近年来,特发性肺含铁血黄素沉着症(简称IPH)的临床病例报道较多,而对远期疗效报告尚少。本文对7例IPH病儿进行了5～14年随访,并对呼吸功能进行检测,现将结果报告如下。临床资料入院时病情:本院自1972～1985年共收治10名IPH患儿,根据王氏诊断标准进行诊断。10例均有反复的间断咳嗽、血痰或咯血、贫血,陶片均呈急性肺泡出血的改变,如毛玻璃状、粟粒结节状的细小 In recent years, the clinical cases of idiopathic pulmonary hemosiderosis (referred to as IPH) reported more, while the long-term efficacy of the report is still small. In this paper, 7 cases of IPH sick children were followed up for 5 to 14 years, and respiratory function testing, the results reported below. Clinical data admission condition: hospital from 1972 to 1985, a total of 10 children with IPH were diagnosed according to Wang diagnostic criteria. 10 cases were repeated intermittent cough, bloody sputum or hemoptysis, anemia, were allantoic alveolar hemorrhage changes, such as ground glassy, ​​miliary nodular small