Thangathurai Jenica, Kalashnikova Mariya, Takahashi Masato, Shinbane Jerold S
Department of Medicine, Division of Cardiology, Harbor-University of California, Los Angeles Medical Center, 1124 W Carson St, RB-2 3rd Floor, Torrance, CA 90502 (J.T.); Department of Medicine, Brigham and Women's Hospital and Harvard School of Medicine, Boston, Mass (M.K.); Department of Pediatrics, University of Washington School of Medicine and Heart Center, Seattle Children's Hospital, Seattle, Wash (M.T.); and Division of Cardiovascular Medicine, Keck School of Medicine of the University of Southern California, Health Science Campus, Los Angeles, Calif (J.S.S.).
Radiol Cardiothorac Imaging. 2021 Oct 28;3(5):e200550. doi: 10.1148/ryct.2021200550. eCollection 2021 Oct.
Kawasaki disease (KD) is an inflammatory autoimmune vasculitis affecting the coronary arteries of very young patients, which can result in coronary artery aneurysms (CAAs) with lifelong manifestations. Accurate identification and assessment of CAAs in the acute phase and sequentially during the chronic phase of KD is fundamental to the treatment plan for these patients. The differential diagnosis of CAA includes atherosclerosis, other vasculitic processes, connective tissue disorders, fistulas, mycotic aneurysms, and procedural sequelae. Understanding of the initial pathophysiology and evolutionary arterial changes is important to interpretation of imaging findings. There are multiple applicable imaging modalities, each with its own strengths, limitations, and role at various stages of the disease process. Coronary CT angiography is useful for evaluation of CAAs as it provides assessment of the entire coronary tree, CAA size, structure, wall, and lumen characteristics and visualization of other cardiothoracic vasculature. Knowledge of the natural history of KD, the spectrum of other conditions that can cause CAA, and the strengths and limitations of cardiovascular imaging are all important factors in imaging decisions and interpretation. Pediatrics, Coronary Arteries, Angiography, Cardiac © RSNA, 2021.
川崎病(KD)是一种炎症性自身免疫性血管炎,影响极年幼患者的冠状动脉,可导致冠状动脉瘤(CAA)并伴有终身症状。在KD的急性期以及随后的慢性期准确识别和评估CAA,对于这些患者的治疗方案至关重要。CAA的鉴别诊断包括动脉粥样硬化、其他血管炎过程、结缔组织疾病、瘘管、霉菌性动脉瘤和手术后遗症。了解初始病理生理学和动脉演变变化对于解读影像学表现很重要。有多种适用的影像学检查方法,每种方法在疾病过程的不同阶段都有其自身的优势、局限性和作用。冠状动脉CT血管造影术对评估CAA很有用,因为它可以评估整个冠状动脉树、CAA的大小、结构、壁和管腔特征,并能显示其他心胸血管系统。了解KD的自然病史、可导致CAA的其他病症范围以及心血管成像的优势和局限性,都是影响成像决策和解读的重要因素。儿科学、冠状动脉、血管造影术、心脏 © RSNA,2021年