Kimura病、血管淋巴样增生伴嗜酸性粒细胞增多症和肾损伤发生于同一病例

目的:报道1例少见的同时合并Kimura病和血管淋巴样增生伴嗜酸性粒细胞增多症(ALHE)的患者,并有微小病变性肾小球病导致的肾病综合征;对相关文献进行回顾总结.方法:对患者的活检标本进行组织学、免疫组织化学、免疫荧光以及电镜检查.结果:患者为37岁男性,5年来反复发作皮疹、皮肤结节、颈部淋巴结无痛性肿大和肾病综合征,经病理检查证实,肿大的淋巴结为Kimura病,皮下结节为ALHE,肾病变为微小病变性肾小球病.结论:imura病和ALHE可能是同一种疾病的不同病理表现,并可合并肾小球疾病.

One patient with Kimuraos disease and angiolymphoid hyperplasia with eosinophilia also suffers from kidney injury.]

OBJECTIVE:Reporting a rare case with Kimura's disease and angiolymphoid hyperplasia with eosinophilia (ALHE), who also has nephrotic syndrome resulting from minimal change glomerulopathy. METHODS: Histological manifestations, immunohistochemical staining, immunofluorescence staining, and electron microscope were performed. RESULTS: One 37-year-old male patient with recurrent erythra, cutaneous node, painless cervical lymph node enlargement and nephrotic syndrome in 5 years. It's confirmed through biopsies that the subcutaneous node is ALHE, the cervical lymph node is kimura disease, and renal lesion is minimal change glomerulopathy. CONCLUSION: Kimura disease and ALHE may be different features of the same disease, and may complicate glomerulopathy.