Diagnostic Performance of the Milan System for Reporting Salivary Gland Cytopathology and a Proposed Algorithm for Fine-Needle Aspiration Cytology of Salivary Gland Lesions.

IF 1.6 4区 医学 Q3 PATHOLOGY
Acta Cytologica Pub Date : 2025-04-21 DOI:10.1159/000546005
Norihide Mochizuki, Hirotaka Fujita, Takuma Tajiri, Masataka Ueda, Makiko Kurata, Chie Inomoto, Tomoko Sugiyama, Daisuke Maki, Shuichi Shiraishi, Tomohisa Machida, Hitoshi Ito, Yohei Masugi, Naoya Nakamura
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引用次数: 0

Abstract

Introduction: We evaluated concordance between Milan System for Reporting Salivary Gland Cytopathology (MSRSGC)-based categorization of salivary gland masses/lesions screened by fine-needle aspiration cytology (FNAC) and final histopathologic diagnoses, aiming to identify factors predictive of concordance, with the goal of appropriate case management.

Methods: The study was retrospective and involved 101 cases of salivary mass/lesion examined by FNAC. We compared MSRSGC categories against the final histopathologic classes (non-neoplasm, benign neoplasm, or malignant neoplasm) and calculated diagnostic concordance in each class. Concordance was defined as: MSRSGC categorization of a lesion as a category Ⅱ lesion and a histopathologic classification as a non-neoplasm; MSRSGC categorization of a lesion as a category Ⅳ-A lesion and a histopathologic classification as a benign neoplasm; or MSRSGC categorization of a lesion as a category Ⅴ or Ⅵ lesion and a histopathologic classification as a malignant neoplasm. We then compared clinicopathologic factors between concordant and discordant cases.

Results: Diagnostic concordance for non-neoplasms, benign neoplasms, malignant neoplasms, and total cases was 81.8% (9/11), 81.7% (58/71), 66.6% (8/12), and 79.8% (75/94), respectively, with no significant between-class difference. We found the shortest distance from the body surface to the salivary lesion differed significantly between the concordant group and the discordant group (5.35 mm vs. 7.30 mm), and the optimal cut-off was determined to be 8.00 mm (P < 0.01).

Conclusion: Based on the distance of either <8mm or ≧8mm from the body surface to the mass/lesion, we believe our proposed FNAC algorithm of treatment strategies is a reliable guide for otolaryngologists on evaluating salivary gland lesions.

报告唾液腺细胞病理学的米兰系统的诊断性能和唾液腺病变细针穿刺细胞学的建议算法。
简介:我们评估了通过细针穿刺细胞学(FNAC)筛选的唾液腺肿块/病变的基于米兰唾液腺细胞病理学报告系统(MSRSGC)分类与最终组织病理学诊断之间的一致性,旨在确定预测一致性的因素,以实现适当的病例管理。方法:回顾性分析101例经FNAC检查的唾液肿块/病变。我们将MSRSGC分类与最终的组织病理分类(非肿瘤、良性肿瘤或恶性肿瘤)进行比较,并计算每一类的诊断一致性。一致性定义为:MSRSGC将病变分类为Ⅱ病变类别,组织病理学分类为非肿瘤;MSRSGC将病变分类为Ⅳ-A类病变和组织病理学分类为良性肿瘤;或MSRSGC将病变分类为Ⅴ或Ⅵ类病变,并将组织病理学分类为恶性肿瘤。然后,我们比较了一致病例和不一致病例的临床病理因素。结果:非肿瘤、良性肿瘤、恶性肿瘤和总病例的诊断符合率分别为81.8%(9/11)、81.7%(58/71)、66.6%(8/12)和79.8%(75/94),两组间差异无统计学意义。我们发现,和谐组和不和谐组体表到唾液腺病变的最短距离差异显著(5.35 mm vs. 7.30 mm),最佳临界值确定为8.00 mm (P < 0.01)。结论:基于体表到肿块/病变的距离<8mm或≧8mm,我们认为我们提出的治疗策略FNAC算法是耳鼻喉科医生评估唾液腺病变的可靠指南。
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来源期刊
Acta Cytologica
Acta Cytologica 生物-病理学
CiteScore
3.70
自引率
11.10%
发文量
46
审稿时长
4-8 weeks
期刊介绍: With articles offering an excellent balance between clinical cytology and cytopathology, ''Acta Cytologica'' fosters the understanding of the pathogenetic mechanisms behind cytomorphology and thus facilitates the translation of frontline research into clinical practice. As the official journal of the International Academy of Cytology and affiliated to over 50 national cytology societies around the world, ''Acta Cytologica'' evaluates new and existing diagnostic applications of scientific advances as well as their clinical correlations. Original papers, review articles, meta-analyses, novel insights from clinical practice, and letters to the editor cover topics from diagnostic cytopathology, gynecologic and non-gynecologic cytopathology to fine needle aspiration, molecular techniques and their diagnostic applications. As the perfect reference for practical use, ''Acta Cytologica'' addresses a multidisciplinary audience practicing clinical cytopathology, cell biology, oncology, interventional radiology, otorhinolaryngology, gastroenterology, urology, pulmonology and preventive medicine.
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