Literature DB >> 27132944

Surgery in disorders of sex development (DSD) with a gender issue: If (why), when, and how?

Pierre D E Mouriquand1, Daniela Brindusa Gorduza2, Claire-Lise Gay2, Heino F L Meyer-Bahlburg3, Linda Baker4, Laurence S Baskin5, Claire Bouvattier6, Luis H Braga7, Anthony C Caldamone8, Lise Duranteau9, Alaa El Ghoneimi10, Terry W Hensle11, Piet Hoebeke12, Martin Kaefer13, Nicolas Kalfa14, Thomas F Kolon15, Gianantonio Manzoni16, Pierre-Yves Mure2, Agneta Nordenskjöld17, J L Pippi Salle18, Dix Phillip Poppas19, Philip G Ransley20, Richard C Rink14, Romao Rodrigo21, Léon Sann22, Justine Schober23, Hisham Sibai24, Amy Wisniewski25, Katja P Wolffenbuttel26, Peter Lee27.   

Abstract

Ten years after the consensus meeting on disorders of sex development (DSD), genital surgery continues to raise questions and criticisms concerning its indications, its technical aspects, timing and evaluation. This standpoint details each distinct situation and its possible management in 5 main groups of DSD patients with atypical genitalia: the 46,XX DSD group (congenital adrenal hyperplasia); the heterogeneous 46,XY DSD group (gonadal dysgenesis, disorders of steroidogenesis, target tissues impairments …); gonosomic mosaicisms (45,X/46,XY patients); ovo-testicular DSD; and "non-hormonal/non chromosomal" DSD. Questions are summarized for each DSD group with the support of literature and the feed-back of several world experts. Given the complexity and heterogeneity of presentation there is no consensus regarding the indications, the timing, the procedure nor the evaluation of outcome of DSD surgery. There are, however, some issues on which most experts would agree: 1) The need for identifying centres of expertise with a multidisciplinary approach; 2) A conservative management of the gonads in complete androgen insensitivity syndrome at least until puberty although some studies expressed concerns about the heightened tumour risk in this group; 3) To avoid vaginal dilatation in children after surgical reconstruction; 4) To keep asymptomatic mullerian remnants during childhood; 5) To remove confirmed streak gonads when Y material is present; 6) It is likely that 46,XY cloacal exstrophy, aphallia and severe micropenis would do best raised as male although this is based on limited outcome data. There is general acknowledgement among experts that timing, the choice of the individual and irreversibility of surgical procedures are sources of concerns. There is, however, little evidence provided regarding the impact of non-treated DSD during childhood for the individual development, the parents, society and the risk of stigmatization. The low level of evidence should lead to design collaborative prospective studies involving all parties and using consensual protocols of evaluation.
Copyright © 2016 Journal of Pediatric Urology Company. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  17β hydroxy steroid dehydrogenase; 17βHSD; 5α reductase deficiency; AIS; Androgen insensitivity syndrome; CAH; Chromosomal anomalies; Congenital adrenal hyperplasia; DSD; Disorders of sex development; Genital surgery in children; Gonadal dysgenesis; Gonadal dysplasia; Hypospadias; Micropenis; Mixed gonadal dysgenesis; Ovo-testicular DSD

Mesh:

Year:  2016        PMID: 27132944     DOI: 10.1016/j.jpurol.2016.04.001

Source DB:  PubMed          Journal:  J Pediatr Urol        ISSN: 1477-5131            Impact factor:   1.830


  36 in total

Review 1.  Disorders/differences of sex development (DSDs) for primary care: the approach to the infant with ambiguous genitalia.

Authors:  Justin A Indyk
Journal:  Transl Pediatr       Date:  2017-10

2.  Introduction to the Special Section: Disorders of Sex Development.

Authors:  David E Sandberg; Vickie Pasterski; Nina Callens
Journal:  J Pediatr Psychol       Date:  2017-06-01

3.  Contemporary Demographic, Treatment, and Geographic Distribution Patterns for Disorders of Sex Development.

Authors:  Rohit Tejwani; Ruiyang Jiang; Steven Wolf; Deanna W Adkins; Brian J Young; Muhammad Alkazemi; John S Wiener; Gina-Maria Pomann; J Todd Purves; Jonathan C Routh
Journal:  Clin Pediatr (Phila)       Date:  2017-07-30       Impact factor: 1.168

Review 4.  Aphallia: a review to standardize management.

Authors:  Tarryn Gabler; Robyn Charlton; Jerome Loveland; Ellen Mapunda
Journal:  Pediatr Surg Int       Date:  2018-04-20       Impact factor: 1.827

5.  Uncertainty and Posttraumatic Stress: Differences Between Mothers and Fathers of Infants with Disorders of Sex Development.

Authors:  Alexandria M Delozier; Kaitlyn L Gamwell; Christina Sharkey; Dana M Bakula; Megan N Perez; Cortney Wolfe-Christensen; Paul Austin; Laurence Baskin; Kerlly J Bernabé; Yee-Ming Chan; Earl Y Cheng; David A Diamond; Rebecca E H Ellens; Allyson Fried; Denise Galan; Saul Greenfield; Thomas Kolon; Bradley Kropp; Yegappan Lakshmanan; Sabrina Meyer; Theresa Meyer; Natalie J Nokoff; Kristy J Reyes; Blake Palmer; Dix P Poppas; Alethea Paradis; Amy C Tishelman; Elizabeth B Yerkes; John M Chaney; Amy B Wisniewski; Larry L Mullins
Journal:  Arch Sex Behav       Date:  2019-05-29

6.  Community perspectives on difference of sex development (DSD) diagnoses: A crowdsourced survey.

Authors:  M Hassan Alkazemi; Ashley W Johnston; Diane Meglin; Deanna Adkins; Jonathan C Routh
Journal:  J Pediatr Urol       Date:  2020-04-27       Impact factor: 1.830

Review 7.  Disorders of sex development.

Authors:  Selma Feldman Witchel
Journal:  Best Pract Res Clin Obstet Gynaecol       Date:  2017-11-22       Impact factor: 5.237

Review 8.  Disorders of sex development (DSD): not only babies with ambiguous genitalia. A practical guide for surgeons.

Authors:  Irene Kearsey; John M Hutson
Journal:  Pediatr Surg Int       Date:  2016-12-18       Impact factor: 1.827

Review 9.  A practical guide for evaluating gonadal germ cell tumor predisposition in differences of sex development.

Authors:  Louise C Pyle; Katherine L Nathanson
Journal:  Am J Med Genet C Semin Med Genet       Date:  2017-05-25       Impact factor: 3.908

Review 10.  Clinical management in mixed gonadal dysgenesis with chromosomal mosaicism: Considerations in newborns and adolescents.

Authors:  Erica M Weidler; Margaret Pearson; Kathleen van Leeuwen; Erin Garvey
Journal:  Semin Pediatr Surg       Date:  2019-09-19       Impact factor: 2.754

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