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成人Still 病伪装为急性冠状动脉综合征:病例报告及文献复习。

Adult-onset Still's disease masquerading as acute coronary syndrome: a case report and review of the literature.

机构信息

Penn State College of Medicine, Hershey, PA, USA.

Division of Rheumatology, Department of Medicine, Penn State Health Milton S. Hershey Medical Center, Hershey, PA, USA.

出版信息

J Med Case Rep. 2024 Oct 10;18(1):489. doi: 10.1186/s13256-024-04799-3.

Abstract

INTRODUCTION

Adult-onset Still's disease is a rare systemic autoinflammatory disease. We present a case of a young man with a constellation of symptoms and myopericarditis as a complication of this disease.

CASE

A 36-year-old Hispanic man with no significant past medical history developed a quotidian fever pattern following an upper respiratory tract infection. He initially presented with chest pain concerning for myocardial infarction and underwent cardiac catheterization, which revealed non-obstructive coronary artery disease. He was found to have myopericarditis, significant neutrophilic leukocytosis, and hyperferritinemia. He improved on high-dose corticosteroids but developed steroid-induced psychosis, and 4 months from symptom onset, he finally received tocilizumab, which eventually induced remission without adverse reactions.

DISCUSSION

Adult-onset Still's disease should be considered in a patient with fevers of undetermined origin. Due to its multisystemic involvement, adult-onset Still's disease is often a diagnosis arrived at after an extensive cardiac, hematologic, malignant, and infectious workup. Imaging, laboratory testing, and bone marrow biopsy were necessary to rule out alternative etiologies of this patient's presentation. Steroids are the mainstay of treatment because they are easily affordable, although the high risk of adverse effects makes them less desirable. Interleukin-1 inhibitors (anakinra or canakinumab) and interleukin-6 inhibitor tocilizumab are the steroid-sparing biologic agents of choice but are cost-prohibitive.

CONCLUSION

Adult-onset Still's disease should be considered in the differential diagnoses of fever of undetermined origin. Early identification and initiation of treatment are critical to faster recovery and prevention of progression to severe complications. Steroids remain the standard first-line therapy and should be followed by disease-modifying steroid sparing drugs. The social determinants of health may preclude their timely initiation and should alert providers of proactive ways to avoid further delays.

摘要

简介

成人斯蒂尔病是一种罕见的全身炎症性疾病。我们报告了一例年轻男性,其具有一系列症状,并发心肌炎。

病例

一名 36 岁的西班牙裔男性,既往无重大病史,在上呼吸道感染后出现每日发热模式。他最初表现为胸痛,疑似心肌梗死,并接受了心脏导管检查,结果显示非阻塞性冠状动脉疾病。他被发现患有心肌炎、显著中性粒细胞白细胞增多和铁蛋白血症升高。他接受了大剂量皮质类固醇治疗后有所改善,但出现了类固醇诱导的精神病,在症状出现 4 个月后,他最终接受了托珠单抗治疗,最终无不良反应诱导缓解。

讨论

对于原因不明的发热患者,应考虑成人斯蒂尔病。由于其多系统受累,成人斯蒂尔病通常是在广泛的心脏、血液、恶性和感染性检查后得出的诊断。为了排除该患者表现的其他病因,需要进行影像学、实验室检查和骨髓活检。皮质类固醇是主要的治疗方法,因为它们容易获得,尽管存在高不良反应风险,使其不太理想。白细胞介素-1 抑制剂(阿那白滞素或卡那白滞素)和白细胞介素-6 抑制剂托珠单抗是皮质类固醇的首选生物制剂,但价格昂贵。

结论

对于原因不明的发热,应考虑成人斯蒂尔病的鉴别诊断。早期识别和开始治疗对于更快的康复和预防严重并发症的进展至关重要。皮质类固醇仍然是标准的一线治疗方法,随后应使用疾病修饰性类固醇节省药物。健康的社会决定因素可能会妨碍其及时启动,应提醒提供者采取积极主动的方法避免进一步延误。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a533/11465706/5e4cf93391b3/13256_2024_4799_Fig1_HTML.jpg

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