ArticleRespirology case reports2025
Idiopathic Pulmonary Haemorrhage, Is It Really Idiopathic?
Article in Respirology case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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2 authors.
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Abstract
Idiopathic pulmonary haemorrhage (IPH) is a rare cause of haemoptysis that most commonly presents in children. By definition, this condition is idiopathic in nature, however, exclusion of autoimmune capillaritis creates a diagnostic challenge. If autoimmunity is present, treatment is with immunosuppression. We present a 4-year-old girl with the classic clinical triad of IPH with haemoptysis, bilateral pulmonary infiltrate on chest radiography and iron deficiency anaemia. Her clinical course was complicated by frequent relapses in symptoms and critical pulmonary haemorrhage despite standard treatment for IPH. Successful remission of disease was induced with rituximab despite the absence of serological or lung biopsy evidence of autoimmune capillaritis.
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