The value of morphology: osteoclast-like cells in soft tissue tumours.

IF 2.3 4区 医学 Q3 ONCOLOGY
Pathology & Oncology Research Pub Date : 2025-09-12 eCollection Date: 2025-01-01 DOI:10.3389/pore.2025.1612175
Ali Al Khader, Christian Seghetti, Fatine Oumlil, Anna Tollit, Roberto Tirabosco, Fernanda Amary, Paul O'Donnell, Adrienne M Flanagan
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引用次数: 0

Abstract

Recognition of unusual histological features can augment and hasten a diagnosis but also stimulate ideas about physiological and pathological cellular interactions. Osteoclasts resorb mineralised tissue and therefore can be found at sites of heterotopic bone formation. However, multinucleated giant cells with morphological features of osteoclasts, so called 'osteoclast-like cells' can also be encountered in a variety of soft tissue tumours unrelated to ossification and calcification. Prompted by the presence of osteoclast-like cells in undifferentiated pleomorphic sarcoma while undertaking our Artificial Intelligence project for classifying sarcoma, we reviewed the English literature for these cells in soft tissue tumours and we found that this was poorly documented, and much was published before the release of the WHO essential diagnostic criteria in 2020. There were numerous single case reports and small series of a broad range of soft tissue tumours with osteoclast-like cells but only a limited number of diagnoses in which these cells were reported recurrently. We provide a comprehensive update of osteoclast-like cells and mineralisation in soft tissue tumours from the literature. We also present real-world incidence of osteoclast-like cells from selected tumour types in our Whole Slide Image (WSI) library of soft tissue tumours. Assessment of WSI from 1100 different patients showed that osteoclast-like cells were relatively common and under-recognised in nodular fasciitis (18.5 of 200), angiomatoid fibrous histiocytoma (17.5% of 40), undifferentiated pleomorphic sarcoma (15% of 261) and epithelioid sarcoma (9% of 68) while they were never encountered in myxofibrosarcoma (0/250) and clear cell sarcoma of soft tissue (0/80). Awareness of this phenomenon not only helps shape the differential diagnosis but also can be used to stimulate pathobiological questions and to enhance the performance of AI models for classifying disease.

形态学的价值:软组织肿瘤中的破骨细胞样细胞。
识别不寻常的组织学特征可以增强和加速诊断,但也激发了生理和病理细胞相互作用的想法。破骨细胞吸收矿化组织,因此可以在异位骨形成的部位发现。然而,具有破骨细胞形态特征的多核巨细胞,即所谓的“破骨细胞样细胞”,也可以在各种与骨化和钙化无关的软组织肿瘤中发现。在进行肉瘤分类的人工智能项目时,由于未分化多形性肉瘤中存在破骨细胞样细胞,我们回顾了软组织肿瘤中这些细胞的英文文献,我们发现这方面的文献很少,并且在2020年世卫组织基本诊断标准发布之前发表了很多。有大量的单一病例报告和小范围的软组织肿瘤与破骨细胞样细胞,但只有有限数量的诊断报告这些细胞复发。我们从文献中提供了软组织肿瘤中破骨细胞样细胞和矿化的全面更新。我们还在软组织肿瘤的全幻灯片图像(WSI)文库中展示了来自选定肿瘤类型的破骨细胞样细胞的真实发病率。来自1100名不同患者的WSI评估显示,破骨细胞样细胞在结节性筋膜炎(200例中18.5例)、血管瘤样纤维组织细胞瘤(40例中17.5%)、未分化多形性肉瘤(261例中15%)和上皮样肉瘤(68例中9%)中相对常见且未被识别,而在黏液纤维肉瘤(0/250)和软组织透明细胞肉瘤(0/80)中从未见过。对这一现象的认识不仅有助于形成鉴别诊断,而且可以用来激发病理生物学问题,并提高人工智能模型对疾病进行分类的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
134
审稿时长
4-8 weeks
期刊介绍: Pathology & Oncology Research (POR) is an interdisciplinary Journal at the interface of pathology and oncology including the preclinical and translational research, diagnostics and therapy. Furthermore, POR is an international forum for the rapid communication of reviews, original research, critical and topical reports with excellence and novelty. Published quarterly, POR is dedicated to keeping scientists informed of developments on the selected biomedical fields bridging the gap between basic research and clinical medicine. It is a special aim for POR to promote pathological and oncological publishing activity of colleagues in the Central and East European region. The journal will be of interest to pathologists, and a broad range of experimental and clinical oncologists, and related experts. POR is supported by an acknowledged international advisory board and the Arányi Fundation for modern pathology.
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