吞噬血细胞综合征合并成人发病斯蒂尔氏病患者血清铁蛋白水平极高

G. Sargin, T. Senturk, I. Yavaşoğlu, Firuzan Kacar-Doger
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引用次数: 5

摘要

噬血细胞综合征(HS)和成人发病的斯蒂尔氏病(AOSD)都是罕见的全身性炎症性疾病。这些炎症性疾病可能很难相互区分。有一些迹象可以帮助临床医生诊断,如AOSD的高铁蛋白水平,HS的白细胞减少,血小板减少,高甘油三酯血症。成人发病斯蒂尔氏病继发的噬血细胞综合征文献报道甚少。在这篇文章中,我们的目的是报告一名65岁女性,诊断为HS和AOSD,血清铁蛋白水平极高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extremely high serum ferritin level in a patient with Hemophagocytic Syndrome and Adult-Onset Still's disease
Hemophagocytic syndrome (HS) and Adult-onset Still’s disease (AOSD) are both rarely systemic inflammatory disorders. It may be difficult to differentiate these inflammatory disorders from each other. There are some signs that may help clinicians in the diagnosis such as high ferritin levels for AOSD, and leukopenia, thrombocytopenia, hypertriglyceridemia for HS. Hemophagocytic syndrome secondary to Adult-onset Still’s disease was reported rarely in literature. In this article, we aimed to report a patient of 65-year old female diagnosed with HS and AOSD with extremely high serum ferritin levels.
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