Image of Idiopathic Pulmonary Fibrosis.

LITERATURE

Idiopathic Pulmonary Fibrosis.


The family of interstitial lung diseases is characterized by cellular proliferation, interstitial inflammation, fibrosis, or a combination
of such findings within the alveolar wall that is not due to infection or cancer.1 Interstitial fibrosis is the predominant phenotype in most cases. The majority of patients with interstitial fibrosis ultimately receive a diagnosis of chronic hypersensitivity pneumonitis (due to mold or bird exposure), pulmonary sarcoidosis, an underlying autoimmune disease, or if no cause is identified, an idiopathic interstitial pneumonia.


Availability

REQJ776Available

Detail Information

Series Title
-
Call Number
-
Publisher : .,
Collation
-
Language
English
ISBN/ISSN
-
Classification
NONE
Content Type
-
Media Type
-
Carrier Type
-
Edition
-
Subject(s)
Specific Detail Info
N Engl J Med 2018;378:1811-23.
Statement of Responsibility

Other version/related

No other version available


File Attachment



Information


RECORD DETAIL


Back To Previous