Bonadonna Patrizia, Bonifacio Massimiliano, Lombardo Carla, Zanotti Roberta
Allergy Unit, Azienda Ospedaliera Universitaria Integrata di Verona, Piazzale Stefani 1, 37126, Verona, Italy.
Multidisciplinary Outpatients clinics for Mastocytosis (GISM), Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Curr Allergy Asthma Rep. 2016 Jan;16(1):5. doi: 10.1007/s11882-015-0582-5.
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.
肥大细胞活化综合征(MCAS)可在具有源自肥大细胞(MC)的介质引起的反复严重症状的患者中诊断出来,这些介质在血清中短暂升高,并可被靶向介质的药物所减轻。当在这些患者中检测到KIT突变的克隆性MC时,可作出原发性MCAS的诊断。对膜翅目毒液(HV)的严重全身反应是肥大细胞增多症患者中最常见的过敏反应形式。原发性MCAS和HV过敏反应的患者主要为男性,大多数病例没有皮肤病变,过敏反应的特征是在没有荨麻疹和血管性水肿的情况下出现低血压和晕厥。这些患者中正常的类胰蛋白酶值(≤11.4 ng/ml)并不能排除肥大细胞增多症的诊断。原发性MCAS和HV过敏反应的患者必须接受终身毒液免疫治疗,以预防进一步可能致命的严重反应。