| Literature DB >> 26714690 |
Patrizia Bonadonna1,2, Massimiliano Bonifacio3,4, Carla Lombardo5,6, Roberta Zanotti7,8.
Abstract
Mast cell activation syndrome (MCAS) can be diagnosed in patients with recurrent, severe symptoms from mast cell (MC)-derived mediators, which are transiently increased in serum and are attenuated by mediator-targeting drugs. When KIT-mutated, clonal MC are detected in these patients, a diagnosis of primary MCAS can be made. Severe systemic reactions to hymenoptera venom (HV) represent the most common form of anaphylaxis in patients with mastocytosis. Patients with primary MCAS and HV anaphylaxis are predominantly males and do not have skin lesions in the majority of cases, and anaphylaxis is characterized by hypotension and syncope in the absence of urticaria and angioedema. A normal value of tryptase (≤11.4 ng/ml) in these patients does not exclude a diagnosis of mastocytosis. Patients with primary MCAS and HV anaphylaxis have to undergo lifelong venom immunotherapy, in order to prevent further potentially fatal severe reactions.Entities:
Keywords: Anaphylaxis; Clonal mast cell activation syndromes; Hymenoptera venom allergy; Mast cell activation syndromes; Systemic mastocytosis; Tryptase
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Year: 2016 PMID: 26714690 DOI: 10.1007/s11882-015-0582-5
Source DB: PubMed Journal: Curr Allergy Asthma Rep ISSN: 1529-7322 Impact factor: 4.806