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特发性肺含铁血黄素沉着症(Idiopathic Pulmonary hemosiderosis简称IPH),本病较少见,我院儿科从1974～1985年共收治22例,多数长期误诊、漏诊,说明提高对本病的认识很有必要。一、一般资料性别,男10例,女12例。年龄:1 2/12岁1例,7~12岁10例。婴儿期喂养史有记录15例:母乳喂养7例,洲恍合喂养8例,均无牛奶过敏及遗传病史。二、入院症伏以呼吸进症状为主10例,以贫血症状为主12例。发作期:发热21例,咳嗽20例,咯血16例,呼吸困难2例,发纷2例,腹痛2例,肺部湿鸣3例,肝肿大6例,脾肿太再例,肝脾钟大4例,杆交黄疽1例,杆状指1俩
Idiopathic pulmonary hemosiderosis (Idiopathic Pulmonary hemosiderosis referred to as IPH), the disease is rare, our hospital from 1974 to 1985, a total of 22 cases were treated, the majority of long-term misdiagnosis, missed diagnosis, to improve awareness of the disease necessary. First, the general information of gender, 10 males and 12 females. Age: 1 2/12 years in 1 case, 7 to 12 years in 10 cases. There were 15 cases of infantile feeding history: breastfeeding in 7 cases, Chau Hop feeding in 8 cases, no milk allergy and genetic history. Second, admission to V-induced respiratory symptoms in 10 cases, mainly anemia in 12 cases. Episodes: fever in 21 cases, 20 cases of cough, hemoptysis in 16 cases, dyspnea in 2 cases, 2 cases of sporadic, abdominal pain in 2 cases, 3 cases of lung dampness, hepatomegaly in 6 cases, splenomegaly too much case, liver and spleen Big bell in 4 cases, rod jaundice in 1 case, rod refers to two