Sclerosing mucoepidermoid carcinoma of salivary glands.

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-11-14 DOI:10.1007/s00428-024-03970-x
Bacem Khalele Othman, Martina Bradová, Roderick H W Simpson, Jan Laco, Abbas Agaimy, Miguel Rito, Stephan Ihrler, Petr Steiner, Petr Grossmann, Veronika Hájková, Gisele de Rezende, Montse Goma, Senada Koljenovic, Isabel Fonseca, Michal Michal, Ilmo Leivo, Alena Skalova
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Abstract

Sclerosing mucoepidermoid carcinoma (SMEC) of the salivary glands is a rare variant of low-grade mucoepidermoid carcinoma with scanty cellular atypia characterized by marked fibrosis/sclerosis and a rich inflammatory infiltrate. Herein, we report 25 unpublished cases of SMEC, two of them with prominent eosinophilia (2/25; 8%) and three with abundant IgG4-positive plasma cells (3/25; 12%). In our series of salivary SMEC, molecular analysis using fluorescence in situ hybridization (FISH) and/or next-generation sequencing (NGS) provided evidence of MAML2 gene rearrangement in 18 cases of the 21 analyzable cases tested (86%), while this gene locus was intact in 3 cases (14%). This study focuses on the diagnostic criteria of salivary SMEC given its challenge of abundant collagenous stroma, minimal residual neoplastic areas, and inconspicuous mucous cells. Follow-up data of our cases indicate that salivary SMECs have favorable outcomes. Molecular analysis for MAML2 gene rearrangement suggests that SMECs of salivary glands represent a rare variant of conventional low-grade MECs of salivary glands. In contrast, SMECs of the thyroid gland are genetically distinct from salivary-type thyroid MECs.

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涎腺硬化性粘液表皮样癌。
唾液腺硬化性粘液表皮样癌(SMEC)是低级别粘液表皮样癌的一种罕见变异型,细胞不典型性稀少,以明显的纤维化/硬化和丰富的炎症浸润为特征。在此,我们报告了 25 例未发表的 SMEC 病例,其中两例伴有明显的嗜酸性粒细胞增多(2/25;8%),三例伴有大量 IgG4 阳性浆细胞(3/25;12%)。在我们的唾液 SMEC 系列中,使用荧光原位杂交(FISH)和/或新一代测序(NGS)进行的分子分析为 21 例可分析病例中的 18 例(86%)提供了 MAML2 基因重排的证据,而 3 例(14%)的该基因位点完好无损。本研究的重点是唾液 SMEC 的诊断标准,因为唾液 SMEC 面临的挑战是胶原基质丰富、残留肿瘤区域极小、粘液细胞不明显。病例的随访数据表明,唾液腺 SMEC 的治疗效果良好。MAML2 基因重排的分子分析表明,唾液腺 SMECs 是传统低级别唾液腺 MECs 的一种罕见变异。相比之下,甲状腺SMECs与唾液型甲状腺MECs在基因上截然不同。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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