甲状腺梭形病变:细胞学和组织学回顾。

IF 3.1 3区 医学 Q1 PATHOLOGY
Virchows Archiv Pub Date : 2025-06-01 Epub Date: 2025-04-11 DOI:10.1007/s00428-025-04095-5
Angela Feraco, Federica Vegni, Belen Padial Urtueta, Qianqian Zhang, Elena Navarra, Antonino Mule, Liron Pantanowitz, Esther Diana Rossi
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引用次数: 0

摘要

大多数甲状腺病变是上皮性的,表现为典型的滤泡和/或乳头状生长模式。主要梭形细胞病变的发生在甲状腺是罕见的,很可能在细胞学或组织学样本中被误诊,这可能影响患者的管理。诊断是通过发现大量梭形细胞,在某些情况下可能与其他形态学特征相结合。重要的是要识别这些梭形细胞是否具有良性或恶性的特征。这类病变的鉴别诊断包括间质肿瘤(如孤立性纤维性肿瘤)和非间质肿瘤(如间变性甲状腺癌)。由于其罕见性、病理学家经验有限、细胞形态特征重叠以及选择和解释适当的辅助研究的挑战,对此类病变的形态学解释可能存在问题。本文讨论了大多数显示梭形细胞特征的甲状腺实体,强调了它们的细胞学和组织学发现与最近Bethesda系统报告的甲状腺细胞病理学和WHO内分泌肿瘤分类的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spindle lesions in the thyroid: a cytological and histological review.

The majority of thyroid lesions are of epithelial origin that exhibit a typical follicular and/or papillary growth pattern. The occurrence of a predominantly spindle cell lesion is uncommon in the thyroid gland and is likely to be misdiagnosed in cytological or histological samples, which may impact patient management. The diagnosis is made by finding a significant amount of spindle cells, which may be combined in some cases with other morphologic features. It is important to recognize if these spindle cells have benign or malignant features. The differential diagnosis for such lesions includes mesenchymal neoplasms (e.g., solitary fibrous tumor) and non-mesenchymal tumors (e.g., anaplastic thyroid carcinoma). The morphologic interpretation of such lesions can be problematic due to their rarity, pathologists' limited experience, overlapping cytomorphologic features, and challenges selecting and interpreting appropriate ancillary studies. This review discusses most of the thyroid entities showing spindle cell features, emphasizing their cytological and histological findings of relevance to the recent Bethesda system for reporting thyroid cytopathology and WHO classification of endocrine tumors.

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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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