Diagnose und Therapie der Granulomatose mit Polyangiitis und mikroskopische Polyangiitis – 2023: Konsens-Empfehlungen der Österreichischen Gesellschaften für Nephrologie (ÖGN) & Rheumatologie (ÖGR)

ANCA-associated vasculitides (AAV) are rare, complex systemic diseases that are often difficult to diagnose, because of unspecific clinical symptoms at presentation. However, the clinical course may be very dramatic and even life-threatening, necessitating prompt diagnosis and treatment. Therefore,...

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Detalles Bibliográficos
Autores principales: Odler, Balazs, Windpessl, Martin, Eller, Kathrin, Säemann, Marcus D., Lhotta, Karl, Neumann, Irmgard, Öberseder, Gregor, Duftner, Christina, Dejaco, Christian, Rudnicki, Michael, Gauckler, Philipp, Hintenberger, Rainer, Zwerina, Jochen, Thiel, Jens, Kronbichler, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2023
Materias:
Konsensus-Empfehlungen
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511611/
https://www.ncbi.nlm.nih.gov/pubmed/37728651
http://dx.doi.org/10.1007/s00508-023-02262-9
Descripción
Sumario:ANCA-associated vasculitides (AAV) are rare, complex systemic diseases that are often difficult to diagnose, because of unspecific clinical symptoms at presentation. However, the clinical course may be very dramatic and even life-threatening, necessitating prompt diagnosis and treatment. Therefore, it is important to increase disease awareness among physicians and support colleagues who are not confronted with these rare diseases on a regular basis. Here, the Austrian Society of Nephrology (ÖGN) and the Austrian Society of Rheumatology (ÖGR) provide a joint consensus on how to best diagnose and manage patients with granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA).

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