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婴幼儿及儿童冠状动脉瘤。文献综述及6例报告。

Aneurysms of the coronary arteries in infants and children. A review, and report of six cases.

作者信息

Aterman K, Dische M R, Franke J, Fraser G M, Meyer W W

出版信息

Virchows Arch A Pathol Anat Histol. 1977 May 13;374(1):27-44. doi: 10.1007/BF00430568.

Abstract

In recent years large numbers of the so-called "mucocutaneous lymph node syndrome" or "Kawasaki's disease" have been described by Japanese workers, but instances of this disorder are only now being reported as isolated cases by European or North American physicians. The disease has, therefore, been considered to be a new entity. One of its most striking features is the development of aneurysms of the coronary arteries in infants or children, which may lead to sudden death. Aneurysms of the coronary arteries in childhood are rare, and hence it was considered relevant to report six such cases, and to examine their possible relationship to Kawasaki's disease. The pathological changes underlying the latter disorder are not well known; they are considered to be indistinguishable from infantile polyarteritis nodosa. A diagnosis of polyarteritis nodosa was also thought to be most likely to apply in the cases presented here, particularly in view of the frequency with which aneurysms of the coronary arteries have been found in this disorder. In the absence of valid pathological distinctions between Kawasaki's disease and infantile polyarteritis nodosa, the question arises whether these entities are, in fact, different, and whether Kawasaki's disease is the new entity it is assumed to be.

摘要

近年来,日本学者报道了大量所谓的“黏膜皮肤淋巴结综合征”或“川崎病”,但欧洲或北美医生目前才开始将这种疾病作为个别病例进行报告。因此,该病被认为是一种新的疾病实体。其最显著的特征之一是婴儿或儿童冠状动脉瘤的形成,这可能导致猝死。儿童期冠状动脉瘤较为罕见,因此报告6例此类病例并研究它们与川崎病的可能关系被认为是有意义的。川崎病的病理变化尚不清楚,一般认为与婴儿结节性多动脉炎难以区分。结节性多动脉炎的诊断在此处呈现的病例中也被认为是最有可能适用的,特别是考虑到在这种疾病中发现冠状动脉瘤的频率。鉴于川崎病和婴儿结节性多动脉炎之间缺乏有效的病理区别,问题就出现了,即这些疾病实体实际上是否不同,以及川崎病是否真的是人们所认为的那种新的疾病实体。

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