[Idiopathic pulmonary hemosiderosis in adults]
- PMID: 16012364
- DOI: 10.1016/s0761-8417(05)84796-0
[Idiopathic pulmonary hemosiderosis in adults]
Abstract
Idiopathic pulmonary hemosiderosis (IPH) is a rare cause of diffuse alveolar hemorrhage characterized by abnormal deposition of hemosiderin iron in the macrophages of alveoli. Most cases occur in children. In adults, IPH is rare: almost 10 cases reported during the late 10 years. We report the case of a 20-year-old-girl with IPH. There was no evidence of pulmonary vasculitis or capillaritis. Long-term treatment with systemic corticosteroids was followed by clinical remission lasting 4 years.
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