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一名3个月大婴儿患结节性多动脉炎和先天性幽门肥厚。

Polyarteritis nodosa and congenital pyloric hypertrophy in a 3-month-old infant.

作者信息

SAVAGE T R, SMITH J F

出版信息

J Clin Pathol. 1960 Jul;13(4):291-6. doi: 10.1136/jcp.13.4.291.

Abstract

A case of polyarteritis nodosa in the first year of life with the clinical picture dominated by pyrexia, an initial upper respiratory element, episodes of tachycardia, and sudden death three weeks after the onset is described. The necropsy showed evidence of polyarteritis nodosa, myocarditis, and valvulitis as well as congenital pyloric hypertrophy. Clinical manifestations of the latter had preceded the final illness and the two diseases were not thought to be related. The previous 19 cases reported in the first year of life are reviewed, and support is given for the concept that at this age a rash, pyrexia, upper respiratory manifestations, and progressive heart failure or sudden death are characteristic clinical manifestations and that the heart is often the site of the major lesions at necropsy. The possible role of hypersensitivity is discussed. There was no evidence for it in the present case.

摘要

本文描述了一例一岁儿童结节性多动脉炎病例,其临床表现以发热、最初的上呼吸道症状、心动过速发作以及发病三周后突然死亡为主。尸检显示有结节性多动脉炎、心肌炎、瓣膜炎以及先天性幽门肥厚的证据。后者的临床表现先于最终疾病出现,且认为这两种疾病并无关联。对既往报道的19例一岁儿童结节性多动脉炎病例进行了回顾,支持了以下观点:在这个年龄段,皮疹、发热、上呼吸道表现以及进行性心力衰竭或猝死是其特征性临床表现,且尸检时心脏常是主要病变部位。文中还讨论了超敏反应可能起的作用。本病例中未发现相关证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b01f/480083/175e60ccf938/jclinpath00057-0015-a.jpg

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