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特发性肺含铁血黄素沉着症(IPH)是一组原因不明,以选择性肺内含铁血黄素沉着为特征的肺毛细血管出血性疾病。因该病少见,临床表现复杂,易造成误诊。本文综合报告我院1977—1986年确诊的4例 IPH 患者。4例临床资料见表.
Idiopathic pulmonary hemosiderosis (IPH) is a group of pulmonary capillary hemorrhagic diseases with unknown cause and selective pulmonary hemosiderosis. Because of the rare disease, the clinical manifestations of complex, easily lead to misdiagnosis. This article comprehensive report our hospital from 1977 to 1986 confirmed 4 cases of IPH patients. 4 cases of clinical information in the table.