Lymphocytic interstitial pneumonitis

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 - interstitial pneumonia characterized by the presence of bibasilar pulmonary interstitial infiltrates composed of lymphocytes and plasma cells. It may be associated with autoimmune and lymphoproliferative disorders. Signs and symptoms include fever, cough, and dyspnea. Symptomatic patients may require immunosuppressive treatment.

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Source: Data courtesy of the U.S. National Library of Medicine. Since the data might have changed, please query MeSH on Lymphocytic interstitial pneumonitis for any updates.

 

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