Idiopathic pulmonary haemosiderosis--a case report

Singapore Med J. 1998 May;39(5):211-6.

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.

Publication types

  • Case Reports

MeSH terms

  • Anti-Inflammatory Agents / therapeutic use
  • Budesonide / therapeutic use
  • Drug Therapy, Combination
  • Hemosiderosis* / diagnosis
  • Hemosiderosis* / drug therapy
  • Humans
  • Infant
  • Lung Diseases / diagnosis
  • Lung Diseases / drug therapy
  • Male
  • Prednisolone / therapeutic use
  • Prognosis

Substances

  • Anti-Inflammatory Agents
  • Budesonide
  • Prednisolone