"Idiopathic eosinophilic vasculitis": another side of hypereosinophilic syndrome? A comprehensive analysis of 117 cases in asthma-free patients.

Date publication

décembre 2019

Journal

The journal of allergy and clinical immunology. In practice

Auteurs

Membres identifiés du Cancéropôle Est :
Pr MARTIN Thierry

Tous les auteurs :
Lefèvre G, Leurs A, Gibier JB, Copin MC, Staumont-Sallé D, Dezoteux F, Chenivesse C, Lopez B, Terriou L, Hachulla E, Launay D, Etienne N, Labalette M, DeGroote P, Pontana F, Quemeneur T, Hatron PY, Schleinitz N, Viallard JF, Hamidou M, Martin T, Morati-Hafsaoui C, Groh M, Lambert M, Kahn JE,

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/31863912

Résumé

The absence of asthma may rule out a diagnosis of eosinophilic granulomatosis with polyangiitis (EGPA) in patients with hypereosinophilic syndrome (HES) and features of vasculitis.

Mots clés

eosinophilic disorder, eosinophilic granulomatosis with polyangiitis, eosinophilic vasculitis, hypereosinophilic syndrome

Référence

J Allergy Clin Immunol Pract. 2019 Dec 18;: