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变应性亚败血症(以下简称亚败)系一临床综合征,又称Wissler—Fanconi综合征。临床上以发热、皮疹、关节痛、血沉增快、血白细胞增多,血培养阴性为主要特征。近十多年来国内报道日见增多。我院于1975—1985年10月间所见7例,现报告如下: 临床资料 一、发病情况:本组男性3例,女性4例。发病年龄18—55岁。病程最长1年9个月,最短1个月,平均8个月。皆无该病之家族史,无外伤史,发病前无明显的感染症状及代谢紊乱。
Allergic sepsis (hereinafter referred to as failure) is a clinical syndrome, also known as Wissler-Fanconi syndrome. Clinically, fever, rash, joint pain, ESR, leukocytosis, blood culture negative as the main feature. Over the past decade or so domestic reports have increased. Our hospital in 1975-1985 in October between the seven cases, are as follows: Clinical data First, the incidence: the group of 3 males and 4 females. Age of onset 18-55 years old. The longest duration of 1 year and 9 months, the shortest 1 month, an average of 8 months. None of the family history of the disease, no history of trauma, no obvious symptoms and metabolic disorders before onset.