| Literature DB >> 30679975 |
Irena Nedelea1,2, Diana Deleanu1,2,3.
Abstract
Angioedema can occur in isolation, accompanied by urticaria, or as a feature of anaphylaxis in mast cell-mediated disorders, bradykinin-mediated disorders, as well as in others with unknown mechanisms, such as infections, rare disorders, or idiopathic angioedema. In mast cell-mediated angioedema, other signs and symptoms of mast cell-mediator release are frequently seen. However, clear evidence of mast cell degranulation may be absent in histaminergic angioedema. Bradykinin-induced angioedema is not associated with urticaria or other symptoms of type I hypersensitivity reactions. For many of the known triggers of angioedema, the mechanism is unclear. While mast cell and bradykinin-mediated angioedema are relatively well defined in terms of diagnostic and therapeutic approach, angioedema with unknown mechanisms represents a challenge for patients and clinicians alike. Elucidating the clinical pattern and the possible causes of isolated angioedema is the key to a correct diagnosis. This review summarizes the causes, and clinical features of angioedema, with a focus on isolated angioedema.Entities:
Keywords: acquired angioedema; bradykinin-mediated angioedema; hereditary angioedema; histaminergic angioedema; idiopathic angioedema
Year: 2018 PMID: 30679975 PMCID: PMC6327642 DOI: 10.3892/etm.2018.6982
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447