Abstract
IntroductionUrethral coitus is very rare with significant consequences and less than 30 cases were reported in the literature. It is most commonly associated with Mullerian anomalies. ObservationWe report a case of 28 years married woman with Mullerian agenesis and associated anomalies who was engaged in urethral coitus and urethral dilation was detected on examination under anesthesia. The patient did not accept vaginoplasty after she learned that it would not be a cure for her infertility problem. ConclusionsUrethral coitus is very rare with few cases reported. Woman diagnosed with MRKHS II should be assessed for associated abnormalities especially skeletal and renal ones. Urinary incontinence associated with coitus and dyspareunia with Mullerian anomalies should raise the suspicion of urethral coitus. Follow-up is important to avoid urinary tract infections if the female rejects surgery and is satisfied with intra-urethral coitus. Mullerian anomaly should be corrected to allow vaginal intercourse if possible.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.