Results 321 to 330 of about 654,309 (397)

Lymphocytic Interstitial Pneumonia.

Clinics in Chest Medicine, 2016
Lymphocytic interstitial pneumonia (LIP) is a rare lung disease on the spectrum of benign pulmonary lymphoproliferative disorders. LIP is frequently associated with connective tissue diseases or infections. Idiopathic LIP is rare; every attempt must be made to diagnose underlying conditions when LIP is diagnosed.
T. Panchabhai, C. Farver, K. Highland
semanticscholar   +4 more sources

Long‐term clinical course and outcome of interstitial pneumonia with autoimmune features

Respirology (Carlton South. Print), 2020
Idiopathic interstitial pneumonia (IIP) with autoimmune features that does not fulfil connective tissue disease (CTD) criteria has been recently defined as interstitial pneumonia with autoimmune features (IPAF). However, its long‐term clinical course and
H. Kim   +4 more
semanticscholar   +1 more source

Nonspecific Interstitial Pneumonia

Seminars in Respiratory and Critical Care Medicine, 2020
AbstractNonspecific interstitial pneumonia (NSIP) is a complex disorder commonly associated with other conditions such as connective tissue diseases (CTDs) and environmental exposures. Although idiopathic NSIP has been recognized as a separate clinical entity, recent studies have suggested that a proportion of these cases have autoimmune features ...
Alan K Y Teoh   +3 more
openaire   +3 more sources

Nonspecific Interstitial Pneumonia

Seminars in Respiratory and Critical Care Medicine, 2006
Nonspecific interstitial pneumonia (NSIP) describes a histopathologic pattern that can be seen in patients with immunodeficiency, drug or environmental exposures, and connective tissue diseases. The clinical diagnosis of NSIP, however, should be reserved for idiopathic cases in which no causative factor is identified.
Kevin R. Flaherty, Fernando J. Martinez
openaire   +3 more sources

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