Kawasaki disease in adults: Observations in France and literature review.

Date publication

mars 2016

Journal

Autoimmunity reviews

Auteurs

Membres identifiés du Cancéropôle Est :
Pr HUMBERT Philippe

Tous les auteurs :
Fraison JB, Sève P, Dauphin C, Mahr A, Gomard-Mennesson E, Varron L, Pugnet G, Landron C, Roblot P, Oziol E, Chalhoub G, Galempoix JM, Humbert S, Humbert P, Sbidian E, Grange F, Bayrou O, Cathebras P, Morlat P, Epaulard O, Pavese P, Huong du LT, Zoulim A, Stankovic K, Bachelez H, Smail A, Bachmeyer C, Granel B, Serratrice J, Brinchault G, Mekinian A, Costedoat-Chalumeau N, Bourgarit-Durand A, Puéchal X, Guillevin L, Piram M, Koné-Paut I, Fain O,

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/26631821

Résumé

Kawasaki disease (KD) is a vasculitis that mostly occurs in young children and rarely in adults. We analyzed the characteristics of adult-onset KD (AKD) in France.

Mots clés

Adult, Aspirin, therapeutic use, Cardiovascular Diseases, etiology, France, Humans, Immunoglobulins, Intravenous, therapeutic use, Mucocutaneous Lymph Node Syndrome, complications, United States

Référence

Autoimmun Rev. 2016 Mar;15(3):242-9