Ultrasonographic findings as diagnostic and follow-up tool in cranial giant cell arteritis
Ultrasonographic findings as diagnostic and follow-up tool in cranial giant cell arteritis
复制标题
超声检查结果作为颅巨细胞动脉炎的诊断和随访工具
DOI:
10.1093/qjmed/hcx174
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发表时间:
2017
期刊:
影响因子:
--
通讯作者:
Terada Y
中科院分区:
文献类型:
--
作者:
Taniguchi Y;Nishikawa H;Amano E;Fujimoto S;Terada Y
A 79-year-old man presented with a three-week history of fever, rapidly progressive declining visual acuity, and jaw claudication. The biochemical profile showed elevated levels of C-reactive protein (CRP)(120 mg/L; normal< 3) and an erythrocyte sedimentation rate (ESR)(140 mm/hour; normal< 10); results of testing for antineutrophil cytoplasmic antibodies and antinuclear antibody were negative. Blood cultures were negative. Hepatic and renal functions were normal. Physical examination showed palpable and funicular bilateral temporal arteries (Figure 1A, arrows). Longitudinal view of bilateral temporal arteries color Doppler ultrasonography (US) features before treatment showed a hypoechogenic halo of the temporal artery and the presence of turbulent flow and weak flow because of the presence of halo sign corresponding to edema of arterial wall (Figure 1B). Then, the biopsy of the left temporal artery demonstrated significant temporal arteritis with giant cells. The patient was diagnosed with cranial giant cell arteritis (GCA). Treatment with prednisolone was initiated. After treatment, his all symptoms resolved and ESR and serum CRP levels became normal. His abnormal physical finding of palpable and funicular bilateral temporal artery also improved (Figure 1C). Similarly, longitudinal view of temporal artery color Doppler US after treatment showed reduction of halo sign and turbulent flow and a stronger flow than before treatment that corresponds to a significant reduction of edema of artery wall (Figure 1D). Recently, the clinical implications of high-resolution magnetic resonance imaging, 1 Positron Emission Tomography and Computed Tomography Angiography2 and color Doppler ultrasonography3 have reported on diagnosis of GCA. In the present case, color Doppler US is not only very useful in the diagnosis of cranial GCA but also useful in following up of patients after initiation of therapy. This case should remind readers to consider the assessment by color Doppler US as convenient monitoring tool of disease activity in cranial GCA.