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1981年4月至1987年3月经本科收治及确诊的特发性肺含铁血黄素沉着症(Idiopathic Pulmonary hemosiderosis,简称IPH),均曾较长时期在院内外被误诊,现将其临床资料作简要报告,并分析误诊原因,以引起重视。临床资料一、一般资料:9例中男3例,女6例,发病年龄1岁半～7岁,平均4岁。主要症状、体征:苍白9例,发热、咳嗽、咯血各7例,乏力5例,头晕、异嗜癖各3例,腹痛、气急各2例。右锁骨中线肋缘下肝脏大小:4岁前的4例分别为未及、
From April 1981 to March 1987, idiopathic pulmonary hemosiderosis (Idiopathic Pulmonary Hemosiderosis, IPH), admitted and diagnosed by our department, were misdiagnosed both in and outside the hospital for a long time. The clinical data Brief report, and analyze the causes of misdiagnosis, in order to attract attention. Clinical data First, the general information: 9 cases of 3 males and 6 females, the age of onset of 1 year and a half to 7 years old, with an average of 4 years old. The main symptoms and signs: pale 9 cases, fever, cough, hemoptysis in 7 cases, 5 cases of fatigue, dizziness, addiction each 3 cases, abdominal pain, shortness of breath in 2 cases. Right subclavian midline rib margin liver size: 4 cases before the age of 4, respectively,