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患有 46,XX 和先天性肾上腺增生的明显男性化患者是否应考虑男性性别分配?

Should male gender assignment be considered in the markedly virilized patient With 46,XX and congenital adrenal hyperplasia?

机构信息

Section of Pediatric Endocrinology, Riley Hospital for Children, Indiana University School of Medicine, Indianapolis, Indiana, USA.

出版信息

J Urol. 2010 Oct;184(4 Suppl):1786-92. doi: 10.1016/j.juro.2010.03.116. Epub 2010 Aug 21.

Abstract

PURPOSE

We assess the outcome in 46,XX men with congenital adrenal hyperplasia who were born with Prader 4 or 5 genitalia and assigned male gender at birth.

MATERIALS AND METHODS

After receiving institutional review board approval and subject consent we reviewed the medical records of 12 men 35 to 69 years old with 46,XX congenital adrenal hyperplasia, of whom 6 completed social and gender issue questionnaires.

RESULTS

All subjects were assigned male gender at birth, were diagnosed with virilizing congenital adrenal hyperplasia at age greater than 3 years and indicated a male gender identity with sexual orientation to females. Ten of the 12 subjects had always lived as male and 2 who were reassigned to female gender in childhood subsequently self-reassigned as male. Nine of the 12 men had long-term female partners, including 7 married 12 years or more. The 3 subjects without a long-term female partner included 1 priest, 1 who was reassigned female gender, married, divorced and self-reassigned as male, and 1 with a girlfriend and sexual activity. All except the priest and the subject who was previously married when female indicated a strong libido and frequent orgasmic sexual activity. Responses to self-esteem, masculinity, body image, social adjustment and symptom questionnaires suggested adjustments related to the extent of familial and social support.

CONCLUSIONS

Outcome data on severely masculinized 46,XX patients with congenital adrenal hyperplasia who were assigned male gender at birth indicate male gender identity in adulthood with satisfactory male sexual function in those retaining male genitalia. In men who completed questionnaires results were poorer in those lacking familial/social support. Male gender of rearing may be a viable option for parents whose children are born with congenital adrenal hyperplasia, a 46,XX karyotype and male genitalia, although positive parental and other support, and counseling are needed for adjustment.

摘要

目的

我们评估了 46,XX 男性先天性肾上腺皮质增生患者的结局,这些患者出生时具有 Prader4 或 5 型生殖器,出生时被指定为男性性别。

材料和方法

在获得机构审查委员会批准和受试者同意后,我们回顾了 12 名年龄在 35 至 69 岁之间的 46,XX 先天性肾上腺皮质增生男性患者的病历,其中 6 名完成了社会和性别问题问卷。

结果

所有患者均在出生时被指定为男性性别,在 3 岁以上时被诊断为男性化先天性肾上腺皮质增生,并表示具有女性性取向的男性性别认同。12 名受试者中有 10 名一直以男性身份生活,2 名在儿童时期被重新分配为女性性别,随后自行重新分配为男性性别。12 名男性中有 9 名有长期的女性伴侣,其中 7 名结婚 12 年或以上。没有长期女性伴侣的 3 名受试者包括 1 名牧师、1 名以前是女性时被重新分配为女性性别、结婚、离婚并自行重新分配为男性的受试者,以及 1 名有女朋友和性行为的受试者。除了牧师和以前是女性时结婚的受试者外,所有受试者都表示性欲强烈,经常有性高潮的性行为。对自尊、男子气概、身体形象、社会适应和症状问卷的回答表明,调整与家庭和社会支持的程度有关。

结论

对出生时被指定为男性性别、严重男性化的 46,XX 先天性肾上腺皮质增生患者的结局数据表明,成年后具有男性性别认同,保留男性生殖器的患者具有满意的男性性功能。在完成问卷的男性中,缺乏家庭/社会支持的男性结果较差。对于那些孩子出生时患有先天性肾上腺皮质增生、46,XX 染色体核型和男性生殖器的父母来说,男性抚养可能是一个可行的选择,尽管需要积极的父母和其他支持以及咨询来进行调整。

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