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EU-TIRADS5 甲状腺结节主动监测的结果。

Outcomes of active surveillance of EU-TIRADS 5 thyroid nodules.

机构信息

Hôpital Universitaire Pitié Salpêtrière, Thyroid and Endocrine Tumors Unit, Institute of Endocrinology, Paris, Île-de-France, France.

Centre de Pathologie et d'Imagerie, Paris, France.

出版信息

Eur J Endocrinol. 2021 May;184(5):677-686. doi: 10.1530/EJE-20-1481.

Abstract

OBJECTIVE

Active surveillance of cytologically proven microcarcinomas has been shown as a safe procedure. However, fine needle aspiration biopsy (FNAB) is not recommended by European Thyroid Association (ETA) and American Thyroid Association (ATA) guidelines for highly suspicious nodules ≤ 10 mm. The aim of the study was to assess the outcomes of active surveillance of EU-TIRADS 5 nodules ≤ 10 mm not initially submitted to FNAB.

PATIENTS AND METHODS

80 patients with at least one EU-TIRADS 5 nodule ≤ 10 mm and no suspicious lymph nodes, accepting active surveillance, were included.

RESULTS

Mean baseline diameter and volume were 5.4 mm (±2.0) and 64.4 mm3 (±33.5), respectively. After a median follow-up of 36.1 months, a volumetric increase ≥ 50% occurred in 28 patients (35.0%) and a suspicious lymph node in 3 patients (3.8%). Twenty-four patients underwent an FNAB (30.0%) after at least a 1 year follow-up of which 45.8% were malignant, 8.3% benign, 33.3% undetermined and 8.3% nondiagnostic. Sixteen patients (20.0%) underwent conversion surgery after a median follow-up of 57.2 months, confirming the diagnosis of papillary carcinoma in 15/16 cases (not described in 1 histology report), all in remission at 6-12 months postoperative follow-up.

CONCLUSION

Applying ETA and ATA guidelines to avoid FNA of EU-TIRADS 5 sub-centimeter nodules and proceeding to active surveillance of such nodules in selected patients is a safe procedure. Thus, US-FNAB could be postponed until the nodule shows signs of progression or a suspicious lymph node appears, with no added risk for the patient.

摘要

目的

细胞学证实的微癌的主动监测已被证明是一种安全的方法。然而,欧洲甲状腺协会(ETA)和美国甲状腺协会(ATA)指南不建议对高度可疑的≤10mm 的结节进行细针抽吸活检(FNAB)。本研究的目的是评估未行 FNAB 的≤10mm 的高度可疑的 EU-TIRADS 5 结节的主动监测的结果。

患者和方法

共纳入 80 例至少有一个 EU-TIRADS 5 结节≤10mm 且无可疑淋巴结、接受主动监测的患者。

结果

平均基线直径和体积分别为 5.4mm(±2.0)和 64.4mm3(±33.5)。中位随访 36.1 个月后,28 例(35.0%)患者的体积增加≥50%,3 例(3.8%)患者出现可疑淋巴结。24 例患者在至少 1 年的随访后接受了 FNAB(30.0%),其中 45.8%为恶性,8.3%为良性,33.3%为不确定,8.3%为无法诊断。16 例(20.0%)患者在中位随访 57.2 个月后改行转换手术,15/16 例(1 例组织学报告未描述)证实为甲状腺乳头状癌,所有患者在术后 6-12 个月随访时均处于缓解期。

结论

根据 ETA 和 ATA 指南避免对 EU-TIRADS 5 亚厘米结节进行 FNAB,并对选定患者的此类结节进行主动监测是一种安全的方法。因此,US-FNAB 可以推迟到结节出现进展迹象或出现可疑淋巴结时进行,不会给患者带来额外的风险。

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