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巨细胞动脉炎和风湿性多肌痛患者血沉、C反应蛋白及血小板计数正常:诊断难题

Normal ESR, CRP and Platelet Count in Giant Cell Arteritis and Polymyalgia Rheumatica: A Diagnostic Conundrum.

作者信息

Mahgoub Abdullahi Elsheikh, Tessema Sophia, Nakhleh Rasha

机构信息

Department of Internal Medicine, Michigan State University at Hurley Medical Center, Flint, MI, USA.

Department of Neurology, Wayne State University, Detroit, MI, USA.

出版信息

Eur J Case Rep Intern Med. 2022 Feb 21;9(2):003192. doi: 10.12890/2022_003192. eCollection 2022.

Abstract

UNLABELLED

Giant cell arteritis (GCA) and polymyalgia rheumatica (PMR) are both rheumatological diseases of the elderly with a strong association with each other and which rarely present with normal inflammatory markers. Here we present the case of a 61-year-old Caucasian woman who had typical symptoms of both diseases. At the time of presentation, her blood work showed normal inflammatory markers, but because of the high clinical suspicion for GCA, a temporal artery biopsy was done which was positive for giant cells and disruption of the internal elastic lamina. Our patient responded very well to treatment with oral steroids and steroid-sparing medication and was able to return to her normal life without experiencing any complications of the disease. By sharing our case, we aim to increase the awareness of medical personnel regarding the importance of focusing on the clinical presentation as well as the laboratory and pathological aspects of diagnosing GCA and PMR.

LEARNING POINTS

Normal levels of inflammatory markers like C-reactive protein and the erythrocyte sedimentation rate do not rule out the diagnosis of giant cell arteritis (GCA).We aim to increase clinician recognition and awareness of other parameters, particularly the clinical presentation, that should be considered when diagnosing GCA or polymyalgia rheumatica.If the index of suspicion for the disease is high, it is crucial to start treatment as early as possible for better management and to avoid harmful complications.

摘要

未标注

巨细胞动脉炎(GCA)和风湿性多肌痛(PMR)均为老年人的风湿性疾病,二者联系紧密,且炎症指标很少正常。在此,我们报告一例61岁的白人女性病例,其具有这两种疾病的典型症状。就诊时,她的血液检查显示炎症指标正常,但由于临床高度怀疑GCA,遂进行了颞动脉活检,结果显示巨细胞阳性且内弹力层破坏。我们的患者对口服类固醇和类固醇节省药物治疗反应良好,能够恢复正常生活且未出现该疾病的任何并发症。通过分享我们的病例,我们旨在提高医务人员对关注GCA和PMR诊断的临床表现以及实验室和病理方面重要性的认识。

学习要点

C反应蛋白和红细胞沉降率等炎症指标正常并不能排除巨细胞动脉炎(GCA)的诊断。我们旨在提高临床医生对诊断GCA或风湿性多肌痛时应考虑的其他参数,特别是临床表现的认识和意识。如果对该疾病的怀疑指数较高,尽早开始治疗对于更好的管理和避免有害并发症至关重要。

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