细针穿刺细胞学检查在可手术乳腺癌的新辅助化疗中有重要作用。

ISRN oncology Pub Date : 2013-07-10 Print Date: 2013-01-01 DOI:10.1155/2013/935796
Christian Garbar, Hervé Curé
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引用次数: 20

摘要

尽管在无临床或影像学肿块的不可触及病变或微钙化的调查中,CNB已逐渐被FNAC所取代,但只要FNAC与三重诊断和经验丰富的细胞学家相关,FNAC在可触及病变中仍有作用。在这些情况下,FNAC是一种安全、有效、经济、准确的乳腺癌评估技术。大量文献综述和荟萃分析说明了CNB和FNAC两种方法的优缺点。当排除非信息性和不满意的FNAC时,差异似乎不显著。近年来,采用液体细胞学(LBC)技术的细胞学方法提高了免疫细胞学和分子检测的效率,与经典的免疫组织化学方法相同。FNAC的适应症为:可触及病变、CNB的相对禁忌症(老年或虚弱)、合并或不合并CNB的多发结节分期、淋巴结状态分期、新辅助治疗下患者新出现病变、快速诊断减少焦虑、生物标志物和新生物标志物的评估、新辅助治疗反应后生物标志物的时间顺序评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fine-needle aspiration cytology can play a role in neoadjuvant chemotherapy in operable breast cancer.

Fine-needle aspiration cytology can play a role in neoadjuvant chemotherapy in operable breast cancer.

Fine-needle aspiration cytology can play a role in neoadjuvant chemotherapy in operable breast cancer.

Despite the fact that CNB has been progressively replaced by FNAC in the investigation of nonpalpable lesions or microcalcifications without a clinical or radiological mass lesion, FNAC has yet a role in palpable lesions provided it is associated with the triple diagnosis and experienced cytologist. In these conditions, FNAC is a safe, effective, economical, and accurate technique for breast cancer evaluation. Numerous literature reviews and meta-analyses illustrated the advantages and disadvantages of both methods CNB and FNAC. The difference does not seem significant when noninformative and unsatisfactory FNAC was excluded. Recently, cytological methods using liquid-based cytology (LBC) technology improve immunocytological and molecular tests with the same efficiency as classical immunohistochemistry. The indications of FNAC were, for palpable lesions, relative contraindication of CNB (elderly or frailty), staging of multiple nodules in conjunction or not with CNB, staging of lymph node status, newly appearing lesion in patient under neoadjuvant treatment, decreasing of anxiety with a rapid diagnosis, evaluation of biomarkers and new biomarkers, and chronological evaluation of biomarker following the neoadjuvant therapy response.

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