Atypical and worrisome histological features in pleomorphic adenoma: challenging and potentially significant diagnostic pitfall.

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2025-01-18 DOI:10.1007/s00428-024-04015-z
Reydson Alcides de Lima-Souza, Klára Bělohlávková, Michal Michal, Albina Altemani, Fernanda Viviane Mariano, Alena Skálová
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Abstract

Pleomorphic adenoma (PA), the most prevalent salivary gland tumor, exhibits a diverse histological spectrum characterized by epithelial, myoepithelial, and mesenchymal patterns, and secretory products. However, a subset of PAs presents microscopic features suggestive of malignancy, leading to challenging and potentially significant diagnostic pitfalls. A comprehensive retrospective analysis was conducted on the Salivary Gland Tumor Registry, compiled by the authors. A total of 104 cases diagnosed between 1960 and 2023 were retrieved. Clinical findings, pathological features, and molecular genetic results were analyzed. In the study of 104 PA cases, 23 (22.1%) presented features suggestive of pseudoinvasion, with satellite nodules being the most common (43.5%) along with capsular penetration, irregular growth, pseudopodia, lipomatous changes, and vascular permeation. Features of pseudomalignant cytomorphology were found in 97 cases (93.3%), characterized by increased cellularity, cellular atypia, heightened proliferative activity, oncocytic metaplasia, and necrosis. Additionally, 30 cases (28.8%) displayed features resembling other defined malignant salivary gland tumors, particularly myoepithelial carcinoma, adenoid cystic carcinoma, and polymorphous adenocarcinoma. Despite PA's generally straightforward diagnosis, cases with these features may be mistakenly interpreted as malignant tumors. The shared morphocytological features underscore the complexity of an accurate diagnosis, emphasizing the need for meticulous examination and a comprehensive assessment, incorporating morphological, molecular, and immunohistochemical analyses to differentiate between benign and malignant salivary gland tumors, in selected cases.

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多形性腺瘤的不典型和令人担忧的组织学特征:具有挑战性和潜在的重要诊断缺陷。
多形性腺瘤(PA)是最常见的唾液腺肿瘤,具有多种组织学特征,包括上皮、肌上皮和间充质模式以及分泌产物。然而,PAs的一个子集呈现出暗示恶性肿瘤的显微镜特征,导致具有挑战性和潜在的重大诊断缺陷。对作者编制的唾液腺肿瘤登记处进行了全面的回顾性分析。共检索了1960年至2023年间诊断的104例病例。分析临床表现、病理特征及分子遗传学结果。在104例PA病例的研究中,23例(22.1%)表现出假性侵犯的特征,其中卫星结节最常见(43.5%),同时伴有囊膜渗透、不规则生长、假性足、脂肪瘤样改变和血管渗透。97例(93.3%)出现假恶性细胞形态特征,表现为细胞增多、细胞异型、增殖活性增强、嗜瘤细胞化生、坏死。此外,30例(28.8%)表现出与其他恶性唾液腺肿瘤相似的特征,特别是肌上皮癌、腺样囊性癌和多形腺癌。尽管PA的诊断通常很简单,但具有这些特征的病例可能被错误地解释为恶性肿瘤。共同的形态细胞学特征强调了准确诊断的复杂性,强调需要细致的检查和全面的评估,结合形态学,分子和免疫组织化学分析来区分良性和恶性唾液腺肿瘤,在选定的病例中。
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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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