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A challenging case of Behçet's disease with late diagnosis in a 49-year-old female
International Journal of Orthopaedics and Rheumatology · 2024 · Vol. 6(1) · pp. 33–35
Paul Kaldas✉Miis Akel(Nova Southeastern University)Bharat Maddukuri(Nova Southeastern University)Sahil Shah(Lake Erie College of Osteopathic Medicine)Sergio Hernandez-Borges(Lake Erie College of Osteopathic Medicine)
Abstract
Behçet’s Disease (BD) is a rare, chronic, multi-system vasculitis with a complex and variable clinical presentation, making early diagnosis difficult. We report a case of a 49-year-old female of Middle Eastern descent with a history of recurrent oral ulcers, arthralgias, and erythema nodosum, ultimately diagnosed with BD after years of misdiagnosis. The patient’s response to biologic therapy, specifically Etanercept, highlights the importance of individualized treatment. This case report addresses the diagnostic challenges of BD and emphasizes the importance of early recognition and a multidisciplinary approach to treatment.
Ocular Diseases and Behçet’s SyndromeIgG4-Related and Inflammatory DiseasesRetinal and Optic ConditionsBehcet's diseaseMedicineDiseaseSurgeryPediatricsInternal medicine
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