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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Cicardi, M; Aberer, W; Banerji, A; Bas, M; Bernstein, JA; Bork, K; Caballero, T; Farkas, H; Grumach, A; Kaplan, AP; Riedl, MA; Triggiani, M; Zanichelli, A; Zuraw, B; HAWK under the patronage of EAACI (European Academy of Allergy and Clinical Immunology).
Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group.
Allergy. 2014; 69(5):602-616 Doi: 10.1111/all.12380 [OPEN ACCESS]
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Co-Autor*innen der Med Uni Graz
Aberer Werner
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Abstract:
Angioedema is defined as localized and self-limiting edema of the subcutaneous and submucosal tissue, due to a temporary increase in vascular permeability caused by the release of vasoactive mediator(s). When angioedema recurs without significant wheals, the patient should be diagnosed to have angioedema as a distinct disease. In the absence of accepted classification, different types of angioedema are not uniquely identified. For this reason, the European Academy of Allergy and Clinical Immunology gave its patronage to a consensus conference aimed at classifying angioedema. Four types of acquired and three types of hereditary angioedema were identified as separate forms from the analysis of the literature and were presented in detail at the meeting. Here, we summarize the analysis of the data and the resulting classification of angioedema. © 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Find related publications in this database (using NLM MeSH Indexing)
Angioedema - diagnosis
Angioedema - drug therapy
Angioedema - etiology
Humans -

Find related publications in this database (Keywords)
urticaria
dermatology
education
clinical immunology
angioedema
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