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Paget 骨病中的多灶性破骨细胞丰富肿瘤与传统的巨细胞瘤,两种在遗传学上截然不同的实体?来自单个病例的测序。

Multifocal osteoclast-rich tumour in Paget bone disease and conventional giant cell tumour, two genetically distinct entities? Sequencing from a single case.

机构信息

Research Department of Pathology, University College London, UCL Cancer Institute, WC1E 6BT, London, UK.

Cellular and Molecular Pathology, Royal National Orthopaedic Hospital, Greater London, Stanmore, UK.

出版信息

Skeletal Radiol. 2024 Jan;53(1):175-178. doi: 10.1007/s00256-023-04369-6. Epub 2023 Jun 13.

Abstract

Paget disease of bone is a metabolic disorder with a strong genetic component, characterised by pronounced disorganised bone remodelling. Complications of this disease include an increased risk of developing bone neoplasms. Here, we describe the case of a 60-year-old Italian patient with Paget disease of bone, presenting with an osteoclast-rich tumour. Our analysis of this entity, based on the clinical, morphological and genetic data (whole exome sequencing), suggests that osteoclast-rich lesions in Paget disease of bone are genetically distinct from classical giant cell tumour of bone. We discuss the importance of differentiating these osteoclast-rich lesions.

摘要

骨 Paget 病是一种具有强烈遗传成分的代谢性疾病,其特征为明显的骨改建紊乱。该疾病的并发症包括发生骨肿瘤的风险增加。在此,我们描述了一例 60 岁的意大利患者患有骨 Paget 病,表现为破骨细胞丰富的肿瘤。我们基于临床、形态学和遗传数据(全外显子组测序)对该实体进行了分析,结果表明,骨 Paget 病中的破骨细胞丰富病变在遗传上与经典的骨巨细胞瘤不同。我们讨论了区分这些破骨细胞丰富病变的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/774e/10661784/def6ce142a30/256_2023_4369_Fig1_HTML.jpg

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