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KMID : 0391119930020020149
Ulsan University Medical Journal
1993 Volume.2 No. 2 p.149 ~ p.155
A Case of Idiopathic Pulmonary Hemosiderosis
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Abstract
Idiopathic pulmonary hemosiderosis(IPH) is a relatively rare disease of unknown etiology characterized pathologically by recurrences of intraalveolar pulmonary hemorrhage.
Clinical features include hemoptysis, iron deficiency anemia and pulmonary parenchymal infiltrations on chest radiograph. Hemosiderin-laden macrophages are demonstrated by examination of sputum or lung biopsy specimens.
We diagnosed IPH by lung biopsy in 9 year-old girl who had had recurrent hemoptysis, iron deficiency anemia and diffuse pulmonary infiltrates on chest radiograph and report this case with brief literature review.
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