4.2 Article

Long-Term Efficacy of Ultrasound-Guided Percutaneous Laser Ablation for Low-Risk Papillary Thyroid Microcarcinoma: A 5-Year Follow-Up Study

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BIOMED RESEARCH INTERNATIONAL
卷 2021, 期 -, 页码 -

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HINDAWI LTD
DOI: 10.1155/2021/6616826

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资金

  1. National Natural Science Foundation of China [81871367]
  2. Key Research and Development Program of Hunan Province, China [2018SK21217]

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Ultrasound-guided percutaneous laser ablation is a safe and effective alternative clinical treatment for low-risk papillary thyroid microcarcinoma, achieving a 100% success rate for single ablation with minimal side effects and no serious complications reported. Ablated lesions showed significant reduction in volume over time, with 100% complete absorption by 24 months post-ablation in majority of cases.
Objective. To evaluate the long-term efficacy and safety of ultrasound-guided percutaneous laser ablation (PLA) for the treatment of low-risk papillary thyroid microcarcinoma (PTMC). Methods. From June 2012 to May 2015, 105 patients with solitary, pathologically confirmed PTMC lesions were treated with ultrasound-guided PLA. Nodule location, nodule volume, thyroid function, and clinical symptoms were evaluated before ablation. Contrast-enhanced ultrasound (CEUS) was performed 1 h after treatment to evaluate whether the ablation was complete. Ultrasound examination was performed at 1, 3, 6, and 12 months after ablation and every 6 months thereafter to determine the size of the ablation area and search for recurrence in the thyroid parenchyma and lymph node metastasis. Thyroid function was examined before and 1 month after ablation. Fine needle aspiration biopsy was performed for any suspicious metastatic lymph nodes and recurrent lesions in the thyroid. Results. All 105 lesions were completely inactivated after one ablation, making the success rate for single ablation 100%. The average ablation time was 2.78 +/- 1.05 min, and the average ablation energy was 505 +/- 185 J. All patients could tolerate and complete the ablation. No serious complications occurred during the treatment; only minor side effects such as pain and local discomfort were reported. The volume reduction rates were -781.14 +/- 653.29% at 1 h posttreatment and -268.65 +/- 179.57%, -98.39 +/- 76.58%, 36.78 +/- 30.32%, 75.55 +/- 21.81%, 96.79 +/- 10.57%, and 100% at 1, 3, 6, 12, 18, and 24 months after ablation, respectively. This rate remained 100% at the later follow-up times. Overall, 28 (26.67%), 74 (70.48%), 96 (91.43%), and 103 (100%) were completely absorbed by 6, 12, 18, and 24 months after PLA. One patient developed another lesion 12 months after ablation, and two patients had central cervical lymph node metastasis 24 months after ablation. Conclusion. PLA is a safe and effective alternative clinical treatment for low-risk PTMC.

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