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变应性亚败血症(Subsepsis allegica)是一种临床少见的综合征。本病主要表现为长期发热,一过性皮疹,关节疼痛,淋巴肿大,白细胞总数及中性粒细胞比例增高等。临床酷似败血症,同时与风湿热、淋巴瘤、结缔组织疾病亦难予鉴别,是长期发热病例诊治中应注意的一个问题。近年来国内报告的病例渐多,但成年病例较少。现将我们所见成年病人三例报告如下,并复习国内文献加以讨论。
Subsepsis allegica is a clinically uncommon syndrome. The disease mainly for long-term fever, transient rash, joint pain, lymph nodes, the total number of leukocytes and neutrophils increased. Clinical resembles sepsis, at the same time and rheumatic fever, lymphoma, connective tissue disease is difficult to identify, diagnosis and treatment of long-term fever cases should pay attention to a problem. In recent years, there have been more cases of domestic reports, but fewer adult cases. We now report three cases of adult patients reported below, and review the domestic literature to be discussed.