【不明原因发热的罕见鉴别诊断】。

Sabrina Welland, Linus Risser, René Abu Isneineh
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引用次数: 0

摘要

22岁男性患者,临床表现与败血症相似,根据临床和实验室标准诊断为成人斯蒂尔氏病巨噬细胞激活综合征。诊断检查包括对持续性发热综合征的鉴别诊断和对噬血细胞淋巴组织细胞增多症的鉴别诊断。开始了地塞米松、免疫球蛋白和阿那白的免疫抑制治疗,并取得了持续的临床缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A rare differential diagnosis of fever of unknown origin].

A 22-year-old male patient with a clinical picture similar to that of sepsis was diagnosed with macrophage activation syndrome in adult Still's disease on the basis of clinical and laboratory criteria. The diagnostic work-up included the differentiated clarification of a persistent fever syndrome and the differential diagnosis of hemophagocytic lymphohistiocytosis. Immunosuppressive therapy with dexamethasone, immunoglobulins and anakinra was initiated and a sustained clinical remission was achieved.

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