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特发性肺含铁血黄素沉着症(Idiopathic pulmonary hemosiderosis,简称IPH)为一种少见的、病因不详的疾病,多发生于小儿时期,可能与自身免疫有关。其临床特征为咳嗽、咳血、贫血。现将我区报道的9例及河南省宁陵县医院1例综合报告如下:
Idiopathic pulmonary hemosiderosis (Idiopathic pulmonary hemosiderosis, referred to as IPH) is a rare disease of unknown etiology, mostly in infancy, may be related to autoimmunity. The clinical features of cough, hemoptysis, anemia. Now I reported in 9 cases and Ningling County Hospital in Henan Province, a comprehensive report is as follows: