论文部分内容阅读
恶性网细胞病从1957年国内田氏首次报告以来已有20年的历史,现将我们1966～1977年收治20例分析如下。一、临床资料本组病例男15例,女5例,男女之比3:1。年龄最小1岁,最大74岁,平均35岁,15～45岁占75％(15/20)。职业:工人8例,农民7例,干部2例,学生1例,无职业2例,工农占75％。症状和体征:发热20例,衰竭15例,贫血 14例,皮肤粘膜出血7例,巩膜皮肤黄染5例,皮肤结节2例,消化道出血8例,消化道穿孔2例,皮肤溃疡1例。肝肿大1.5厘米以下5例,1.5～3厘米8例,3～6厘米2例,无肿大5例,肝肿大率75％。脾肿大1.5厘米以下6例,1.5～3厘米3例,3～6厘米2例,脾无肿大9例,脾肿大率55％。淋巴结局部肿大3例,全身淋巴结肿大6例,无肿大6
Malignant cytopathic since the first report in 1957 Tian domestic field has been 20 years of history, now we from 1966 to 1977 admitted 20 cases are analyzed as follows. First, clinical data The group of 15 males and 5 females, male to female ratio of 3: 1. The youngest 1 year old, the oldest 74 years old, average 35 years old, 15 to 45 years old accounted for 75% (15/20). Occupation: 8 workers, 7 farmers, 2 cadres, 1 student, no job in 2 cases, workers and peasants accounted for 75%. Symptoms and signs: fever in 20 cases, failure in 15 cases, anemia in 14 cases, skin and mucous membrane hemorrhage in 7 cases, scleral skin yellow dye in 5 cases, skin nodules in 2 cases, gastrointestinal bleeding in 8 cases, gastrointestinal perforation in 2 cases, skin ulcer 1 example. Hepatomegaly 1.5 cm below 5 cases, 1.5 to 3 cm 8 cases, 3 to 6 cm 2 cases, no enlargement in 5 cases, hepatomegaly 75%. Splenomegaly 1.5 cm below 6 cases, 1.5 to 3 cm 3 cases, 3 to 6 cm 2 cases, 9 cases of splenomegaly, splenomegaly 55%. Local lymph nodes in 3 cases, systemic lymphadenopathy in 6 cases, no enlargement 6