45 years' experience with early childhood anatomical technique of feminising genitoplasty for 46 XX Congenital Adrenal Hyperplasia -observations of vaginal introital anatomy and its relationship to the perineal body.

Bulbo spongiosus muscle Clitoral reduction Congenital Adrenal Hyperplasia Disorder of sexual differentiation Feminising genitoplasty Perineal body Spongiosum Vaginal Introitus Vaginoplasty Vulvoplasty

Journal

Journal of pediatric urology
ISSN: 1873-4898
Titre abrégé: J Pediatr Urol
Pays: England
ID NLM: 101233150

Informations de publication

Date de publication:
Oct 2022
Historique:
received: 26 11 2021
revised: 26 05 2022
accepted: 10 07 2022
pubmed: 16 8 2022
medline: 15 12 2022
entrez: 15 8 2022
Statut: ppublish

Résumé

In Manchester, feminising genitoplasty is offered to children with 46XX Congenital Adrenal Hyperplasia (CAH) when there is a single perineal opening and/or enlarged clitoris. Our aims are to describe the anatomical reconstructive technique and present long-term outcomes. Our hypothesis is that 'the common channel (CC) length and distance to the vagina from perineal skin is mostly due to virilisation and hypertrophy of perineal tissue over the almost normally positioned vaginal introitus (V-I) in relation to the perineal body (PB)'. METHOD AND RESULTS: This is a retrospective notes review of all consecutive 46XX CAH operations from 1976 to December 2021. 99 patients, who had feminising genitoplasty and being followed-up, were included. 15 patients who were lost to follow up were excluded. Median age at surgery was 15 months. In 91, midline division of the labia majora, spongiosum, bulbo-spongiosus muscle (BSM) and CC down to PB was performed. This was sufficient to expose the V-I at the same level or within 5 mm depth of PB in 88. In 78 V-I was adequate taking 10/12fr dilator (Type 1). In 10, CC resembled a male urethra and V-I was narrow (Type 2), requiring widening by 5-10 mm incision at 6 o'clock position. Dartos of labia majora was attached to BSM to reduce the distance to V-I from perineal skin and the gap was lined with inner foreskin to create a vestibule. Out of 70 who were post-pubertal, 75% (53/70) had adequate calibre vaginal openings. 5 had introitoplasty and 2 had dilatation under anaesthesia. 10 needed self dilators only. 29 patients, of one of the three surgeons, had measurements of clitoris, CC, urethra and vagina. A hymen was found in 86% (25/29). There was significant strong, inverse correlation between the CC length and the urethral length (r = -0.708, p < 0.001, n = 27) but not between CC and vaginal lengths. After adjusting for age, the urethral length of Type 2 patients was 3.825 mm shorter than those of Type 1 (p = 0.017). CONCLUSION: Our data show that 'high' confluence is mostly due to virilisation of genitalia; and the anatomical technique of reversing the fusion of the urethral folds, spongiosum and bulbo-spongiosus muscle could be performed with all degrees of virilisation with success in early childhood with no need of local flaps or mobilisation of the urethro-vaginal complex. About 10% require surgery to treat narrowing of vaginal opening post puberty.

Identifiants

pubmed: 35970739
pii: S1477-5131(22)00309-6
doi: 10.1016/j.jpurol.2022.07.007
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

611.e1-611.e8

Informations de copyright

Copyright © 2022 Journal of Pediatric Urology Company. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest There is no conflict of interest.

Auteurs

Supul Hennayake (S)

Paediatric Urology Department, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, United Kingdom. Electronic address: Supul.Hennayake@mft.nhs.uk.

Abigail Barnes (A)

University of Manchester School of Medicine, The University of Manchester Faculty of Biology Medicine and Health, The University of Manchester, Oxford Road, Manchester, M13 9PL, United Kingdom.

Arianna Mariotto (A)

Paediatric Urology Department, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, United Kingdom.

Anju Goyal (A)

Paediatric Urology Department, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, United Kingdom.

Akinlabi Ajao (A)

Paediatric Urology Department, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, United Kingdom.

Tamas Cserni (T)

Paediatric Urology Department, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, United Kingdom.

Gail Busby (G)

Paediatric and Adolescent Gynaecology, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, United Kingdom.

Leena Patel (L)

Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, United Kingdom; Division of Medical Education, University of Manchester, Oxford Road, Manchester, M13 9PL, United Kingdom.

Mars Skae (M)

Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, United Kingdom.

Jacqueline Nicholson (J)

Paediatric Clinical Psychology, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, United Kingdom.

Adrian Bianchi (A)

Paediatric Urology Department, Royal Manchester Children's Hospital, Oxford Road, Manchester, M13 9WL, United Kingdom.

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