| Autor: |
Moshiri M, Seyal AR, Cruite I, Bhargava P |
| Jazyk: |
angličtina |
| Zdroj: |
Radiology case reports [Radiol Case Rep] 2015 Dec 07; Vol. 7 (4), pp. 800. Date of Electronic Publication: 2015 Dec 07 (Print Publication: 2012). |
| DOI: |
10.2484/rcr.v7i4.800 |
| Abstrakt: |
Uterine didelphys with obstructed hemivagina and ipsilateral renal agenesis is a rare congenital anomaly of the Müllerian duct system referred to as Herlyn-Werner-Wunderlich syndrome. Because of its rare occurrence, a high level of suspicion is often required for diagnosis. Clinically, these patients usually present after menarche with pelvic pain, dysmenorrhea, and a palpable pelvic mass. We present a case of a 31-year-old female patient with infertility. Imaging findings were consistent with Herlyn-Werner-Wunderlich syndrome, with a congenital defect in the longitudinal vaginal septum resulting in partial spontaneous decompression of right-sided hematocolpos. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
|
