Post-operative complications following feminizing genitoplasty in moderate to severe genital atypia: Results from a multicenter, observational prospective cohort study

Disorders/differences of sex development (DSD) are congenital conditions in which there is atypical chromosomal, gonadal and/or phenotypic sex. While there remains controversy around the traditionally binary concept of sex, most patients with DSD are reared either male or female depending on their g...

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Veröffentlicht in:Journal of pediatric urology 2020-10, Vol.16 (5), p.568-575
Hauptverfasser: Baskin, Avi, Wisniewski, Amy B., Aston, Christopher E., Austin, Paul, Chan, Yee-Ming, Cheng, Earl Y., Diamond, David A., Fried, Allyson, Kolon, Thomas, Lakshmanan, Yegappan, Williot, Pierre, Meyer, Sabrina, Meyer, Theresa, Kropp, Bradley, Nokoff, Natalie, Palmer, Blake, Paradis, Alethea, Poppas, Dix, VanderBrink, Brian, Scott Reyes, Kristy J., Tishelman, Amy, Wolfe-Christensen, Cortney, Yerkes, Elizabeth, Mullins, Larry L., Baskin, Laurence
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container_end_page 575
container_issue 5
container_start_page 568
container_title Journal of pediatric urology
container_volume 16
creator Baskin, Avi
Wisniewski, Amy B.
Aston, Christopher E.
Austin, Paul
Chan, Yee-Ming
Cheng, Earl Y.
Diamond, David A.
Fried, Allyson
Kolon, Thomas
Lakshmanan, Yegappan
Williot, Pierre
Meyer, Sabrina
Meyer, Theresa
Kropp, Bradley
Nokoff, Natalie
Palmer, Blake
Paradis, Alethea
Poppas, Dix
VanderBrink, Brian
Scott Reyes, Kristy J.
Tishelman, Amy
Wolfe-Christensen, Cortney
Yerkes, Elizabeth
Mullins, Larry L.
Baskin, Laurence
description Disorders/differences of sex development (DSD) are congenital conditions in which there is atypical chromosomal, gonadal and/or phenotypic sex. While there remains controversy around the traditionally binary concept of sex, most patients with DSD are reared either male or female depending on their genetic sex, gonadal sex, genital phenotype and status of their internal genital tract. This study uses prospective data from 12 institutions across the United States that specialize in DSD care. We focused on patients raised female. Eligible patients had moderate to severe genital atypia (defined as Prader score >2), were ≤2 years of age at entry, and had no prior genitoplasty. The aim of this study is to describe early post operative complications for young patients undergoing modern approaches to feminizing genitoplasty. Of the 91 participants in the cohort, 57 (62%) were reared female. The majority had congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (n = 52), 1 had ovo-testicular syndrome, 2 had mixed gonadal dysgenesis and 2 had partial androgen insensitivity syndrome (PAIS). Of the 50 participants who received early genitoplasty, 43 (86%) had follow-up at 6–12 months post-surgery. Thirty-two participants (64%) received a clitoroplasty, 31 (62%) partial urogenital mobilization and 4 (8%) total urogenital sinus mobilization. Eighteen percent (9/50) experienced post-surgical complications with 7 (14%) being rated as Clavien-Dindo grade III. Both parents and surgeons reported improved satisfaction with genital appearance of participants following surgery compared to baseline. This information on post-operative complications associated with contemporary approaches to feminizing genitoplasty performed in young children will help guide families when making decisions about whether or not to proceed with surgery for female patients with moderate to severe genital atypia. [Display omitted]
doi_str_mv 10.1016/j.jpurol.2020.05.166
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While there remains controversy around the traditionally binary concept of sex, most patients with DSD are reared either male or female depending on their genetic sex, gonadal sex, genital phenotype and status of their internal genital tract. This study uses prospective data from 12 institutions across the United States that specialize in DSD care. We focused on patients raised female. Eligible patients had moderate to severe genital atypia (defined as Prader score &gt;2), were ≤2 years of age at entry, and had no prior genitoplasty. The aim of this study is to describe early post operative complications for young patients undergoing modern approaches to feminizing genitoplasty. Of the 91 participants in the cohort, 57 (62%) were reared female. The majority had congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (n = 52), 1 had ovo-testicular syndrome, 2 had mixed gonadal dysgenesis and 2 had partial androgen insensitivity syndrome (PAIS). Of the 50 participants who received early genitoplasty, 43 (86%) had follow-up at 6–12 months post-surgery. Thirty-two participants (64%) received a clitoroplasty, 31 (62%) partial urogenital mobilization and 4 (8%) total urogenital sinus mobilization. Eighteen percent (9/50) experienced post-surgical complications with 7 (14%) being rated as Clavien-Dindo grade III. Both parents and surgeons reported improved satisfaction with genital appearance of participants following surgery compared to baseline. This information on post-operative complications associated with contemporary approaches to feminizing genitoplasty performed in young children will help guide families when making decisions about whether or not to proceed with surgery for female patients with moderate to severe genital atypia. 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subjects Atypical genitalia
Congenital adrenal hyperplasia
Disorders of sex development
Urogenital sinus reconstruction
title Post-operative complications following feminizing genitoplasty in moderate to severe genital atypia: Results from a multicenter, observational prospective cohort study
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