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Therapeutic Challenges in the Management of VEXAS Syndrome: A Case Report
Georgia Kelly1, Yolanka Lobo2, Amanda Godbolt1
1Royal Brisbane and Women's Hospital, Brisbane, Australia.
Abstract:
VEXAS syndrome is a newly described autoinflammatory and haematologic condition that has variable cutaneous and systemic presentations. We present a case of VEXAS syndrome in a 63-year-old male with treatment refractory pyoderma gangrenosum and a complex dermatologic and systemic history. We hope it informs and encourages dermatologists to consider early diagnostic testing for VEXAS syndrome in any male over 50 years of age with a neutrophilic dermatosis and unexplained autoinflammation.
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