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・ Idiopathic facial aseptic granuloma
・ Idiopathic generalized epilepsy
・ Idiopathic giant-cell myocarditis
・ Idiopathic granulomatous hepatitis
・ Idiopathic guttate hypomelanosis
・ Idiopathic hypersomnia
・ Idiopathic hypoglycemia
・ Idiopathic infantile arterial calcification
・ Idiopathic interstitial pneumonia
・ Idiopathic intracranial hypertension
・ Idiopathic orbital inflammatory disease
・ Idiopathic osteosclerosis
・ Idiopathic pneumonia syndrome
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Idiopathic pulmonary haemosiderosis
・ Idiopathic pure sudomotor failure
・ Idiopathic sclerosing mesenteritis
・ Idiopathic scrotal calcinosis
・ Idiopathic short stature
・ Idiopathic thrombocytopenic purpura
・ Idiopathy
・ Idiophantis
・ Idiophantis acanthopa
・ Idiophantis anisosticta
・ Idiophantis callicarpa
・ Idiophantis carpotoma
・ Idiophantis chalcura
・ Idiophantis chiridota
・ Idiophantis croconota


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Idiopathic pulmonary haemosiderosis : ウィキペディア英語版
Idiopathic pulmonary haemosiderosis

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. It is rare, with an incidence between 0.24〔 and 1.23〔 cases per million people.
==History==
The condition was first described as "brown lung induration" by Rudolf Virchow in 1864 in patients after their death. Wilhelm Ceelen later correlated his findings to the clinical symptoms of two children who died of IPH in 1931.〔 The first living patient was diagnosed by Jan Waldenström in 1944.〔 It has been given several names, including:
*Haemosiderin accumulation
*Pulmonary haemosiderosis
*Brown induration of lung
*Essential brown induration of lung
*Ceelen-Gellerstedt syndrome (after physicians Wilhelm Ceelen and Nils Gellerstedt)〔

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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