| Literature DB >> 884033 |
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.Entities:
Mesh:
Year: 1977 PMID: 884033 PMCID: PMC483322 DOI: 10.1136/hrt.39.7.815
Source DB: PubMed Journal: Br Heart J ISSN: 0007-0769