摘要
The cause of hypereosinophilia (EO) in hemodialysis (HD) patients is multifactorial and is felt to be a benign laboratory abnormality related to dialysis or uremia. Kimura disease (KD) is an angiolymphoid proliferative disorder of unknown etiology. Many cases are associated with nephrotic syndrome in children; however, it has seldom been reported in children on dialysis. We report here a 13-year-old boy who developed persistent EO and subsequent anemia after maintenance HD; he later developed KD. The atypical clinical manifestation of KD and its relationship to HD and erythropoietin hyposensitive anemia in this patient are discussed.
原文 | 英語 |
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頁(從 - 到) | 183-185 |
頁數 | 3 |
期刊 | Pediatric Nephrology |
卷 | 15 |
發行號 | 3-4 |
DOIs | |
出版狀態 | 已出版 - 2000 |
對外發佈 | 是 |