论文部分内容阅读
真性红细胞增多症临床上不多见;我国从1957年开始报道,至1965年前国内仅有15例,至1982年底全国已逾百例。最近,我们遇见两例,均以偏瘫为首发症状。初期按脑血栓形成常规治疗,疗效不佳;经骨髓穿刺证实本病后,针对病因治疗,病情明显好转,为提高临床诊治水平,兹总结报告如下。例1 王×,男,62岁,工人,住院号:34493。以头痛、眩晕、血压升高5年,短暂性发作性肢体乏力1年,左上下肢瘫痪1周,于1976年4月入院。
Polycythemia vera is rare in clinical practice; our country began to report from 1957 to 1965 before the domestic only 15 cases, by the end of 1982 more than 100 cases across the country. Recently, we met two cases, both hemiplegia as the first symptom. Initial cerebral thrombosis conventional treatment, poor efficacy; confirmed by the bone marrow puncture after the disease, for the cause of treatment, the condition was significantly improved, in order to improve the clinical diagnosis and treatment, it is summarized as follows. Example 1 Wang ×, male, 62 years old, workers, hospital number: 34493. To headache, dizziness, blood pressure increased 5 years, transient episodes of limb weakness for 1 year, left upper limb paralysis for 1 week, in 1976 April admission.