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首页> 外文期刊>Pediatric emergency care >Simultaneous Acquired Self-limited Hemophagocytic Lymphohistiocytosis and Kikuchi Necrotizing Lymphadenitis in a 16-Year-Old Teenage Girl A Case Report and Review of the Literature
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Simultaneous Acquired Self-limited Hemophagocytic Lymphohistiocytosis and Kikuchi Necrotizing Lymphadenitis in a 16-Year-Old Teenage Girl A Case Report and Review of the Literature

机译:16岁少女同时获得性自限性噬血细胞淋巴组织增多和菊池坏死性淋巴结炎的病例报告及文献复习

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Objectives: The aim of this study was to increase education and awareness among pediatric practitioners of possibility of simultaneous hemophagocytic lymphohistiocytosis and Kikuchi-Fujimoto disease/Kikuchi disease occurring in the pediatric population and the diagnostic dilemma it can present. We describe a case presentation of acquired and self-limited simultaneous hemophagocytic lymphohistiocytosis and Kikuchi-Fujimoto disease in a 16-year-old in the United States who presented with fevers, night sweats, and joint pain, along with tiredness and decreased appetite along with pancytopenia and elevated lactate dehydrogenase. To the best of our knowledge, simultaneous hemophagocytic lymphohistiocytosis and Kikuchi-Fujimoto in the pediatric population has not been described in North America but remains fairly common in Asia. The literature on both diseases and their simultaneous occurrence is comprehensively reviewed.
机译:目的:本研究的目的是提高小儿科医师对小儿人群同时发生吞噬性淋巴细胞组织细胞增多症和菊池藤本病/菊池病的可能性及其诊断难题的教育和认识。我们描述了在美国16岁时出现发烧,盗汗,关节痛,疲倦和食欲不振以及获得性和自限性同时吞噬性淋巴细胞性组织细胞增多症和菊池藤本病的病例报告全血细胞减少症和乳酸脱氢酶升高。据我们所知,在北美,尚未发现儿科人群同时发生吞噬性淋巴细胞组织细胞增生和菊池藤本,但在亚洲仍然相当普遍。对这两种疾病及其同时发生的文献进行了全面回顾。

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