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川崎病合并巨大动脉瘤患者的多模态心脏成像

Multimodality Cardiac Imaging in a Patient with Kawasaki Disease and Giant Aneurysms.

作者信息

Srinivasan Ranjini, Weller Rachel, Chelliah Anjali, Einstein Andrew J

机构信息

Department of Pediatrics, Division of Pediatric Cardiology, Columbia University Medical Center and Morgan Stanley Children's Hospital of New York-Presbyterian, New York, NY, USA.

Department of Medicine, Division of Cardiology, Columbia University Medical Center and New York-Presbyterian Hospital, New York, NY, USA; Department of Radiology, Columbia University Medical Center and New York-Presbyterian Hospital, New York, NY, USA.

出版信息

Case Rep Pediatr. 2016;2016:4298098. doi: 10.1155/2016/4298098. Epub 2016 Oct 31.

Abstract

Kawasaki disease is a well-known cause of acquired cardiac disease in the pediatric and adult population, most prevalent in Japan but also seen commonly in the United States. In the era of intravenous immunoglobulin (IVIG) treatment, the morbidity associated with this disease has decreased, but it remains a serious illness. Here we present the case of an adolescent, initially diagnosed with Kawasaki disease as an infant, that progressed to giant aneurysm formation and calcification of the coronary arteries. We review his case and the literature, focusing on the integral role of multimodality imaging in managing Kawasaki disease.

摘要

川崎病是儿童和成人后天性心脏病的一个知名病因,在日本最为普遍,但在美国也很常见。在静脉注射免疫球蛋白(IVIG)治疗时代,与这种疾病相关的发病率有所下降,但它仍然是一种严重疾病。在此,我们介绍一名青少年的病例,该患者婴儿期最初被诊断为川崎病,后来发展为巨大动脉瘤形成和冠状动脉钙化。我们回顾他的病例及相关文献,重点关注多模态成像在川崎病管理中的重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ce/5107831/68c4bb192693/CRIPE2016-4298098.001.jpg

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