伴有牙痛的巨细胞动脉炎

IF 1.8 Q2 MEDICINE, GENERAL & INTERNAL Journal of General and Family Medicine Pub Date : 2024-03-13 DOI:10.1002/jgf2.684
Jun Usami MD, PhD
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引用次数: 0

摘要

一名 78 岁的妇女因不明原因的低烧 4 周前来门诊就诊。发烧一周后,她因左上牙痛和左下颌跛行到牙科诊所就诊,并被安排制作口模。没有发现龋齿。由于发烧原因不明,患者来到我们诊所就诊。就诊时,她神志清醒,生命体征正常。体格检查显示左侧颞动脉轻度肿大,无搏动和压痛(图 1A)。她没有抱怨肩部、颈部、髋腰部和大腿近端疼痛和晨僵。她没有多发性风湿痛的并发症。她的 C 反应蛋白水平为 4.8 毫克/分升(参考值:0-0.3 毫克/分升),红细胞沉降率为 85 毫米/小时(参考值:0-10 毫米/小时)。超声波检查显示两侧颞动脉额支管壁增厚(图1B;左侧颞动脉)。左颞动脉活检显示管腔高度狭窄。在血管壁上观察到淋巴细胞、中性粒细胞浸润和肉芽组织形成,还观察到多核巨细胞。活组织检查结果证实了诊断,每天口服 40 毫克泼尼松龙(1 毫克/千克体重)1。在一份报告中,超过 80% 的病例出现头痛。2 我们的患者主诉牙痛,但她的牙齿没有任何问题。巨细胞动脉炎也可能导致失明等严重危害3 ,因此需要及时诊断。巨细胞动脉炎在日本、韩国和其他亚洲国家的发病率低于西方国家,造成这种差异的原因尚不清楚。在亚洲国家,GCA 是不明原因发热的原因之一。在初级医疗机构中,对于发热和太阳穴疼痛的亚洲老年患者,应考虑 GCA 的可能性;应进行超声波检查,以检测颞动脉额支管壁是否增厚。这种简便的方法对于诊断这种急诊疾病非常有用。没有报告与本文相关的潜在利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Giant-cell arteritis with toothache

A 78-year-old woman visited the outpatient clinic with a 4-week history of low-grade fever of unknown origin. One week after fever onset, she visited the dental clinic because of upper left toothache and left jaw claudication, and she was scheduled to have a mouthpiece made. No dental caries was observed. Since the cause of fever was not clear, the patient visited our clinic. On presentation, she was alert, and her vital signs were normal. Physical examination revealed a slightly enlarged left temporal artery without pulsation and tenderness (Figure 1A). She did not complain of pain and morning stiffness about the shoulders, neck, hip girdle, and proximal thighs. There were no complications of polymyalgia rheumatica. Her C-reactive protein level was 4.8 mg/dL (reference: 0–0.3 mg/dL), and erythrocyte sedimentation rate was 85 mm/h (reference: 0–10 mm/h). Ultrasonography revealed thickened walls in both the temporal artery frontal branches (Figure 1B; left temporal artery). Giant-cell arteritis (GCA) was considered likely.1 Left temporal artery biopsy was performed, which revealed a highly narrowed lumen. Lymphocytes, neutrophil infiltration, and granulation tissue formation were observed in the blood vessel wall, and multinucleated giant cells were also observed. The biopsy results confirmed the diagnosis, and 40 mg prednisolone (1 mg/kg body weight) was orally administered daily.1 Symptoms resolved within a week.

Giant-cell arteritis is a vasculitis that often affects medium- and large-sized arteries and shows a variety of clinical manifestations (Table 1). Headache is present in over 80% of cases in a report.2 Our patient complained of toothache, but she had no problems with her teeth. Giant-cell arteritis can also cause serious risks, such as blindness,3 and requires prompt diagnosis. Giant-cell arteritis occurs less often in Japan, Korea, and other Asian countries than in Western countries; the reason for this discrepancy remains unclear. In Asian countries, GCA is one of the cause of fever of unknown origin. In primary care settings, the possibility of GCA should be considered in elderly Asian patients suffering from fever and pain in the temple; ultrasonography should be performed to detect wall thickening in the temporal artery frontal branches. This easy method is very useful for the diagnosis of this emergent disease.

None.

No potential conflict of interest relevant to this article was reported.

None.

We obtained informed consent from the patient for this case report.

None.

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来源期刊
Journal of General and Family Medicine
Journal of General and Family Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
2.10
自引率
6.20%
发文量
79
审稿时长
48 weeks
期刊最新文献
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