ELI H. RUBIN, M.D., F.A.C.P.; BERNARD S. KAHN, M.D.; DAVID PECKER, M.D.
This content is PDF only. Please click on the PDF icon to access.
In 1944 Hamman and Rich1 reported the histories and autopsy findings of four patients whose disease was characterized by a relatively sudden onset of dyspnea, cough, cyanosis and fever, and early signs of cardiac decompensation. Death resulted within a short time of acute pulmonary suffocation or heart failure. The lungs at autopsy revealed diffuse interstitial fibrotic changes of a type which the authors had never seen previously. They were unable to find any similar cases reported in the literature, with the exception of one instance of interstitial pulmonary fibrosis associated with lesions of periarteritis nodosa, by Kneeland and Smetana.2
RUBIN EH, KAHN BS, PECKER D. DIFFUSE INTERSTITIAL FIBROSIS OF THE LUNGS1. Ann Intern Med. 1952;36:827–844. doi: 10.7326/0003-4819-36-3-827
Download citation file:
Published: Ann Intern Med. 1952;36(3):827-844.
Interstitial Lung Disease, Pulmonary/Critical Care.
Results provided by:
Copyright © 2019 American College of Physicians. All Rights Reserved.
Print ISSN: 0003-4819 | Online ISSN: 1539-3704
Conditions of Use