Primary Pulmonary Hypertension

Author:

CHAPMAN DON W.1,ABBOTT JACK P.1,LATSON JOSEPH1

Affiliation:

1. From the Departments of Medicine and Pathology, Baylor University College of Medicine, Houston, Tex.

Abstract

A brief historical review of primary pulmonary arteriosclerosis and hypertension has been given. Ten additional cases with detailed laboratory, roentgenographic, electrocardiographic, cardiac catheterization, and angiocardiographic studies are presented. The findings on 4 necropsied cases are also included. Progressive exertional shortness of breath, syncope, left chest pain, right ventricular hypertrophy, and pulmonary arterial dilatation, combined with high right ventricular and pulmonary arterial pressure and normal pulmonary capillary pressure in the absence of pulmonary disease, should be extremely suggestive of primary pulmonary hypertension. An unrelenting downhill course of right ventricular failure is usually seen.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference22 articles.

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5. Cited by Warthin, A. S.: A case of Ayerza's Disease: Chronic cyanosis, dyspnea, and erythremia, associated with syphilitic arteriosclerosis of the pulmonary arteries;MARTY C. A.;Tr. A. Am. Physicians,1919

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