Interstitial lung disease in rheumatoid arthritis: Current concepts in pathogenesis, diagnosis and therapeutics

doi:10.5499/wjr.v5.i1.1

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Mar 12, 2015 (publication date) through Jan 20, 2025

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World Journal of Rheumatology

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2220-3214

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Rheumatol. Mar 12, 2015; 5(1): 1-22
Published online Mar 12, 2015. doi: 10.5499/wjr.v5.i1.1

Table 4 Histological and clinical classification of idiopathic interstitial pneumonias

Histologic pattern	Clinical-Radiological-Pathological Diagnosis
Usual interstitial pneumonia	Idiopathic pulmonary fibrosis/COP
NSIP	NSIP
Organizing pneumonia	COP
Diffuse alveolar damage	Acute interstitial pneumonia
LIP	LIP

From: ref.[107], American Thoracic Society; European Respiratory Society. Am J Respir Crit Care Med 2002; 165: 277-304. COP: Cryptogenic fibrosing alveolitis; NSIP: Non-specific interstitial pneumonia; LIP: Lymphoid interstitial pneumonia.

Citation: Olivas-Flores EM, Bonilla-Lara D, Gamez-Nava JI, Rocha-Muñoz AD, Gonzalez-Lopez L. Interstitial lung disease in rheumatoid arthritis: Current concepts in pathogenesis, diagnosis and therapeutics. World J Rheumatol 2015; 5(1): 1-22
URL: https://www.wjgnet.com/2220-3214/full/v5/i1/1.htm
DOI: https://dx.doi.org/10.5499/wjr.v5.i1.1