followup of a large cohort of patients with ovotesticular disorder of sex development.

机构信息

Division of Urology, Hospital das Clínicas, School of Medicine, University of São Paulo, São Paulo, Brazil; Division of Endocrinology, Hospital das Clínicas, School of Medicine, University of São Paulo, São Paulo, Brazil.

Division of Urology, Hospital das Clínicas, School of Medicine, University of São Paulo, São Paulo, Brazil.

出版信息

J Urol. 2014 May;191(5 Suppl):1532-6. doi: 10.1016/j.juro.2013.10.037. Epub 2014 Mar 26.

Abstract

PURPOSE

We present the followup of a large cohort of patients with ovotesticular disorder of sex development treated at a single tertiary center.

MATERIALS AND METHODS

We reviewed the records of 20 patients with ovotesticular disorder of sex development. We retrospectively evaluated clinical and surgical characteristics. A prospective study was also performed, including evaluation of surgical results, gonadal function, sexual activity and voiding symptoms of these patients during adulthood.

RESULTS

All patients had ambiguous genitalia, including 18 with a 46,XX karyotype and 2 with a 46,XX/46,XY karyotype. Gender assignment at birth was male in 13 patients and female in 7. Three females were later reassigned to the male gender. Bilateral gonadectomy was performed in 10 patients. Testicular tissue was preserved in 8 males and ovarian tissue was preserved in 2 females. Average followup was 25 years (range 4 to 46). Puberty started spontaneously in 14 patients between ages 11 and 14 years. Seven patients showed spontaneous puberty after conservative gonadal surgery and 4 required hormonal replacement during adulthood. The most frequent complications in males were urethral fistula in 6 and late urethral stenosis in 3. Two patients with urethral stenosis had symptoms 10 years postoperatively. One female presented with temporary dyspareunia. In adulthood 8 males and 2 females reported sexual activity. All male patients reported orgasm and 2 reported ejaculation.

CONCLUSIONS

Male gender assignment was more prevalent. Long-term followup revealed adequate pubertal development and sexual activity. Complications involving the urethra developed frequently in male patients.

摘要

目的

我们介绍了在一家三级中心接受治疗的一大群卵睾性性发育障碍患者的随访结果。

材料与方法

我们回顾了 20 例卵睾性性发育障碍患者的记录。我们回顾性评估了临床和手术特征。还进行了一项前瞻性研究,包括评估这些成年患者的手术结果、性腺功能、性行为和排尿症状。

结果

所有患者的外生殖器均存在两性畸形,其中 18 例核型为 46,XX,2 例核型为 46,XX/46,XY。出生时性别分配为男性 13 例,女性 7 例。3 例女性后来被重新分配为男性。10 例患者行双侧性腺切除术。8 例男性保留了睾丸组织,2 例女性保留了卵巢组织。平均随访时间为 25 年(范围 4 至 46 年)。14 例患者在 11 至 14 岁之间自然开始青春期。7 例患者在保留性腺手术后自发出现青春期,4 例患者在成年后需要激素替代治疗。男性最常见的并发症是 6 例尿道瘘和 3 例迟发性尿道狭窄。2 例尿道狭窄患者在术后 10 年出现症状。1 例女性出现暂时性性交困难。成年后,8 例男性和 2 例女性报告有性行为。所有男性患者均报告有性高潮,2 例报告有射精。

结论

男性性别分配更为常见。长期随访显示青春期发育和性行为充分。男性患者常发生涉及尿道的并发症。

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