Lymphoid interstitial pneumonia

MONDO:0009537

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.

Also known as: diffuse hyperplasia of bronchus-associated lymphoid tissue, lymphocytic interst. pneumonitis, lymphocytic interstitial pneumonia, lymphocytic interstitial pneumonitis, lymphoid interstitial pneumonia, LIP

113 clinical trials for this condition and its sub-types.

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