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卵睾性器官发育障碍的长期预后:单中心经验。

Long-term outcome of ovotesticular disorder of sex development: a single center experience.

机构信息

Department of Urology, Osaka Medical Center and Research Institute for Maternal and Child Health, Izumi, Osaka, Japan.

出版信息

Int J Urol. 2011 Mar;18(3):231-6. doi: 10.1111/j.1442-2042.2010.02700.x. Epub 2011 Jan 23.

Abstract

OBJECTIVES

To describe the clinical features of children with ovotesticular disorder of sex development (DSD) and to review cases of ovotesticular DSD in Japan.

METHODS

Medical records of eight children diagnosed with ovotesticular DSD at our institute during the past 17 years were retrospectively evaluated. A review of 165 reported cases of ovotesticular DSD from Japanese institutions was carried out.

RESULTS

Mean follow up was 8.2 years for six children, with two children lost to follow up. Mean age at first presentation was 2.4 months. All children were Japanese. The most common initial manifestation was ambiguous genitalia. The female:male ratio as the sex of rearing was 1:1. Gender reassignment, from male to female, was carried out in one child at 4-months-old. Genital surgery was always carried out in early childhood as per family desire. Appropriate gonadal tissue was preserved except for one child. No gonadal tumors were detected during follow up. Spontaneous pubertal development occurred in one boy. In reviewing Japanese data, the frequency of testes was higher than in other ethnicities and this was related to the higher incidence of 46,XY.

CONCLUSIONS

According to our experience, most families in Japan desire early genital surgery in the case of ovotesticular DSD. Chromosomal and gonadal distributions in patients with ovotesticular DSD differ between Japanese and other ethnic groups. Treatment for these patients needs to be provided after considering the cultural and social backgrounds of DSD in Japan.

摘要

目的

描述卵睾性性发育障碍(DSD)患儿的临床特征,并复习日本卵睾性 DSD 病例。

方法

回顾性分析我院过去 17 年诊断为卵睾性 DSD 的 8 例患儿的病历资料。对日本机构报告的 165 例卵睾性 DSD 病例进行了复习。

结果

6 例患儿的平均随访时间为 8.2 年,2 例患儿失访。首次就诊时的平均年龄为 2.4 个月。所有患儿均为日本人。最常见的初始表现为外生殖器模糊。按养育性别计算的男女比例为 1:1。1 例患儿在 4 个月大时被性别重置为女性。根据家庭意愿,所有患儿均在幼儿期进行了生殖器手术。除 1 例患儿外,均保留了适当的性腺组织。随访期间未发现性腺肿瘤。1 例男孩出现自发青春期发育。在回顾日本数据时,睾丸的发生率高于其他种族,这与 46,XY 的发生率较高有关。

结论

根据我们的经验,日本的大多数家庭希望在卵睾性 DSD 情况下尽早进行生殖器手术。卵睾性 DSD 患者的染色体和性腺分布在日本和其他种族之间存在差异。在为这些患者提供治疗时,需要考虑日本 DSD 的文化和社会背景。

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