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Successful Treatment of Severe Purpura Fulminans With Anakinra
Francesco Zulian1, Luca Spiezia2, Antonio Amabile3
1Department of Women's and Children's Health, Padova University Hospital, Padova, Italy.
Abstract:
Purpura fulminans (PF) is a rare, often fatal pediatric condition characterized by intravascular thrombosis and hemorrhagic infarction of the skin. A timely diagnosis and treatment are paramount to prevent the involvement of internal organs, causing disseminated intravascular coagulation and gangrene of the extremities. The management of PF requires a comprehensive approach, including the treatment of the underlying infection, anticoagulation, and anti-inflammatory therapy. Herein we present the case of a child with severe PF successfully treated with anakinra, an anti-IL1-receptor monoclonal antibody.
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