Friedman S J
William Beaumont Army Medical Center, Department of Internal Medicine, El Paso, Texas 79920-5001.
Ann Allergy. 1987 Dec;59(6):415-6.
A 16-year old boy with a 10-year history of circulating eosinophilia was diagnosed having the hypereosinophilic syndrome (HES) based upon the exclusion of other disorders. Eight years after the onset of his condition, he had a subcutaneous staphylococcal abscess followed by lymphangitis, rare clinical features of HES. As measured by radioallergosorbent techniques, there were significantly high serum levels of IgE antibodies to Staphylococcus aureus. The clinical significance of these antibodies is unknown, but their production may be due to persistent antigenic stimulation.
一名有10年循环性嗜酸性粒细胞增多病史的16岁男孩，在排除其他疾病后被诊断为高嗜酸性粒细胞综合征（HES）。在其病情发作8年后，他出现了皮下葡萄球菌脓肿，随后发生淋巴管炎，这是HES罕见的临床特征。通过放射变应原吸附技术检测，血清中抗金黄色葡萄球菌IgE抗体水平显著升高。这些抗体的临床意义尚不清楚，但其产生可能是由于持续的抗原刺激。
