Gonadal Function in Boys with Bilateral Undescended Testes

Author:

Lucas-Herald Angela K1ORCID,Alkanhal Khalid I12,Caney Emma1,Malik Iman1,Alimussina Malika1,McNeilly Jane D3,Bradnock Timothy4,Lee Boma5,Steven Mairi5,Flett Martyn5ORCID,O’Toole Stuart5,McGowan Ruth16,Faisal Ahmed S1ORCID

Affiliation:

1. Developmental Endocrinology Research Group, University of Glasgow, Royal Hospital for Children , Glasgow G51 4TF , UK

2. Obesity and Endocrine Metabolism Center, King Fahad Medical City , 58046 Riyady 11525 , Saudi Arabia

3. Department of Clinical Biochemistry, Queen Elizabeth University Hospital , Glasgow G51 4TF , UK

4. Department of General Paediatric Surgery, Royal Hospital for Children , Glasgow G51 4TF , UK

5. Department of Paediatric Urology, Royal Hospital for Children , Glasgow G51 4TF , UK

6. West of Scotland Centre for Genomic Medicine, Queen Elizabeth University Hospital , Glasgow G51 4TF , UK

Abstract

Abstract Background Bilateral undescended testes (BUDT) may be a marker of an underlying condition that affects sex development or maturation. Aims To describe the extent of gonadal dysfunction in cases of BUDT who had systematic endocrine and genetic evaluation at a single tertiary pediatric center. Methods A retrospective review was conducted of all boys with BUDT who had endocrine evaluation between 2008 and 2021 at the Royal Hospital for Children, Glasgow (RHCG). Continuous variables were analyzed using Mann–Whitney U and non-continuous variables using Fisher’s exact, via Graphpad Prism v 8.0. Multivariable logistic regression was used to identify any associations between groups. A P < .05 was considered statistically significant. Results A total of 243 bilateral orchidopexies were performed at RHCG between 2008 and 2021. Of these 130 (53%) boys were seen by the endocrine team. The median (range) age at first orchidopexy was 1 year (0.2, 18.0) with 16 (12%) requiring re-do orchidopexy. The median External Masculinization Score of the group was 10 (2, 11) with 33 (25%) having additional genital features. Of the 130 boys, 71 (55%) had extragenital anomalies. Of the 70 who were tested, a genetic abnormality was detected in 38 (54%), most commonly a chromosomal variant in 16 (40%). Of the 100 who were tested, endocrine dysfunction was identified in 38 (38%). Conclusion Genetic findings and evidence of gonadal dysfunction are common in boys who are investigated secondary to presentation with BUDT. Endocrine and genetic evaluation should be part of routine clinical management of all cases of BUDT.

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

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