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Nonspecific interstitial pneumonia.

Abstract
Traditionally, a subset of patients diagnosed as having idiopathic pulmonary fibrosis had positive results on cellular biopsies (prominent lymphoplasmacytic inflammation), bronchoalveolar lavage lymphocytosis, a clinical response to steroids, and a better long-term prognosis. On review of the lung histopathology, the lesion was characterized by varying degrees of inflammation and fibrosis. This entity is now recognized as a distinct entity among idiopathic interstitial pneumonias.
AuthorsBrent Wayne Kinder
JournalClinics in chest medicine (Clin Chest Med) Vol. 33 Issue 1 Pg. 111-21 (Mar 2012) ISSN: 1557-8216 [Electronic] United States
PMID22365250 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2012 Elsevier Inc. All rights reserved.
Chemical References
  • Adrenal Cortex Hormones
  • Anti-Inflammatory Agents
  • Immunosuppressive Agents
  • Cyclophosphamide
  • Mycophenolic Acid
  • Azathioprine
Topics
  • Adrenal Cortex Hormones (therapeutic use)
  • Anti-Inflammatory Agents (administration & dosage, therapeutic use)
  • Azathioprine (therapeutic use)
  • Biopsy (methods)
  • Cyclophosphamide (therapeutic use)
  • Diagnosis, Differential
  • Drug Administration Schedule
  • Drug Therapy, Combination
  • Humans
  • Idiopathic Interstitial Pneumonias (diagnosis, diagnostic imaging, drug therapy, pathology)
  • Idiopathic Pulmonary Fibrosis (diagnosis)
  • Immunosuppressive Agents (administration & dosage, therapeutic use)
  • Lung (pathology)
  • Mycophenolic Acid (analogs & derivatives, therapeutic use)
  • Tomography, X-Ray Computed
  • Treatment Outcome

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