Siddique Rehan, Alezergawi Sally, Patel Aminah, Khan Amber
Department of Diabetes and Endocrinology, Salford Royal NHS Foundation Trust, Manchester, GBR.
Cureus. 2025 Jun 16;17(6):e86134. doi: 10.7759/cureus.86134. eCollection 2025 Jun.
Giant cell arteritis (GCA), a vasculitis of medium- and large-sized arteries, frequently manifests with symptoms such as headaches, soreness in the scalp, and vision abnormalities. Pyrexia is an uncommon symptom and can cause a delay in diagnosis. We describe a 76-year-old woman of Chinese ethnicity who did not exhibit the typical clinical signs of GCA but instead presented with a generalized lethargy, nausea, dizziness, and a persistent fever. Numerous tests, including autoimmune, neoplastic, and viral workups, came up negative. Pyrexia did not settle despite using broad-spectrum antibiotics. A temporal artery Doppler ultrasound was performed to assess the condition further, as inflammatory markers (erythrocyte sedimentation rate, ESR, and C-reactive protein) remained high. The ultrasound Doppler results showed bilateral halo signs that are very specific for GCA. Upon starting corticosteroid treatment, there was a rapid improvement in fever and ESR. This case underscores the importance of considering GCA as a differential diagnosis for pyrexia of unknown origin, particularly in the elderly. It highlights the utility of temporal artery ultrasound in facilitating timely diagnosis in atypical cases.
巨细胞动脉炎(GCA)是一种中大型动脉的血管炎,常表现为头痛、头皮酸痛和视力异常等症状。发热是一种不常见的症状,可能导致诊断延迟。我们描述了一位76岁的华裔女性,她没有表现出GCA的典型临床体征,而是出现了全身乏力、恶心、头晕和持续发热。包括自身免疫、肿瘤和病毒检查在内的多项检查结果均为阴性。尽管使用了广谱抗生素,发热仍未消退。由于炎症指标(红细胞沉降率、ESR和C反应蛋白)仍然很高,因此进行了颞动脉多普勒超声检查以进一步评估病情。超声多普勒结果显示双侧晕征,这对GCA具有高度特异性。开始使用皮质类固醇治疗后,发热和ESR迅速改善。该病例强调了将GCA作为不明原因发热的鉴别诊断的重要性,尤其是在老年人中。它突出了颞动脉超声在非典型病例中促进及时诊断的作用。