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  • Title: Idiopathic pulmonary haemosiderosis--a case report.
    Author: Ng SC, Lee BW, Chia F.
    Journal: Singapore Med J; 1998 May; 39(5):211-6. PubMed ID: 9713227.
    Abstract:
    Idiopathic pulmonary haemosiderosis (IPH) is a disorder characterised by the triad of haemoptysis, diffuse parenchymal infiltrates on chest roentgenogram and iron-deficiency anaemia. It is a diagnosis of exclusion and the prognosis is bleak despite the varied management options. We report a case of IPH occurring in a child who presented at four months of age with cough, wheeze, haemoptysis and pallor and whose symptoms are currently controlled with high-dose inhaled budesonide and low-dose oral prednisolone.
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