UTERUS DIDELFIS, OBSTRÜKTE HEMIVAJEN VE İPSILATERAL RENAL AGENEZI: OHRIVA SENDROMU
| Autor: | Kurt, Raziye, Atci, Nesrin, Karapınar, Oya, Kokoçya, Sümeyye, Hakverdi, Ali, Okyay, Ayşe |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2015 |
| Předmět: |
lcsh:R5-920
congenital hereditary and neonatal diseases and abnormalities obstructed hemivagina lcsh:R lcsh:Medicine nutritional and metabolic diseases obsrükte hemivajen uterus didelphys mullerian anomaly mülleryan anomali obsrükte hemivajen OHRIVA sendromu uterus didelfis mülleryan anomali obsrükte hemivajen OHRIVA sendromu uterus didelfis Health Care Sciences and Services mülleryan anomali uterus didelfis mullerian anomaly obstructed hemivagina OHRIVA syndrome uterus didelphys Sağlık Bilimleri ve Hizmetleri lcsh:Medicine (General) mullerian anomaly obstructed hemivagina OHRIVA syndrome uterus didelphys OHRIVA syndrome OHRIVA sendromu |
| Zdroj: | Volume: 4, Issue: 16 44-46 The Medical Journal of Mustafa Kemal University Mustafa Kemal Üniversitesi Tıp Dergisi, Vol 4, Iss 16, Pp 44-46 (2015) |
| ISSN: | 2149-3103 |
| Popis: | 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. 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 |
| Databáze: | OpenAIRE |
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