Evidence map›Paper›PMID 42416455›Full record

ArticleInternational journal of surgery case reports2026

Experience with isolated female epispadias repair: case report from Northern Tanzania.

Donald Dominick Lema, Bartholomeo Nicholaus Ngowi, Deodatha Leonard Rubagumya, Mshangama Juma Seif, Jacques Bogdanowicz, Orgeness Jasper Mbwambo

Abstract readCase Reports
In one paragraph

Article in International journal of surgery case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Donald Dominick LemaFaculty of Medicine, KCMC University, Moshi, Tanzania.ORCID https://orcid.org/0009-0004-7324-1259
Bartholomeo Nicholaus NgowiFaculty of Medicine, KCMC University, Moshi, Tanzania.ORCID https://orcid.org/0000-0002-1898-9772
Deodatha Leonard RubagumyaFaculty of Medicine, KCMC University, Moshi, Tanzania.ORCID https://orcid.org/0009-0003-4983-6247
Mshangama Juma SeifFaculty of Medicine, KCMC University, Moshi, Tanzania.ORCID https://orcid.org/0009-0003-7464-6963
Jacques BogdanowiczFaculty of Medicine, KCMC University, Moshi, Tanzania.ORCID https://orcid.org/0009-0009-0828-0565
Orgeness Jasper MbwamboFaculty of Medicine, KCMC University, Moshi, Tanzania.ORCID https://orcid.org/0000-0001-6689-3452

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Female epispadias is a rare congenital anomaly resulting from disrupted mesodermal migration during embryogenesis, leading to anterior urethral displacement, a wide bladder neck, and a bifid clitoris without bladder exstrophy. Diagnosis is clinical, and defects are classified according to the degree of meatal displacement. Case presentation: The first case involved a 5-month-old infant with a congenital abnormal urethral opening, dorsal urethral cleft, cephalad-displaced meatus, and a bifid clitoris, with normal imaging. She underwent urethroplasty without bladder neck reconstruction and recovered uneventfully. The second case was a 4-year-old girl presenting with an abnormal urethral opening and lifelong urinary incontinence. Examination revealed a dorsal urethral cleft, cephalad-displaced meatus, and a bifid clitoris, with no visible bladder mucosa. She underwent perineal urethrocervicoplasty and achieved continence. Both patients demonstrated good bladder capacity, minimal residual urine, preserved renal function, and satisfactory cosmetic outcomes at 3-6 months of follow-up. Clinical discussion: Most girls with isolated epispadias are incontinent and require individualized urethral and bladder neck reconstruction tailored to age and defect severity. Surgical approaches vary, but single-stage perineal urethrocervicoplasty may offer favorable cosmetic outcomes and improved continence compared with traditional techniques such as the Young-Dees procedure. Conclusion: Early recognition and tailored surgical reconstruction are essential for isolated female epispadias. Age-appropriate staged or single-stage repairs can achieve continence, preserve upper urinary tract function, improve cosmetic appearance, and enhance quality of life. Long-term follow-up is recommended.

Indexed as

case reportepispadias repairfemale epispadiasisolated epispadiasperineal urethrocervicoplasty

Identifiers

PMID42416455
PMCPMC13340707

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.