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Complications aiguës des vascularites associées aux ANCA

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Maladies rares en médecine d’urgence

Part of the book series: Références en médecine d’urgence. Collection de la SFMU ((REFERMED))

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Résumé

Les vascularites associées aux anticorps anti-cytoplasme (ANCA) de polynucléaires neutrophiles (AAV) sont des vascularites intéressant de façon prédominante les vaisseaux de petits calibres et comprennent la granulomatose avec polyangéite (GPA), anciennement dénommée granulomatose de Wegener, la polyangéite microscopique (PAM) et le syndrome de Churg et Strauss (SCS) dont le nom sera très prochainement modifié pour « granulomatose éosinophilique avec polyangéite ». Les dates clés dans l’histoire des AAV sont: la première description de la GPA par Friedrich Wegener en 1936, la première description de la PAM en 1948 et la description des ANCA en 1982.

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Authors and Affiliations

  1. Service de médecine interne, Institut Mutualiste Montsouris, 42, Boulevard Jourdan, 75014, Paris, France

    P. Charles

  2. Service de médecine interne, Centre de Référence pour les maladies auto-immunes rares (vascularites nécrosantes sclérodermie systémique), Hôpital Cochin, AP-HP, 27, rue du Faubourg Saint-Jacques, 75014, Paris, France

    X. Puéchal

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Charles, P., Puéchal, X. (2013). Complications aiguës des vascularites associées aux ANCA. In: Maladies rares en médecine d’urgence. Références en médecine d’urgence. Collection de la SFMU. Springer, Paris. https://doi.org/10.1007/978-2-8178-0350-0_9

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  • DOI: https://doi.org/10.1007/978-2-8178-0350-0_9

  • Publisher Name: Springer, Paris

  • Print ISBN: 978-2-8178-0349-4

  • Online ISBN: 978-2-8178-0350-0

  • eBook Packages: MedicineMedicine (R0)

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