Matches in SemOpenAlex for { <https://semopenalex.org/work/W4254197957> ?p ?o ?g. }
Showing items 1 to 74 of
74
with 100 items per page.
- W4254197957 endingPage "182" @default.
- W4254197957 startingPage "182" @default.
- W4254197957 abstract "BackgroundIsolated distal vaginal agenesis is a rare Müllerian duct anomaly and usually presents at or after menarche with a complaint of abdominal pain due to hematometrocolpos. We describe an unusual presentation of this anomaly in a prepubertal girl.CaseA 11-years-old girl with a history of recurrent urinary infection, pyuria and right-sided renal agenesis was referred to our tertiary care center. Gynecologic examination revealed normally developed labia majora and minora with absence of an external vaginal opening (Figure 1). She hadn’t had breast, pubic and axillary hair development. Transrectal ultrasound demonstrated upper vagina and uterus filled with fluid. Opening of dystal vaginal agenesis was planned. Pyocolpos was discharged following dissection of about three centimeters atretic portion. Uterus and vagina were found to be filled with pus. Pull-through vaginoplasty procedure was performed and vaginal mold was placed (Figure 2). After 1 week antibiotherapy and a result of sterile urine culture, cystoscopy was performed for suspicion of congenital vesicouterine fistula but no abnormalities were seen. Postoperative period was uneventful and mold left in place for three months. The authors theorize that pyuria could have resulted from transition of pus from pycolpos through the vagina and bladder wall.CommentsFigure 2Postoperative view of external genitalia of the patient.View Large Image Figure ViewerDownload Hi-res image Download (PPT) BackgroundIsolated distal vaginal agenesis is a rare Müllerian duct anomaly and usually presents at or after menarche with a complaint of abdominal pain due to hematometrocolpos. We describe an unusual presentation of this anomaly in a prepubertal girl. Isolated distal vaginal agenesis is a rare Müllerian duct anomaly and usually presents at or after menarche with a complaint of abdominal pain due to hematometrocolpos. We describe an unusual presentation of this anomaly in a prepubertal girl. CaseA 11-years-old girl with a history of recurrent urinary infection, pyuria and right-sided renal agenesis was referred to our tertiary care center. Gynecologic examination revealed normally developed labia majora and minora with absence of an external vaginal opening (Figure 1). She hadn’t had breast, pubic and axillary hair development. Transrectal ultrasound demonstrated upper vagina and uterus filled with fluid. Opening of dystal vaginal agenesis was planned. Pyocolpos was discharged following dissection of about three centimeters atretic portion. Uterus and vagina were found to be filled with pus. Pull-through vaginoplasty procedure was performed and vaginal mold was placed (Figure 2). After 1 week antibiotherapy and a result of sterile urine culture, cystoscopy was performed for suspicion of congenital vesicouterine fistula but no abnormalities were seen. Postoperative period was uneventful and mold left in place for three months. The authors theorize that pyuria could have resulted from transition of pus from pycolpos through the vagina and bladder wall. A 11-years-old girl with a history of recurrent urinary infection, pyuria and right-sided renal agenesis was referred to our tertiary care center. Gynecologic examination revealed normally developed labia majora and minora with absence of an external vaginal opening (Figure 1). She hadn’t had breast, pubic and axillary hair development. Transrectal ultrasound demonstrated upper vagina and uterus filled with fluid. Opening of dystal vaginal agenesis was planned. Pyocolpos was discharged following dissection of about three centimeters atretic portion. Uterus and vagina were found to be filled with pus. Pull-through vaginoplasty procedure was performed and vaginal mold was placed (Figure 2). After 1 week antibiotherapy and a result of sterile urine culture, cystoscopy was performed for suspicion of congenital vesicouterine fistula but no abnormalities were seen. Postoperative period was uneventful and mold left in place for three months. The authors theorize that pyuria could have resulted from transition of pus from pycolpos through the vagina and bladder wall. Comments" @default.
- W4254197957 created "2022-05-12" @default.
- W4254197957 creator A5000201770 @default.
- W4254197957 creator A5024059301 @default.
- W4254197957 creator A5030187822 @default.
- W4254197957 creator A5037660208 @default.
