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[川崎病的黏膜皮肤淋巴结综合征。1例并发多发性动脉瘤]

[The mucocutaneous and lymph node syndrome of Kawasaki. 1 case complicated by multiple aneurysms].

作者信息

Gorin R, Sorin M, Meyer A, Batisse A, Toumieux M C, Mozziconacci P

出版信息

Sem Hop. 1978 Apr;54(9-12):442-7.

PMID:28565
Abstract

We report in a five month old baby a case of the cutaneomucosal and lymph node syndrome described by Kawasaki, remarkable for the onset of multiple aneurysms involving the coronary and the limb arteries. This syndrome has rarely been observed except in Japan where it seems frequent. Possibly is benign forms, without heart complications, producing a picture of febrile erythema of viral type, have not received sufficient attention. The relationship between Kawasaki's disease and periarteritis nodosa in infants is then discussed. The clinical and pathological existence of the fatal forms seems undoubted, but the generally benign course of Kawasaki's disease contrasts with the severe course of polyarteritis nodosa in infants. It is possible that the usually benign forms of Kawasaki's disease represent only the initial stage of periarteritis nodosa in infants, from which they may recover, and we have only identified until now the severe forms which are rapidly fatal. The etiology of Kawasaki's syndrome, like periateritis nodosa remains unknown.

摘要

我们报告了一例5个月大婴儿患川崎描述的皮肤黏膜淋巴结综合征,其显著特征是出现累及冠状动脉和肢体动脉的多发性动脉瘤。除了在日本这种综合征似乎较为常见外,在其他地方很少观察到。可能是那些无心脏并发症、表现为病毒型发热性红斑的良性形式未得到足够关注。随后讨论了婴儿川崎病与结节性多动脉炎之间的关系。致命形式的临床和病理存在似乎是毋庸置疑的,但川崎病通常的良性病程与婴儿结节性多动脉炎的严重病程形成对比。有可能川崎病通常的良性形式仅代表婴儿结节性多动脉炎的初始阶段,患儿可能从中恢复,而我们迄今只识别出了迅速致命的严重形式。川崎综合征的病因,如同结节性多动脉炎一样,仍然不明。

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