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Y染色体性腺发育不全病例的评估:18年临床经验

The Evaluation of Cases with Y-Chromosome Gonadal Dysgenesis: Clinical Experience over 18 Years.

作者信息

Berberoğlu Merih, Şıklar Zeynep

机构信息

Ankara University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey.

Includes all members from 1996 to 2017.

出版信息

J Clin Res Pediatr Endocrinol. 2018 Mar 1;10(1):30-37. doi: 10.4274/jcrpe.4826. Epub 2017 Aug 21.

Abstract

OBJECTIVE

Y-chromosome gonadal dysgenesis (GD) is a rare subgroup of disorders of sexual development (DSD) which results from underdeveloped testis and may exhibit heterogenous symptoms. These patients are phenotypically classified into two groups - complete and partial, and their karyotypic description is either 46,XY GD or 45,X/46,XY GD. In this study; we aimed to evaluate the characteristics of cases with Y-chromosome GD.

METHODS

Thirty eight cases were followed-up between 1998 and 2016. The age of admission ranged between 0 and 17 years. Clinical and laboratory findings as well as follow-up characteristics of the cases were evaluated retrospectively from the patient files.

RESULTS

There were 26 cases (four complete, 22 partial) in the 46,XY GD group, and 12 cases (four complete, 8 patients with complete GD in the 45,X/46,XY. Mean age at admission was 6.2±4.6 years for all cases. Patients with complete GD in the 45,X/46,XY GD group were diagnosed earlier that the patients with complete GD in the 46,XY group [11 years vs. 14.31 years of age (p<0.01)]. There were no additional findings in 55% of all patients. In the remaining 45% additional clinical findings, mainly short stature, were detected in 75% of the patients in the 45,X/46,XY GD and 30% of the patients in the 46,XY GD groups. All patients with complete 46,XY and 45,X/46,XY GD were raised as females. There was no gender dysphoria in patients that were raised as females, except for one case. Gonadectomy was performed in 14 patients, at a mean age of 8.75±2.3 years and pathological assessment of the gonads was reported as normal in all cases.

CONCLUSION

Y-chromosome GD is a very heterogenous clinical and genetic disorder and requires a multifaceted approach to management. Whether including syndromic features or not, associated clinical features may lead to earlier diagnosis, especially in complete forms of GD. Due to difficulties encountered in the long-term follow-up of these patients, evaluation of appropriateness of sex of rearing decision is not truly possible. Performance of gonadectomy during the first decade appears be a preventive factor for tumor development since these tumors are usually seen during the second decade.

摘要

目的

Y染色体性腺发育不全(GD)是性发育障碍(DSD)中一个罕见的亚组,由睾丸发育不全引起,可能表现出异质性症状。这些患者在表型上分为两组——完全型和部分型,其核型描述为46,XY GD或45,X/46,XY GD。在本研究中,我们旨在评估Y染色体GD病例的特征。

方法

1998年至2016年期间对38例病例进行了随访。入院年龄在0至17岁之间。从患者病历中回顾性评估病例的临床和实验室检查结果以及随访特征。

结果

46,XY GD组有26例(4例完全型,22例部分型),45,X/46,XY组有12例(4例完全型,8例部分型)。所有病例的平均入院年龄为6.2±4.6岁。45,X/46,XY GD组的完全型GD患者比46,XY组的完全型GD患者诊断得更早[11岁对14.31岁(p<0.01)]。55%的所有患者没有其他发现。在其余45%有额外临床发现的患者中,主要是身材矮小,在45,X/46,XY GD组75%的患者和46,XY GD组30%的患者中被检测到。所有46,XY和45,X/46,XY完全型GD患者均按女性抚养。除1例患者外,按女性抚养的患者没有性别焦虑。14例患者进行了性腺切除术,平均年龄为8.75±2.3岁,所有病例性腺的病理评估均报告为正常。

结论

Y染色体GD是一种非常异质的临床和遗传疾病,需要多方面的管理方法。无论是否包括综合征特征,相关的临床特征可能导致更早的诊断,尤其是在完全型GD中。由于这些患者长期随访中遇到困难,真正评估抚养性别决定的适宜性是不可能的。在第一个十年内进行性腺切除术似乎是肿瘤发生的预防因素,因为这些肿瘤通常在第二个十年出现。

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