Pathology, Fimlab Laboratories, Tampere, Finland.
Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Diagn Cytopathol. 2024 May;52(5):271-287. doi: 10.1002/dc.25284. Epub 2024 Feb 13.
The classification terminology systems for pulmonary cytology specimens have recently emerged. Inadequate samples, classified as "nondiagnostic," raise challenges in determining the threshold of cell numbers and the risk of malignancy (ROM).
The study retrospectively reviewed 248 endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) samples: 46 insufficient samples, 60 low cellularity samples, and 142 adequate samples. Characteristics as cellularity, number of benign and malignant cells, and background features were assessed. Receiver operating characteristic curve analysis was performed to establish cell sufficiency thresholds for the diagnosis.
Out of the 248 samples analyzed, 108 were classified as benign, 94 as malignant, and 46 as insufficient. The study found that the cellularity thresholds for diagnosis in cell blocks and cytological samples were ≥50 cells and ≥100 cells, respectively. The thresholds for tumor cell counts were ≥1 - 10 cells for both types of cells, respectively. Considerably, some low cellularity samples were initially classified as insufficient despite meeting the diagnostic thresholds upon revision. The ROM varied across sample categories, with insufficient samples having a ROM of 10.9%, benign samples 15.7%, suspicious samples 92.0%, and malignant samples 100%.
Insufficient EBUS-TBNA samples raise challenges in diagnosis and management. This study identified the root cause of insufficient samples, including factors related to humans, diagnostic methods, sampling, and laboratory processing. By understanding the root causes, diagnostic recommendations can be developed to improve the diagnostic process. The findings emphasize the importance of standardized classification and terminology systems for clear communication among healthcare professionals and institutions, ultimately improving patient care and enabling quality assurance measures.
肺部细胞学标本的分类术语系统最近已经出现。标本不足,被归类为“非诊断性”,这给确定细胞数量的阈值和恶性肿瘤风险(ROM)带来了挑战。
本研究回顾性分析了 248 例经支气管超声引导下经支气管针吸活检(EBUS-TBNA)标本:46 例标本不足,60 例细胞数量少,142 例标本充足。评估了细胞数量、良性和恶性细胞数量以及背景特征等特征。进行了接受者操作特征曲线分析,以确定诊断的细胞充足阈值。
在分析的 248 例标本中,108 例被归类为良性,94 例为恶性,46 例为不足。研究发现,细胞块和细胞学标本诊断的细胞数量阈值分别为≥50 个细胞和≥100 个细胞。肿瘤细胞计数的阈值分别为两种细胞类型的≥1-10 个细胞。值得注意的是,一些细胞数量少的标本尽管在重新评估时符合诊断阈值,但最初被归类为不足。ROM 因样本类别而异,不足样本的 ROM 为 10.9%,良性样本为 15.7%,可疑样本为 92.0%,恶性样本为 100%。
不足的 EBUS-TBNA 标本在诊断和管理方面带来了挑战。本研究确定了不足样本的根本原因,包括与人类、诊断方法、采样和实验室处理相关的因素。通过了解根本原因,可以制定诊断建议,以改善诊断过程。研究结果强调了标准化分类和术语系统对于医疗保健专业人员和机构之间清晰沟通的重要性,最终提高了患者护理水平,并实现了质量保证措施。