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粒细胞缺乏症是一种起病急骤,经过和预后均较严重的血液病,其病因复杂,发病机理不一。临床以药物和化学品引起者多见。本文总结我院内科自1960～1978年收治的粒细胞缺乏症30例临床资料,分析如下。一、一般资料男12例(40%),女18例(60%),男女之比为1∶1.5,年龄自15～58岁,其中21～40岁者20例(66.6%),青壮年居多。二、临床表现起病急,多有发热及全身症状。(表1)
Agranulocytosis is a sudden onset, the prognosis is more serious blood diseases, its etiology is complex, the pathogenesis is different. Clinical medicine and chemicals caused more common. This article summarizes the clinical data of 30 cases of agranulocytosis admitted to our hospital from 1960 to 1978, analyzed as follows. First, the general information of 12 males (40%), 18 females (60%), male to female ratio of 1: 1.5, aged 15 to 58 years old, of which 21 to 40 years old in 20 cases (66.6% Mostly. Second, the clinical manifestations of acute onset, more fever and systemic symptoms. (Table 1)