论文部分内容阅读
柴某,男,47岁,1985年9月开始乏力,头暈、低烧。查体:胸骨无压痛,肝肋卜3 cm,脾大肋下3 cm。血常规:Hb12.5g,WBC58000/mm~3,淋巴11％,嗜碱粒4％,原早粒5％,中幼粒11％,晚幼粒17％,杆状核21％,分叶核3％。血小板44.4万/mm~3。骨髓增生明显活跃,粒红比增高(87.5:1),分类中晚杆均明显增高。诊断慢粒,给马利兰、靛玉红治疗,症状渐消失,维持半年余.1986年4月患者高热不退,脾进行性增大至肋下9 cm。骨髓增生明显活跃,原幼淋
Chai Mou, male, 47 years old, started in September 1985 fatigue, dizziness, fever. Physical examination: no tenderness of the sternum, liver ribs BU 3 cm, splenic ribs 3 cm. Blood: Hb12.5g, WBC58000 / mm ~ 3, lymphatic 11%, basophilic 4%, 5% of the original early grain, 11% of the young, young juvenile 17%, 21% 3%. 444,000 platelets / mm ~ 3. Myeloid hyperplasia was obviously active, the ratio of granulocytes to erythrocyte increased (87.5: 1), and the classification of middle and late pole were significantly higher. Diagnosis of CML, to Maryland, indirubin treatment, the symptoms gradually disappear, more than six months to maintain .1986 in April patients with high fever, splenic progressively increased to the ribs 9 cm. Myeloid hyperplasia was significantly active, the original baby shower