Literature DB >> 23639712

Aspirin-exacerbated cutaneous disease.

Mario Sánchez-Borges1, Fernan Caballero-Fonseca, Arnaldo Capriles-Hulett.   

Abstract

It has been recognized that a high proportion of chronic urticaria patients experience symptom aggravation when exposed to aspirin and NSAIDs. This clinical picture is known as Aspirin-exacerbated cutaneous disease. The pathogenesis of these exacerbations is related to the inhibition of cyclooxygenase-1 leading to a decreased synthesis of PGE2 and an increased cysteinyl leukotriene production in the skin and subcutaneous tissues. Patient management comprises the treatment of the underlying cutaneous disease with nonsedating antihistamines and other medications, avoidance of COX-1 inhibitors, and the use of alternative NSAIDs that do not inhibit COX-1 for the relief of pain, inflammation and fever.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 23639712     DOI: 10.1016/j.iac.2012.10.004

Source DB:  PubMed          Journal:  Immunol Allergy Clin North Am        ISSN: 0889-8561            Impact factor:   3.479


  1 in total

1.  The SNP rs3128965 of HLA-DPB1 as a genetic marker of the AERD phenotype.

Authors:  Seung-Hyun Kim; Bo-Young Cho; Hyunna Choi; Eun-Soon Shin; Young-Min Ye; Jong-Eun Lee; Hae-Sim Park
Journal:  PLoS One       Date:  2014-12-23       Impact factor: 3.240

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.