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Published byKristin Hubbard Modified over 9 years ago
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Esam H. Alhamad, M.D Assistant Professor of Medicine Consultant Pulmonary & Critical Care Medicine
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ATS/ERS. Am J Respir Crit Care Med 2002;165:277-3
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INTERSTITIAL LUNG DISEASE Hypersensitivity Pneumonia Idiopathic pulmonary Fibrosis Smoking Associated ILD
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Hypersensitivity Pneumonia Antigens Mammalian and avian protein Fungi Thermophilic bacteria Certain small molecular weight compounds
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CLINCAL FORMS ACUTE SUBACUTE CHRONIC
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ACUTE FORM Symptoms appear 4-8 hour after exposure Fever, chills, malaise, tightness of the chest cough, dyspnea, expectoration, headache Symptoms gradually decrease over the next 24-48 hours, but recur after next exposure
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SUBACUTE/CHRONIC FORMS Continuous low-level antigen exposure (e.g few birds at home) Insidious onset of the disease Duration of symptoms 2-24 months
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SUBACUTE/CHRONIC FORMS Chronic progressive dyspnea Fatigue, poor appetite, weight loss Cough with mucoid sputum Occasional digital clubbing May progress to fibrosis, respiratory failure, cor pulmonale
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CHEST X-RAY & HRCT Ground glass opacities Poorly defined micronodules Patchy air space opacification Fine and coarse reticular opacities Honeycombing ( chronic advanced cases)
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PULMONARY FUNCTION TESTS Restrictive, obstructive, or mixed defect Most common finding Dlco 40% airflow obstruction Emphysema more common than fibrosis Alhamad et al. Clin Chest Med 2001; 22:715-750
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BRONCHOALVEOLR LAVAGE T lymphocytes ~ 50% CD8+ T-cells CD4+ T-cells CD4+/CD8+ ratio CD4+/ CD8+ ratio
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LUNG BIOPSY Lymphocytes infiltration Granuloma Bronchiolitis Emphysema Fibrosis
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DIAGNOSIS Clinical, radiologic and functional abnormalities suggestive of an I.L.D History of exposure to HP antigens Positive specific antibodies Lung biopsy Hypersensitivity pneumonitis
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THERAPY Avoidance of antigen exposure Corticosteroids
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