Coran A G, Polley T Z
Section of Pediatric Surgery, University of Michigan Medical School, Ann Arbor.
J Pediatr Surg. 1991 Jul;26(7):812-20. doi: 10.1016/0022-3468(91)90146-k.
Proper gender assignment to a neonate born with ambiguous genitalia is a social emergency of the newborn period. Once an appropriate sex assignment has been made, the next critical step is performance, if needed, of a reconstructive procedure in a timely fashion. In an attempt to evaluate our experience with this unique group of patients, we have retrospectively reviewed the course of 69 children with ambiguous genitalia managed surgically at this institution between 1974 and 1989. This series consists of 32 genotypic females with congenital adrenal hyperplasia (CAH), 10 children with mixed gonadal dysgenesis (MGD), 10 male pseudohermaphrodites, 3 true hermaphrodites, 8 genotypic females with urogenital sinus anomalies (UGS), and 6 genotypic males with bilateral undescended testes and penoscrotal hypospadius. All newborns initially seen at this institution received proper sex assignment within the first week of life. Prior to 1980, 17 of the children with CAH underwent clitorectomy and vaginoplasty and three underwent clitoral recession and vaginoplasty. After 1980, 10 patients with CAH were managed with clitoral recession and vaginoplasty and 2 with vaginoplasty alone. Eight of 10 cases of MGD were given a female sex assignment and all 8 underwent gonadectomy due to the high risk of gonadoblastoma; the other 2 children were raised as males. There were 3 true hermaphrodites of which 2 were assigned female gender roles and were managed with a clitoral recession and vaginoplasty. All 10 male pseudohermaphrodites were raised as females and all underwent bilateral orchidectomy. The 8 children with UGS were raised as females and underwent vaginal reconstruction.(ABSTRACT TRUNCATED AT 250 WORDS)
对生殖器模糊的新生儿进行恰当的性别指定是新生儿期的一项社会紧急情况。一旦做出合适的性别指定,接下来关键的一步就是在需要时及时进行重建手术。为了评估我们在这类特殊患者群体中的经验,我们回顾性分析了1974年至1989年间在本机构接受手术治疗的69例生殖器模糊儿童的病程。该系列包括32例患有先天性肾上腺皮质增生症(CAH)的基因型女性、10例混合性性腺发育不全(MGD)儿童、10例男性假两性畸形、3例真两性畸形、8例患有泌尿生殖窦异常(UGS)的基因型女性以及6例患有双侧隐睾和阴茎阴囊型尿道下裂的基因型男性。所有最初在本机构就诊的新生儿在出生后第一周内都接受了恰当的性别指定。1980年之前,17例CAH患儿接受了阴蒂切除术和阴道成形术,3例接受了阴蒂退缩和阴道成形术。1980年之后,10例CAH患者接受了阴蒂退缩和阴道成形术,2例仅接受了阴道成形术。10例MGD病例中有8例被指定为女性性别,由于性腺母细胞瘤风险高,所有8例都接受了性腺切除术;另外2例儿童被当作男性抚养。有3例真两性畸形,其中2例被指定为女性性别角色,并接受了阴蒂退缩和阴道成形术。所有10例男性假两性畸形都被当作女性抚养,均接受了双侧睾丸切除术。8例UGS患儿被当作女性抚养,并接受了阴道重建。(摘要截选至250词)