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法洛四联症患儿的原发性肺动脉血栓形成

Primary thrombosis of pulmonary artery in a child with tetralogy of Fallot.

作者信息

Svane S

出版信息

Br Heart J. 1977 Jul;39(7):815-9. doi: 10.1136/hrt.39.7.815.

Abstract

A 34-month-old child with tetralogy of Fallot developed an acute, primary thrombosis of the pulmonary trunk. A greatly increased haematocrit was most probably a predisposing factor. An unusual postmortem finding was the large number of extremely dilated myocardial capillaries. In a review of a series of 394 consecutive necropsy cases with many kinds of cardiac anomalies, there was only one case (a 28-year-old man) with occluding thrombus formation in the pulmonary artery. This case also belonged to the Fallot group but a subacute glomerulonephritis seemed to be the major cause of death.

摘要

一名患有法洛四联症的34个月大儿童发生了肺动脉主干急性原发性血栓形成。血细胞比容大幅升高很可能是一个诱发因素。一个不寻常的尸检发现是大量极度扩张的心肌毛细血管。在对一系列连续394例患有多种心脏异常的尸检病例进行回顾时,仅有1例(一名28岁男性)在肺动脉中形成了阻塞性血栓。该病例也属于法洛四联症组,但亚急性肾小球肾炎似乎是主要死因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d6/483322/f143fd6651f4/brheartj00233-0118-a.jpg

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