OHVIRA syndrome: A case report treated with delayed diagnosis and multidisciplinary approaches

OHVIRA syndrome is a rare condition involving genitourinary anomalies, where early diagnosis and intervention can reduce the need for complex treatment processes and surgical interventions.

A 42-year-old female patient was diagnosed with OHVIRA syndrome and treated with antibiotic therapy and vaginal septectomy; however, due to elevated CRP levels and severe abdominal pain, a hysterectomy was performed. Post-surgery, the patient showed improvement and was discharged.

OHVIRA syndrome is a rare congenital anomaly that manifests with symptoms during adolescence. The diagnostic and treatment process can be challenging and may involve various complications. Early diagnosis and minimally invasive surgery alleviate symptoms and preserve reproductive potential. This case report highlights the multidisciplinary management of OHVIRA syndrome and the complexities of the treatment processes.