一例酷似血清阴性类风湿关节炎的特发性嗜酸性粒细胞增多综合征：20年临床及实验室检查随访
An idiopathic hypereosinophilic syndrome mimicking seronegative rheumatoid arthritis: 20-year follow-up with clinical and laboratory findings.
作者信息
Prattichizzo F A, Bernini L
机构信息
Department of Internal Medicine, Hospital of San Miniato, Pisa, Italy.
出版信息
Clin Exp Rheumatol. 1992 Jan-Feb;10(1):79-81.
PMID:1551284
Abstract
A clinical case of idiopathic hypereosinophilic syndrome mimicking seronegative rheumatoid arthritis with a twenty year follow-up is reported. The patient showed other sign of the disease, such as pericarditis, gastroenteritis and hepatomegaly. Among the laboratory findings the elevated levels of aldolase and LDH 2, never reported previously, are stressed.
摘要
报告了一例疑似血清阴性类风湿关节炎的特发性嗜酸性粒细胞增多综合征临床病例，并进行了20年随访。该患者还表现出该疾病的其他体征，如心包炎、肠胃炎和肝肿大。在实验室检查结果中，强调了醛缩酶和乳酸脱氢酶2水平升高，这在以前从未有过报道。
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