Hypersensitivity pneumonitis


Pneumoconiosis (Pulmonary Fibrosis)




Extrinsic allergic alveolitis

Biomedical References

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Acute presentation: flu-like illness with cough; Subacute: recurrent "pneumonia"; Chronic: exertional dyspnea, productive cough, and weight loss; Most patients have abnormal imaging studies (chest x-ray or high-resolution CT). Crepitant rales are heard in some cases. Pulmonary function testing shows a restrictive defect in early disease and a restrictive, obstructive or mixed defect in late disease. Precipitating antibodies are neither sensitive nor specific, and their presence is no longer considered a hallmark of HP. Some patients have decreased diffusion capacity and arterial hypoxemia. If the diagnosis is in doubt, bronchoalveolar lavage (BAL) typically shows lymphocytosis. Surgical lung biopsy may be indicated if bronchoscopy is nondiagnostic. The disease latency varies from a few weeks to years after first exposure. Symptoms appear or worsen within a few hours of antigen exposure to bioaerosols of microbial or animal antigens or rarely to a few reactive chemicals. Complete recovery usually occurs if exposure is terminated early. Otherwise, the disease may progress to interstitial fibrosis. [Murray, p. 1783-1799] From 1980 -2002 in the US, 814 deaths from HP were identified. Of these 814 cases, 56% were unspecified in type, 37% were farmer's lung, 4% bird fancier lung, 1% bagassosis, 1% humidifier lung, and 1 case each for mushroom worker lung and maple bark stripper lung. [Hyperlink]


Weeks to years until "sensitized"; acute symptoms 4-12 hours after exposure;


Clinical; Chest x-ray; HRCT; Pulmonary function testing; BAL; Lung biopsy;

ICD-9 Code


Reference Link

Twenty-three years of hypersensitivity pneumonitis...[Am J Ind Med. 2006] - PubMed Result

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