为什么儿科医生需要了解性发育障碍:709例专业服务的经验

Mayra de Souza El Beck, Carlos W. Germano, Beatriz A. Barros, Juliana G.R. Andrade, Guilherme Guaragna‐Filho, Georgette B. Paula, Márcio L. Miranda, Mara S. Guaragna, Helena Fabbri‐Scallet, Tais N. Mazzola, Nilma L. Viguetti‐Campos, Társis A.P. Vieira, Sofia H.V. Lemos‐Marini, Antonia P. Marques‐de‐Faria, Roberto B. Paiva e Silva, Maricilda P. Mello, Andréa T. Maciel‐Guerra, Gil Guerra‐Júnior
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引用次数: 0

摘要

目的评价性发育障碍(DSD)患者的转诊年龄及其与初诊主诉、转诊时性别、诊断后定义性别及病因诊断的相关性。方法回顾性分析1989 ~ 2016年在某DSD门诊就诊的所有DSD患者的初诊年龄、就诊原因、初社会性别、诊断后性别、核型及病因诊断。不涉及DSD的病例和DSD诊断通常不涉及生殖器模糊,因此不需要专门监测的病例被排除在外。结果1793例患者中,1139例诊断为不同类型的DSD。本研究排除430例(Turner综合征272例,Klinefelter综合征66例,单纯性腺发育不良92例),共纳入709例。其中,82.9%因生殖器模糊而转诊;只有四分之一的儿童仍在生命的第一个月,6.6%的儿童因青春期延迟而转诊,其中大多数年龄在10岁或更大。其中68.6%诊断为XY型DSD, 22.4%诊断为XX型DSD, 9%诊断为性染色体异常。结论:本研究是文献中在单一中心治疗DSD患者的最大系列研究。多数患者的转诊时间不理想,较轻的患者和许多有青春期表现的患者转诊时间更晚。研究结果强调了继续教育专业人员的重要性,这些专业人员主要是儿科医生和新生儿医生,他们将首次接触这些患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Why pediatricians need to know the disorders of sex development: experience of 709 cases in a specialized service

Objective

To evaluate, in a sample of patients with disorders of sex development (DSD), data related to the age at referral and their correlation with the initial complaints, gender at referral, defined gender after diagnosis and etiological diagnosis.

Methods

Retrospective review of the age at the first consultation and the reason for it, initial social gender and gender after the diagnosis, karyotype and etiological diagnosis of all cases treated at a DSD outpatient clinic between 1989 and 2016. Cases that did not involve DSD and DSD diagnoses that do not usually involve ambiguous genitalia, thus not requiring specialized monitoring, were excluded.

Results

Of the 1793 treated cases, 1139 were diagnosed with some type of DSD. This study excluded 430 cases (272 with Turner's syndrome, 66 with Klinefelter syndrome, and 92 with pure gonadal dysgenesis), thus a total 709 individuals were included. Of these, 82.9% were referred due to ambiguous genitalia; only one‐quarter were still in the first month of life, and 6.6% were referred due to pubertal delay, with most of them aged 10 years or older. Of these patients, 68.6% had a diagnosis of XY DSD, 22.4% of XX DSD, and 9% of sex chromosome abnormalities.

Conclusions

This study presents the largest series in the literature of patients with DSD treated in a single center. The time of referral of the majority of patients with ambiguous genitalia fell short of the ideal, and milder cases of ambiguous genitalia and many with pubertal manifestations were referred even later. The results reinforce the importance of continuing education for professionals who will have the first contact with these patients, mainly pediatricians and neonatologists.

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