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首页> 外文期刊>Ultrasound in Medicine and Biology >US-guided percutaneous radiofrequency thermal ablation for the treatment of solid benign hyperfunctioning or compressive thyroid nodules.
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US-guided percutaneous radiofrequency thermal ablation for the treatment of solid benign hyperfunctioning or compressive thyroid nodules.

机译:美国引导的经皮射频热消融术,用于治疗固体良性机能亢进或压缩性甲状腺结节。

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The aim of the study was to define the effectiveness and safety of ultrasound-guided percutaneous radiofrequency (RF) thermal ablation in the treatment of compressive solid benign thyroid nodules. Thirty-one patients not eligible for surgery or radioiodine (131I) treatment underwent RF ablation for benign nodules; a total of 33 nodules were treated (2 patients had 2 nodules treated in the same session): 10 cold nodules and 23 hyperfunctioning. Fourteen patients complained of compressive symptoms. Nodule volume, thyroid function and compressive symptoms were evaluated before treatment and at 1, 3 and 6 mo. Ultrasound-guided RF ablation was performed using a Starbust RITA needle, with nine expandable prongs; total exposure time was 6 to 10 min at 95 degrees C in one area or more of the nodule. Baseline volume (measured at the time of RF ablation) was 27.7 +/- 21.5 mL (mean +/- SD), but significantly decreased during follow-up: 19.2 +/- 16.2 at 1 mo (-32.7%; p < 0.001), 15.9 +/- 14.1 mL at 3 mo (-46.4 %; p < 0.001) and 14.6 +/- 12.6 mL at 6 mo (-50.7%; p < 0.001). After treatment, all patients with cold nodules remained euthyroid: five patients with hot nodules normalized thyroid function, and the remaining sixteen showed a partial remission of hyperthyroidism. Besides a sensation of heat and mild swelling of the neck, no major complications were observed. Improvement in compressive symptoms was reported by 13 patients, with a reduction on severity scale from 6.1 +/- 1.4 to 2.2 +/- 1.9 (p < 0.0001). Radiofrequency was effective and safe in reducing volume by about 50% and compressive symptoms in large benign nodules. Hyperfunction was fully controlled in 24% of patients and partially reduced in the others.
机译:这项研究的目的是确定超声引导下经皮射频(RF)热消融治疗压缩性甲状腺良性结节的有效性和安全性。不适合手术或放射碘治疗(131I)的31例患者因良性结节接受了射频消融;总共治疗了33个结节(2例患者在同一疗程中治疗了2个结节):10个冷结节和23个功能亢进。 14名患者主诉压迫症状。在治疗前以及1、3和6个月时评估结节体积,甲状腺功能和压迫症状。超声引导下的射频消融是使用Starbust RITA针头进行的,针头有9个可扩展的尖头。在一个或多个结节区域中,在95摄氏度下的总暴露时间为6至10分钟。基线体积(在射频消融时测量)为27.7 +/- 21.5 mL(平均+/- SD),但在随访过程中显着降低:1个月时为19.2 +/- 16.2(-32.7%; p <0.001) ),3 mo(-16.4 +/- 14.1 mL)(-46.4%; p <0.001)和6 mo(14.6 +/- 12.6 mL)(-50.7%; p <0.001)。治疗后,所有冷结节患者均保持甲状腺功能正常:5例热结节患者甲状腺功能恢复正常,其余16例显示甲状腺功能亢进症部分缓解。除了感觉发热和颈部轻度肿胀外,未观察到重大并发症。据报道有13例患者的压迫症状有所改善,严重程度评分从6.1 +/- 1.4降低至2.2 +/- 1.9(p <0.0001)。射频可有效且安全地减少大块良性结节的体积和约50%的压缩症状。功能亢进在24%的患者中得到完全控制,而在其他患者中则部分减轻。

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