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Published on: June 2, 2015
Behcet Disease Initially Presenting as Deep Venous Thrombosis: A Case Report
Arun Gurunathan1, David T Teachey, Kudakwashe R Chikwava
1*Division of Oncology Departments of †Pediatrics §Pathology and Laboratory Medicine ¶Division of Hematology, The Children's Hospital of Philadelphia Departments of ‡Pediatrics ∥Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
Abstract:
Behcet disease is a potentially life-threatening multisystemic vasculitis with thrombotic tendency. Mucocutaneous ulcers, arthritis, and uveitis are the most recognizable features, but may be absent at the time of medical evaluation. We report a case in which a 8-year old patient presented with spontaneous bilateral lower extremity deep venous thromboses, and screening for rheumatologic symptoms led to diagnosing Behcet. This case demonstrates that deep venous thromboses can be the initial event bringing a patient with Behcet to medical attention, highlighting the importance of screening for underlying rheumatologic diseases in pediatric patients who present with unprovoked thrombosis.
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