Abstract
Interstitial pulmonary fibrosis and tracheobronchial sicca are the most common presentation of pulmonary involvement in primary Sjögren's syndrome. There is wide spectrum of less common manifestations, including pulmonary arterial hypertension, pseudolymphoma, pulmonary lymphoma, lymphocytic interstitial pneumonitis, amyloidosis, and pleurisy. Pulmonary function test abnormalities showing a restrictive pattern and cellular abnormalities in bronchoalveolar lavage fluid for prevalent in patients without respiratory complaints and normal chest radiographs. Long-term prospective controlled studies are needed to determine the clinical course and significance of these findings.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Amyloidosis / pathology
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Bronchial Diseases / diagnosis
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Bronchial Diseases / pathology
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Bronchial Diseases / physiopathology
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Bronchoalveolar Lavage Fluid / cytology
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Controlled Clinical Trials as Topic
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Humans
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Hypertension, Pulmonary / pathology
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Longitudinal Studies
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Lung / physiopathology
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Lung Diseases, Interstitial / pathology
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Lung Neoplasms / pathology
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Lymphocytes / pathology
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Lymphoma / pathology
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Pleurisy / pathology
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Prevalence
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Prospective Studies
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Pseudolymphoma / pathology
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Pulmonary Fibrosis / diagnosis
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Pulmonary Fibrosis / pathology*
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Pulmonary Fibrosis / physiopathology
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Sjogren's Syndrome / diagnosis
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Sjogren's Syndrome / pathology*
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Sjogren's Syndrome / physiopathology
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Tracheal Diseases / diagnosis
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Tracheal Diseases / pathology
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Tracheal Diseases / physiopathology