AI Summary & Key Takeaways
AI Insightİn this case report, we aim to present a patient having complaint of dysmenorrhea and diagnosis of Herlyn- Werner Wunderlich Syndrome, characterized by uterus didelphys, obstructed hemivagina and ipsilateral renal agenesis.
📌 3 Key Takeaways
Abstract
Herlyn-Werner-Wunderlich syndrome is a rare urogenital anomaly characterized by uterus didelphys, obstructed hemivagina and ipsilateral renal agenesis. Patients with this syndrome frequently complain about dysmenorrhea, cyclic abdominal pain, acute abdomen and abdominal mass soon after menarche. İn this case report, we aimed to report a thirteen-year old girl who had Herlyn- Werner Wunderlich Syndrome.Uterus didelphys together with obstructed hemivagina is seen rarely. Although patients with uterus didelphys and obstructed hemivagina are usually asymptomatic until menarche, dysmenorrhea becomes the major complaint after menarche. İn this case report, we aim to present a patient having complaint of dysmenorrhea and diagnosis of Herlyn- Werner Wunderlich Syndrome, characterized by uterus didelphys, obstructed hemivagina and ipsilateral renal agenesis.
Özet
Herlyn-Werner-Wunderlich Sendromu uterus didelfis, obstrükte hemivajen ve ipsilateral renal agenezi ile karakterize nadir görülen bir anomalidir. Bu sendroma sahip hastalar sıklıkla menarştan kısa süre sonra başlayan dismenore, siklik abdominal ağrı, akut abdomen ve abdominal kitleden yakınırlar. Bu olgu sunumunda 13 yaşında Herlyn- Werner Wunderlich Sendromlu bir vaka sunmayı amaçladık.Herlyn-Werner-Wunderlich Sendromu uterus didelfis, obstrükte hemivajen ve ipsilateral renal agenezi ile karakterize nadir görülen bir anomalidir. Bu sendroma sahip hastalar sıklıkla menarştan kısa süre sonra başlayan dismenore, siklik abdominal ağrı, akut abdomen ve abdominal kitleden yakınırlar. Bu olgu sunumunda 13 yaşında Herlyn- Werner Wunderlich Sendromlu bir vaka sunmayı amaçladık