作者通过常规组织学检查和纤维蛋白、免疫球蛋白、补体的免疫过氧化酶染色,以寻找Sweet综合征皮肤血管炎和免疫复合物沉积的证据.共检查15例患者(女12例,男3例),一些病例出现嗜中性白细胞增高、皮疹、关节痛和结合膜炎等典型症状.其中1例同时有B细胞淋巴瘤,随后发生系膜毛细血管性肾小球肾炎,1例发生急性胰腺炎,1例一年后发生急性髓性白血病,另1例妊娠16周. The authors sought routine evidence of evidence of Sweet’s syndrome of vasculitis and immune complex deposition by routine histological examination and immunoperoxidase staining of fibrin, immunoglobulin, and complement, and a total of 15 patients (12 females, 3 males In some cases, typical symptoms such as neutrophilia, skin rashes, arthralgia and conjunctivitis were observed in 1 case, with B-cell lymphoma followed by mesangial capillary glomerulonephritis and 1 case with acute Pancreatitis, one case of acute myeloid leukemia one year later, another case of 16 weeks of pregnancy.