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特发性肺含铁血黄素沉着症(简称IPH)系肺泡内毛细血管反覆出血引起含铁血黄素在肺泡内沉积,导致肺间质纤维化,影响肺功能,继而造成肺动脉高压、右心衰竭。此病自1864年Virchow首次报道后,已有不少病例报道。现将24例原发性肺含铁血黄素沉着症综合报道如下。
Idiopathic pulmonary hemosiderosis (referred to as IPH) Department of alveolar capillaries repeated bleeding caused by hemosiderin deposition in the alveoli, leading to interstitial lung fibrosis, affecting lung function, resulting in pulmonary hypertension, right heart failure . Since the Virchow first reported in 1864, many cases have been reported. Now 24 cases of primary pulmonary hemosiderosis comprehensive report is as follows.