The Comprehensive Center for Congenital Adrenal Hyperplasia, New York-Presbyterian Hospital/Weill Cornell Medicine, New York, NY, USA.
Children's Hospital Colorado, Aurora, CO, USA.
J Pediatr Urol. 2018 Apr;14(2):157.e1-157.e8. doi: 10.1016/j.jpurol.2017.11.019. Epub 2018 Feb 2.
Prior studies of outcomes following genitoplasty have reported high rates of surgical complications among children with atypical genitalia. Few studies have prospectively assessed outcomes after contemporary surgical approaches.
The current study reported the occurrence of early postoperative complications and of cosmetic outcomes (as rated by surgeons and parents) at 12 months following contemporary genitoplasty procedures in children born with atypical genitalia.
This 11-site, prospective study included children aged ≤2 years, with Prader 3-5 or Quigley 3-6 external genitalia, with no prior genitoplasty and non-urogenital malformations at the time of enrollment. Genital appearance was rated on a 4-point Likert scale. Paired t-tests evaluated differences in cosmesis ratings.
Out of 27 children, 10 were 46,XY patients with the following diagnoses: gonadal dysgenesis, PAIS or testosterone biosynthetic defect, severe hypospadias and microphallus, who were reared male. Sixteen 46,XX congenital adrenal hyperplasia patients were reared female and one child with sex chromosome mosaicism was reared male. Eleven children had masculinizing genitoplasty for penoscrotal or perineal hypospadias (one-stage, three; two-stage, eight). Among one-stage surgeries, one child had meatal stenosis (minor) and one developed both urinary retention (minor) and urethrocutaneous fistula (major) (Summary Figure). Among two-stage surgeries, three children developed a major complication: penoscrotal fistula, glans dehiscence or urethral dehiscence. Among 16 children who had feminizing genitoplasty, vaginoplasty was performed in all, clitoroplasty in nine, external genitoplasty in 13, urethroplasty in four, perineoplasty in five, and total urogenital sinus mobilization in two. Two children had minor complications: one had a UTI, and one had both a mucosal skin tag and vaginal mucosal polyp. Two additional children developed a major complication: vaginal stenosis. Cosmesis scores revealed sustained improvements from 6 months post-genitoplasty, as previously reported, with all scores reported as good or satisfied.
In these preliminary data from a multi-site, observational study, parents and surgeons were equally satisfied with the cosmetic outcomes 12 months after genitoplasty. A small number of patients had major complications in both feminizing and masculinizing surgeries; two-stage hypospadias repair had the most major complications. Long-term follow-up of patients at post-puberty will provide a better assessment of outcomes in this population.
In this cohort of children with moderate to severe atypical genitalia, preliminary data on both surgical and cosmetic outcomes were presented. Findings from this study, and from following these children in long-term studies, will help guide practitioners in their discussions with families about surgical management.
先前研究报告称,具有非典型生殖器的儿童在接受生殖器成形术后,其手术并发症发生率较高。但鲜有研究前瞻性地评估了当代手术方法后的结局。
本研究报道了在具有非典型生殖器的儿童中,接受当代生殖器成形术后 12 个月时早期术后并发症和美容结局(由外科医生和家长评估)的发生情况。
本 11 个地点、前瞻性研究纳入了≤2 岁、具有 Prader 3-5 级或 Quigley 3-6 级外生殖器、入组时无既往生殖器成形术且无泌尿生殖系统畸形的儿童。生殖器外观采用 4 分李克特量表进行评分。配对 t 检验评估了美容效果评分的差异。
27 名儿童中,10 名是 46,XY 患儿,其诊断为:性腺发育不全、PAIS 或睾酮生物合成缺陷、严重尿道下裂和小阴茎,这些患儿被男性抚养。16 名 46,XX 先天性肾上腺皮质增生症患儿被女性抚养,1 名性染色体嵌合体患儿被男性抚养。11 名儿童接受了阴茎阴囊或会阴型尿道下裂的男性化生殖器成形术(一期手术 3 例;二期手术 8 例)。在一期手术中,1 例患儿发生尿道狭窄(轻度),1 例患儿发生尿潴留(轻度)和尿道皮肤瘘(重度)(汇总图)。在二期手术中,3 例患儿发生严重并发症:阴茎阴囊瘘、龟头裂开或尿道裂开。在接受女性化生殖器成形术的 16 名儿童中,所有患儿均接受了阴道成形术,9 例行阴蒂成形术,13 例行外生殖器成形术,4 例行尿道成形术,5 例行会阴成形术,2 例行全泌尿生殖窦松解术。2 名患儿发生轻度并发症:1 例患儿发生尿路感染,1 例患儿发生黏膜皮赘和阴道黏膜息肉。另外 2 名患儿发生严重并发症:阴道狭窄。如先前报道的那样,美容效果评分从生殖器成形术后 6 个月开始持续改善,所有评分均报告为良好或满意。
在这项来自多中心、观察性研究的初步数据中,家长和外科医生对生殖器成形术后 12 个月的美容效果同样满意。少数患者在男性化和女性化手术中均发生严重并发症;二期尿道下裂修复术的严重并发症最多。对青春期后患者的长期随访将更好地评估该人群的结局。
在本研究中,对具有中重度非典型生殖器的儿童进行了手术和美容结局的初步评估。该研究结果以及对这些患儿的长期研究结果,将有助于指导临床医生与患儿家长讨论手术治疗方案。