Incidental diagnosis of Herlyn-Werner-Wunderlich Syndrome in a nulliparous woman: a case report in Bhutan
This case report describes the incidental diagnosis of Herlyn-Werner-Wunderlich syndrome in a 42-year-old nulliparous woman presenting with abdominal pain, which was confirmed by imaging and treated for associated endometriosis.
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This case report describes the incidental diagnosis of Herlyn-Werner-Wunderlich syndrome, a rare congenital condition characterized by uterus didelphys, an ipsilateral absent kidney, and an obstructed hemivagina, in a 42-year-old nulliparous woman presenting with right-sided abdominal pain in Bhutan. The authors used ultrasound, CT, and MRI to support the diagnosis. The report states that the patient was treated for endometriosis and had symptomatic improvement, while noting that delayed or challenging diagnosis can lead to complications such as endometriosis, infertility, and pelvic inflammation. Relevance to endometriosis: the paper explicitly links late diagnosis of Herlyn-Werner-Wunderlich syndrome to endometriosis and reports that the patient received endometriosis treatment with symptom improvement, though the paper is primarily a HWWS case report.
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References (17)
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