Del Principe Domenico, Pietraforte Donatella, Gambardella Lucrezia, Marchesi Alessandra, Tarissi de Jacobis Isabella, Villani Alberto, Malorni Walter, Straface Elisabetta
Department of Therapeutic Research and Medicine Evaluation, Section of Cell Aging and Gender Medicine, Istituto Superiore di Sanità, Rome, Italy.
Department of Neurosciences, Section of Cell Aging and Gender Medicine, Istituto Superiore di Sanità, Rome, Italy.
J Cell Mol Med. 2017 Apr;21(4):632-639. doi: 10.1111/jcmm.12992. Epub 2017 Jan 7.
Kawasaki disease is a multisystemic vasculitis that can result in coronary artery lesions. It predominantly affects young children and is characterized by prolonged fever, diffuse mucosal inflammation, indurative oedema of the hands and feet, a polymorphous skin rash and non-suppurative lymphadenopathy. Coronary artery involvement is the most important complication of Kawasaki disease and may cause significant coronary stenosis resulting in ischemic heart disease. The introduction of intravenous immunoglobulin decreases the incidence of coronary artery lesions to less than 5%. The etiopathogenesis of this disease remains unclear. Several lines of evidence suggest that an interplay between a microbial infection and a genetic predisposition could take place in the development of the disease. In this review, we summarize the state of the art of pathogenetic mechanisms of Kawasaki disease underscoring the relevance of haematological features as a novel field of investigation.
川崎病是一种可导致冠状动脉病变的多系统血管炎。它主要影响幼儿,其特征为持续发热、弥漫性黏膜炎症、手足硬性水肿、多形性皮疹和非化脓性淋巴结病。冠状动脉受累是川崎病最重要的并发症,可能导致严重的冠状动脉狭窄,进而引发缺血性心脏病。静脉注射免疫球蛋白的应用使冠状动脉病变的发生率降至5%以下。该疾病的发病机制仍不清楚。有几条证据表明,微生物感染与遗传易感性之间的相互作用可能在疾病发展过程中发生。在这篇综述中,我们总结了川崎病发病机制的最新研究状况,强调血液学特征作为一个新的研究领域的相关性。