A Successful Single-Stage Reconstruction of an Isolated Female Epispadias in a 14-Year-Old Patient: A Case Report and Literature Review

Epispadias is a rare congenital disorder characterized by an abnormal dorsal opening of the urethra due to the failure of the urethral plate to tubularize. It is usually part of broader conditions like bladder or cloacal exstrophy and rarely occurs in isolation. We present the case of a 14-year-old girl with isolated epispadias who had lifelong urinary incontinence without urgency. Genital examination revealed a bifid clitoris, underdeveloped labia minora, and a widely open urethral meatus with continuous leakage of urine. Urethrocystoscopy showed a short, patulous urethra, a poorly coapting external sphincter, and an open bladder neck. She underwent a successful single-stage surgical repair consisting of urethroplasty, bladder neck reconstruction, and perineoplasty. Two weeks after surgery, following catheter removal, the patient achieved urinary continence. This case supports the effectiveness of single-stage reconstruction even in delayed presentations of isolated female epispadias.

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Publication Details

Journal
International Medical Case Reports Journal
Published
2026-01-01
DOI
https://doi.org/10.2147/imcrj.s559971
Primary Topic
Urological Disorders and Treatments
Type
article
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article

A Successful Single-Stage Reconstruction of an Isolated Female Epispadias in a 14-Year-Old Patient: A Case Report and Literature Review

OV Nyongole, Charles A. Mkony, John Mugisha Kashaija, Naomi Herbert Mtafu et al.
International Medical Case Reports Journal
Urological Disorders and Treatments
article

A Successful Single-Stage Reconstruction of an Isolated Female Epispadias in a 14-Year-Old Patient: A Case Report and Literature Review

OV Nyongole, Charles A. Mkony, John Mugisha Kashaija, Naomi Herbert Mtafu, Joachim Kulwa Mhaya, Ibrahim Ndola, Gabriel Mtaturu, Alexandre Mitamo
article en

Abstract

Epispadias is a rare congenital disorder characterized by an abnormal dorsal opening of the urethra due to the failure of the urethral plate to tubularize. It is usually part of broader conditions like bladder or cloacal exstrophy and rarely occurs in isolation. We present the case of a 14-year-old girl with isolated epispadias who had lifelong urinary incontinence without urgency. Genital examination revealed a bifid clitoris, underdeveloped labia minora, and a widely open urethral meatus with continuous leakage of urine. Urethrocystoscopy showed a short, patulous urethra, a poorly coapting external sphincter, and an open bladder neck. She underwent a successful single-stage surgical repair consisting of urethroplasty, bladder neck reconstruction, and perineoplasty. Two weeks after surgery, following catheter removal, the patient achieved urinary continence. This case supports the effectiveness of single-stage reconstruction even in delayed presentations of isolated female epispadias.

International Medical Case Reports JournalVol. Volume 19
Muhimbili University of Health and Allied Sciences (TZ), Université Catholique du Graben (CD), Muhimbili National Hospital (TZ)
Gender equality
Openalex Percentile: Top 94%
Urological Disorders and Treatments
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