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Diagnosis of Follicular Lesions of Undetermined Significance in Fine-Needle Aspirations of Thyroid Nodules

机译:甲状腺结节细针穿刺的滤泡性病变的诊断价值未确定

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摘要

Aim. We aimed to analyze the diagnostic criteria proposed by the Bethesda System for Reporting Thyroid Cytopathology for follicular lesions of undetermined significance (FLUS), the risk of cancer and diagnostic improvement with use of immunocytochemistry. Methods. For each FLUS diagnosis, we analyzed the cytological criteria (9 Bethesda criteria), secondary fine-needle aspiration (FNA) results, surgical procedures, contribution of immunocytochemistry with the antibodies cytokeratin 19 (CK19) and monoclonal anti-human mesothelial cell (HBME1). Results. Among patients with 2,210 thyroid FNAs, 244 lesions (337 nodules) were classified as FLUS (11% of all thyroid FNAs). The 3 criteria most often applied were cytological atypia suggesting papillary carcinoma (36%), microfollicular architecture but sparse cellularity (23.1%), cytological atypia (21.5%). With secondary FNA, 48.8% of nodules were reclassified as benign. For about half of all cases (41.4% for the first FNA, 57.6% for the second FNA), immunocytochemistry helped establishing a diagnosis favoring malignant or benign. No benign immunocytochemistry results were associated with a malignant lesion. In all, 22.5% of the 39 removed nodules were malignant. Conclusion. The FLUS category is supported by well-described criteria. The risk of malignancy in our series was 22.5%. Because we had no false-negative immunocytochemistry results, immunocytochemistry could be helpful in FLUS management.
机译:目标。我们旨在分析Bethesda系统提出的诊断标准,该标准用于报告甲状腺细胞病理学对未定意义的滤泡性病变(FLUS),癌症风险和免疫细胞化学方法的诊断改善。方法。对于每种FLUS诊断,我们分析了细胞学标准(贝塞斯达标准9条),次要细针穿刺抽吸(FNA)结果,手术程序,细胞角蛋白19(CK19)抗体和单克隆抗人间皮细胞(HBME1)对免疫细胞化学的贡献。结果。在有2,210例甲状腺FNA的患者中,有244个病变(337个结节)被分类为FLUS(占所有甲状腺FNA的11%)。最常使用的3个标准是提示乳头状癌的细胞学非典型性(36%),微泡结构但细胞稀疏(23.1%),细胞学非典型性(21.5%)。对于继发性FNA,48.8%的结节被重新分类为良性。对于所有病例的大约一半(第一个FNA为41.4%,第二个FNA为57.6%),免疫细胞化学有助于建立有利于恶性或良性的诊断。没有良性免疫细胞化学结果与恶性病变相关。在39个切除的结节中,总共有22.5%为恶性。结论。详尽描述的标准支持FLUS类别。我们系列中的恶性肿瘤风险为22.5%。因为我们没有假阴性的免疫细胞化学结果,所以免疫细胞化学可能有助于FLUS的管理。

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