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