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过去,急性颗粒性白血球減少症的死亡率是很高的,特別在白血球总数低于1,000或中性白血球低于10％者,如治疗不能及时及治疗不充分时,死亡率可高达70％左右。本院58年5-9月份,先后收治本病三例,入院后均經采用髂骨輸入骨髓方法治疗,平均每人輸入骨髓3至4次(骨髓10毫升)后8至23天血象恢复正常而痊愈,特报告于后,供同道参考。簡約病历介紹: 例一:許××,男,26岁,业农,住院号4719,初为头痛,低热,喉及牙痛,至5月24日病情恶化,恶寒高燒,体温弛张于38-40.5℃,咽及扁桃体紅肿潰烂,心肺阴性,肝脾未能捫及,白血球1600,中性12％,淋巴88％。經先后輸骨髓4次,共10.5毫升后三周症状消失,40天痊愈。
In the past, the mortality rate of acute granulocytic leucopenia was high, especially when the total number of leukocytes was less than 1,000 or less than 10% of neutrophils. If the treatment can not be timely and the treatment is inadequate, the mortality rate can reach about 70% . Our hospital from May to September 58, has treated the disease in three cases, after admission were treated with iliac bone marrow input method, the average input of bone marrow 3 to 4 times (bone marrow 10 ml) 8 to 23 days after the blood returned to normal And heal, especially after the report, for fellow reference. Simple case description: Example 1: Xu × ×, male, 26 years old, farming, hospital number 4719, early headache, fever, throat and toothache, to May 24 the condition deteriorated, aversion to cold and fever, temperature relaxation in 38 -40.5 ℃, swollen pharynx and tonsil ulcers, heart and lung negative, liver and spleen failed palpable, white blood cells 1600, 12% of neutral, lymphatic 88%. Bone marrow has been lost 4 times, a total of 10.5 ml after three weeks the symptoms disappear, 40 days cured.