| Literature DB >> 27656513 |
Mustafa Gazi Uçar1, Tolgay Tuyan Ilhan2, Ayse Gül Kebapçilar3, Zekeriya Tosun4, Çetin Çelik5.
Abstract
Urethral coitus is an extremely rare condition. Megalourethra and urinary incontinence due to urethral coitus in vaginal agenesis are unusual manifestations because these patients usually present with primary amenorrhea before becoming sexually active and receive treatment. A 24-year-old woman came to our clinic because of primary amenorrhea, sexual dysfunction, dyspareunia, megalourethra and urinary incontinence five months after her marriage due to urethral coitus. Based on these clinical and radiological findings a diagnosis of Mayer-Rokitansky-Kuster-Hauser Syndrome was made and patient underwent modified McIndoe Vaginoplasty. The elasticity of female urethra permits repeated coitus, together with the physical damage can probably lead to incontinence. In this case, after eliminating the underlying cause of disease with vaginoplasty, no other treatment was required. The integrity of sphincteric function and structural support of urethra might be regained without subjecting the patient to aggressive reconstructive surgical procedures.Entities:
Keywords: Full-thickness skin graft vaginoplasty; Mayer-rokitansky-kuster-hauser syndrome; Megalourethra, Urethral coitus
Year: 2016 PMID: 27656513 PMCID: PMC5028464 DOI: 10.7860/JCDR/2016/20106.8256
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X