变应性亚败血症(Subsepsis allergica),是临床上较少见的疾病之一,国内文献报告以儿科病例多见,成人病例较少,而且其临床表现特殊,早期诊断比较困难。为加强对本病的认识,将本院1974～1980年所见的6例报告如下。临床资料一、一般资料:本组6例中,男性2例,女性4例;年龄最小15岁,最大36岁。二、诊断依据:本病缺乏特异性诊断方法,主要是根据典型的临床表现及排除其他类似疾病而诊断的[1、2],主要为:1.长期反复发作间歇性弛张热,发热时伴一过性皮疹,虽有长期间歇性高热,但一般状况尚好。2.有明显的白细胞数增多,中性核左移,血沉加速,血培养阴性。3.高热时用一般退热剂及抗菌素治疗无效,用肾上腺皮质激素类药物治疗有明显的疗 Subsepsis allergica is one of the less clinically rare diseases. The domestic literature reports are more common in pediatric cases, fewer adult cases, and its clinical manifestations are rather difficult to diagnose early. In order to strengthen the understanding of this disease, we report 6 cases seen in our hospital from 1974 to 1980 as follows. Clinical data First, the general information: The group of 6 patients, 2 males and 4 females; the youngest 15 years old, maximum 36 years old. Second, the diagnosis is based on: the lack of specific diagnosis of the disease, mainly based on the typical clinical manifestations and exclude other similar diseases and diagnosed [1,2], mainly as follows: 1. Long-term recurrent intermittent fever, fever With a transient rash, although long-term intermittent fever, but the general condition is still good. 2. There is a clear increase in the number of white blood cells, left shift of the neutral nucleus, erythrocyte sedimentation rate, blood culture negative. 3. High fever with antipyretics and antipyretics generally ineffective treatment with adrenal cortex hormones obvious treatment