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先天性肾上腺增生症的外科治疗

Surgical treatment of congenital adrenal hyperplasia.

作者信息

Schnitzer J J, Donahoe P K

机构信息

Pediatric Surgical Services and Pediatric Surgical Research Laboratories, Massachusetts General Hospital, Boston, Massachusetts, USA.

出版信息

Endocrinol Metab Clin North Am. 2001 Mar;30(1):137-54. doi: 10.1016/s0889-8529(08)70023-9.

Abstract

Unraveling of the genetics of CAH offers the possibility of earlier detection and prenatal treatment or, alternatively, blastocyst embryo selection and eventually in utero gene therapy. Endocrine, surgical, and anesthesia management after birth have improved, leading to a better outcome for these patients. In the authors' experience, early one-stage reconstructive surgery, although demanding, allows one to use all available tissue. Once mastered, the repair is actually technically easier than vaginal pull-through surgery in the adolescent. Patients go through childhood with a body image that is more concordant with normal. Neither the child nor the parents must suffer the anticipation of a major operative intervention at puberty that can cause great emotional stress and that may be more difficult. The authors have encountered situations in late adolescence in which it has been impossible to separate the urogenital sinus from below. Under these circumstances, one can consider a posterior sagittal approach in which the rectum is bivalved to allow one to approach the vagina from below in an attempt to separate it safely from the urethra and to mobilize it to the perineum. It is also feasible to consider fashioning a segment of sigmoid colon as a neovagina, realizing that mucosal drainage needs to be managed daily. The authors have also encountered the rare 46,XX patient raised as a male and committed to the male role. In these cases, the patient can be offered gonadectomy, followed by staged complex hypospadias repair, and surgery to remove Müllerian structures and, if possible, to preserve the vas, followed by prepenile scrotal repair and insertion of testicular prostheses. Children with CAH require a lifetime of care with surgical approaches that are age appropriate. These patients can lead a full and productive life. It is the physician's responsibility to make certain that these children reach their full potential with the least number of interventions, which should be designed and optimized to produce the best possible outcome.

摘要

对先天性肾上腺皮质增生症(CAH)遗传学的深入研究为早期检测和产前治疗提供了可能,或者也可以选择囊胚胚胎筛选,最终实现子宫内基因治疗。出生后的内分泌、外科和麻醉管理已经得到改善,这些患者的预后也更好。根据作者的经验,早期一期重建手术虽然要求较高,但可以利用所有可用组织。一旦掌握,实际上修复在技术上比青少年期的经阴道拖出手术更容易。患者在童年时期的身体形象与正常人更相符。儿童和父母都不必承受青春期重大手术干预带来的预期压力,这种干预可能会造成巨大的情绪压力,而且可能更困难。作者在青春期后期遇到过无法从下方分离泌尿生殖窦的情况。在这种情况下,可以考虑采用后矢状入路,将直肠一分为二,以便从下方接近阴道,试图将其与尿道安全分离并将其游离至会阴。考虑用一段乙状结肠构建新阴道也是可行的,但要意识到需要每天处理黏膜引流问题。作者还遇到过罕见的46,XX患者,从小被当作男性抚养并承担男性角色。在这些情况下,可以为患者进行性腺切除术,随后分期进行复杂的尿道下裂修复,以及切除苗勒管结构的手术,如果可能的话,保留输精管,然后进行阴茎前阴囊修复和植入睾丸假体。患有CAH的儿童需要一生的护理,手术方法应根据年龄进行调整。这些患者可以过上充实而有意义的生活。医生有责任确保这些孩子以最少的干预发挥最大的潜力,这些干预措施应经过设计和优化,以产生尽可能好的结果。

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