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Licensed Unlicensed Requires Authentication Published by De Gruyter August 15, 2015

Topical dihydrotestosterone to treat micropenis secondary to partial androgen insensitivity syndrome (PAIS) before, during, and after puberty – a case series

  • David Becker , Lisa M. Wain , Yih Harng Chong , Sonal J. Gosai , Nina K. Henderson , Jacqui Milburn , Victoria Stott and Benjamin J. Wheeler EMAIL logo

Abstract

Background: X-linked partial androgen insensitivity syndrome (PAIS) causes under-virilization at all stages of development. In two thirds of males, this results in micropenis. Dihydrotestosterone (DHT) is a potent androgen that is critical for male genital development, which when applied topically, has been shown to increase penile length with micropenis of varying etiologies. We present the first case series using topical DHT gel to treat micropenis in 46,XY males with PAIS, before, during, and after puberty.

Methods: Three related 46,XY males with confirmed p.L712F androgen receptor mutations exhibited varying degrees of micropenis post-surgical correction. They were of pre-pubertal, peri-pubertal and adult ages, respectively. Following baseline clinical and laboratory assessments all completed a 4-month course of daily DHT gel 2.5% (androstanolone) topically to penis (0.3 mg/kg body weight), with monitoring for adverse effects. Primary outcome was change in stretched penile length (SPL) following treatment.

Results: Mixed results were obtained following topical DHT therapy. In the pre- and peri- pubertal patients, SPL changed from 2.5 cm to 3.5 cm (+40%), and 3.5 cm to 5.7 cm (+63%), respectively. In the adult patient with 1 year of prior high-dose weekly testosterone therapy, no additional change in SPL was seen. No adverse effects of topical DHT were reported or observed throughout the 4 months of treatment.

Conclusions: Topical DHT treatment appears to be a safe and well-tolerated method of virilising micropenis both prior to and during puberty in children with PAIS. Questions remain about long-term outcomes into adulthood, and efficacy in adults with prior lengthy exposure to high-dose testosterone.


Corresponding author: Dr. Benjamin J. Wheeler, Paediatric Endocrinologist, Department of Women’s and Children’s Health, University of Otago, PO Box 913, Dunedin 9054, New Zealand, Phone: 0064 3 4740999, Fax: 0064 3 4747817, E-mail: ; and Paediatric Endocrinology, Southern District Health Board, Dunedin, New Zealand

Acknowledgments

The authors wish to thank the participants and their families for their forbearance and generous participation.

Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

Research funding: None declared.

Employment or leadership: None declared.

Honorarium: None declared.

Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2015-4-24
Accepted: 2015-7-20
Published Online: 2015-8-15
Published in Print: 2016-2-1

©2016 by De Gruyter

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