Freiberger Sandra N, Ikenberg Kristian, van Egmond Demi, Claerhout Sofie, van Wezel Tom, Bempt Isabelle Vanden, van Rossem Jeroen N, Mueller Simon A, Clement Paul M, Poorten Vincent Vander, Cohen Danielle, Hauben Esther, Rupp Niels J
Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
Department of Pathology, Leiden University Medical Center, Leiden, Netherlands.
Cancer Cytopathol. 2024 Jul;132(7):435-446. doi: 10.1002/cncy.22814. Epub 2024 Apr 2.
Diagnosis of salivary gland neoplasms is challenging, especially on cytological specimens acquired by fine-needle aspiration. The recently implemented standardized Milan system for reporting salivary gland cytopathology provides an estimated risk of malignancy (ROM); yet, for two of the categories, the diagnosis of the lesion remains unclear. However, a precise diagnosis is desirable for optimal patient management, including planning of surgery and imaging procedures.
Cytological specimens (n = 106) were subjected to molecular analysis using the SalvGlandDx panel. The risk of malignancy was calculated for each detected alteration based on the diagnosis of the resection specimen. By taking into account the molecular alterations, their associated ROM, the clinical and cytological features, and the current literature, the Milan category was evaluated.
Of n = 63 technically valid cases, 76% revealed a molecular alteration. A total of 94% of these molecularly altered cases could be assigned to a different Milan category when additionally taking molecular results into account. In only 2% of the salivary gland neoplasms of uncertain malignant potential, in which a molecular alteration was detected, the classification remained salivary gland neoplasms of uncertain malignant potential.
Molecular analysis of cytological specimens provides a benefit in classifying salivary gland neoplasms on fine-needle aspiration. It can improve the ROM estimation and thus help to assign cases of formerly unknown malignant potential to clearly benign or malignant categories.
涎腺肿瘤的诊断具有挑战性,尤其是对于通过细针穿刺获取的细胞学标本。最近实施的涎腺细胞病理学标准化米兰系统提供了恶性风险估计值(ROM);然而,对于其中两个类别,病变的诊断仍不明确。然而,为了实现最佳的患者管理,包括手术和影像学检查的规划,精确的诊断是必要的。
使用SalvGlandDx检测板对106例细胞学标本进行分子分析。根据切除标本的诊断结果,计算每种检测到的改变的恶性风险。综合考虑分子改变、其相关的ROM、临床和细胞学特征以及当前文献,对米兰类别进行评估。
在63例技术上有效的病例中,76%显示存在分子改变。在综合考虑分子结果后,这些发生分子改变的病例中,共有94%可归为不同的米兰类别。在仅2%检测到分子改变的具有不确定恶性潜能的涎腺肿瘤中,分类仍为具有不确定恶性潜能的涎腺肿瘤。
对细胞学标本进行分子分析有助于对细针穿刺获取的涎腺肿瘤进行分类。它可以改善ROM估计,从而有助于将以前具有未知恶性潜能的病例归为明确的良性或恶性类别。