- W4254197957 creator A5054741023 @default.
- W4254197957 creator A5071128845 @default.
- W4254197957 creator A5090308322 @default.
- W4254197957 date "2016-04-01" @default.
- W4254197957 modified "2023-10-18" @default.
- W4254197957 title "A Case of Distal Vaginal Agenesis Presenting With Recurrent Urinary Tract Infection and Pyuria in a Prepubertal Girl" @default.
- W4254197957 doi "https://doi.org/10.1016/j.jpag.2016.01.058" @default.
- W4254197957 hasPublicationYear "2016" @default.
- W4254197957 type Work @default.
- W4254197957 citedByCount "0" @default.
- W4254197957 crossrefType "journal-article" @default.
- W4254197957 hasAuthorship W4254197957A5000201770 @default.
- W4254197957 hasAuthorship W4254197957A5024059301 @default.
- W4254197957 hasAuthorship W4254197957A5030187822 @default.
- W4254197957 hasAuthorship W4254197957A5037660208 @default.
- W4254197957 hasAuthorship W4254197957A5054741023 @default.
- W4254197957 hasAuthorship W4254197957A5071128845 @default.
- W4254197957 hasAuthorship W4254197957A5090308322 @default.
- W4254197957 hasConcept C105702510 @default.
- W4254197957 hasConcept C126322002 @default.
- W4254197957 hasConcept C141071460 @default.
- W4254197957 hasConcept C2775886723 @default.
- W4254197957 hasConcept C2776316342 @default.
- W4254197957 hasConcept C2776845205 @default.
- W4254197957 hasConcept C2777744392 @default.
- W4254197957 hasConcept C2778619298 @default.
- W4254197957 hasConcept C2778769751 @default.
- W4254197957 hasConcept C2780011137 @default.
- W4254197957 hasConcept C2780091579 @default.
- W4254197957 hasConcept C2780136519 @default.
- W4254197957 hasConcept C2781218831 @default.
- W4254197957 hasConcept C71924100 @default.
- W4254197957 hasConcept C77411442 @default.
- W4254197957 hasConceptScore W4254197957C105702510 @default.
- W4254197957 hasConceptScore W4254197957C126322002 @default.
- W4254197957 hasConceptScore W4254197957C141071460 @default.
- W4254197957 hasConceptScore W4254197957C2775886723 @default.
- W4254197957 hasConceptScore W4254197957C2776316342 @default.
- W4254197957 hasConceptScore W4254197957C2776845205 @default.
- W4254197957 hasConceptScore W4254197957C2777744392 @default.
- W4254197957 hasConceptScore W4254197957C2778619298 @default.
- W4254197957 hasConceptScore W4254197957C2778769751 @default.
- W4254197957 hasConceptScore W4254197957C2780011137 @default.
- W4254197957 hasConceptScore W4254197957C2780091579 @default.
- W4254197957 hasConceptScore W4254197957C2780136519 @default.
- W4254197957 hasConceptScore W4254197957C2781218831 @default.
- W4254197957 hasConceptScore W4254197957C71924100 @default.
- W4254197957 hasConceptScore W4254197957C77411442 @default.
- W4254197957 hasIssue "2" @default.
- W4254197957 hasLocation W42541979571 @default.
- W4254197957 hasOpenAccess W4254197957 @default.
- W4254197957 hasPrimaryLocation W42541979571 @default.
- W4254197957 hasRelatedWork W1510797021 @default.
- W4254197957 hasRelatedWork W2034858744 @default.
- W4254197957 hasRelatedWork W2073673012 @default.
- W4254197957 hasRelatedWork W2124916431 @default.
- W4254197957 hasRelatedWork W2279848799 @default.
- W4254197957 hasRelatedWork W2377078247 @default.
- W4254197957 hasRelatedWork W2378336733 @default.
- W4254197957 hasRelatedWork W2418684978 @default.
- W4254197957 hasRelatedWork W2946607552 @default.
- W4254197957 hasRelatedWork W96547481 @default.
- W4254197957 hasVolume "29" @default.
- W4254197957 isParatext "false" @default.
- W4254197957 isRetracted "false" @default.
- W4254197957 workType "article" @default.