idiopathic pulmonary haemosiderosis , IPH (skrót)

Idiopathic pulmonary haemosiderosis can occur either as a primary lung disorder or as the sequela to other pulmonary, cardiovascular or immune system disorder.

Idiopathic pulmonary haemosiderosis (or idiopathic pulmonary hemosiderosis; IPH) is a lung disease of unknown cause that is characterized by alveolar capillary bleeding and accumulation of haemosiderin in the lungs.

Kubba and Young have pointed out a number of other conceivable, if unlikely, diagnoses, besides cystic fibrosis and alfa 1-antitripsin deficiency: Churg-Strauss syndrome, allergic bronchopulmonary aspergillosis, hypogammaglobulinemia, idiopathic pulmonary haemosiderosis, lung abscesses, and pulmonary arteriovenous malformations.