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原发性血小板减少性紫癜并发获得性溶血性贫血(Evans氏综合征)报道甚少,我院近期发现2例,报告如下。病例报告例1:谢×,女,17岁。1977年5月19日入院。入院前一月,突起苍黄乏力,头晕肢软,随即发现两下肢多数出血点及瘀斑,来院就诊。经骨穿诊断“紫癜”、“增生性贫血”收入院。患者既往身健,病前未用特殊药物。体检:贫
Primary thrombocytopenic purpura complicated with acquired hemolytic anemia (Evans’s syndrome) reported little, our hospital recently found in 2 cases, the report is as follows. Case Report 1: Xie ×, female, 17 years old. May 19, 1977 admission. One month before admission, sudden pale yellow weakness, dizziness, limbs, then found that most of the lower extremity bleeding and ecchymosis, to the hospital. Diagnosis of the bone by the “purpura”, “proliferative anemia” income hospital. The patient both healthy, ill before the use of special drugs. Physical examination: poor