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原发性滑膜软骨瘤病:155例恶性潜能的重新评估

Primary synovial chondromatosis: a reassessment of malignant potential in 155 cases.

作者信息

McCarthy C, Anderson W J, Vlychou M, Inagaki Y, Whitwell D, Gibbons C L M H, Athanasou N A

机构信息

Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal and Sciences, University of Oxford, Nuffield Orthopaedic Centre, Oxford, OX3 7HE, UK.

出版信息

Skeletal Radiol. 2016 Jun;45(6):755-62. doi: 10.1007/s00256-016-2353-3. Epub 2016 Feb 27.

Abstract

OBJECTIVE

Primary synovial chondromatosis (PSC) is a rare disorder characterised by cartilage formation in synovium-lined joints, tendon sheaths and bursae. It is thought that PSC cartilage arises from the proliferation of mesenchymal cells, which exhibit cartilaginous metaplasia in subintimal connective tissue. There are reports of transformation of PSC to chondrosarcoma, although the precise incidence and nature of this complication is uncertain. In this study we carried out a retrospective review PSC to determine the incidence of sarcomatous change in this condition, in addition to the clinical, radiological and pathological features that characterise this complication

MATERIALS AND METHODS

We reviewed 155 cases of PSC and identified 4 cases (3 in the hip joint; 1 in the elbow joint) of aggressive behaviour and chondrosarcoma-like histology.

RESULTS

Radiologically, these cases were all reported as showing features consistent with PSC and aggressive extra-articular soft tissue/bone involvement. Histologically, in addition to typical features of PSC, there was morphological evidence of peri-articular soft tissue and, in 2 cases, bone involvement by an infiltrating cartilaginous tumour. These tumours all behaved as locally aggressive neoplasms and did not give rise to metastasis.

CONCLUSION

Our findings show that chondrosarcoma arises infrequently in PSC (approximately 2.5 %), and that this complication occurs most commonly in the hip joint (approximately 11 % of cases of hip PSC). These tumours behaved mainly as low-grade, locally aggressive tumours analogous to atypical cartilaginous tumour of bone/grade 1 chondrosarcoma of bone.

摘要

目的

原发性滑膜软骨瘤病(PSC)是一种罕见疾病,其特征为在滑膜衬里的关节、腱鞘和滑囊中形成软骨。据认为,PSC软骨起源于间充质细胞的增殖,这些细胞在内膜下结缔组织中表现出软骨化生。有关于PSC转变为软骨肉瘤的报道,尽管这种并发症的确切发生率和性质尚不确定。在本研究中,我们对PSC进行了回顾性研究,以确定这种情况下肉瘤样改变的发生率,以及表征这种并发症的临床、放射学和病理学特征。

材料与方法

我们回顾了155例PSC病例,确定了4例(3例发生在髋关节;1例发生在肘关节)具有侵袭性行为和软骨肉瘤样组织学表现的病例。

结果

在放射学上,这些病例均报告显示出与PSC一致的特征以及关节外软组织/骨的侵袭性受累。在组织学上,除了PSC的典型特征外,还有关节周围软组织的形态学证据,在2例病例中,有浸润性软骨肿瘤累及骨。这些肿瘤均表现为局部侵袭性肿瘤,未发生转移。

结论

我们的研究结果表明,软骨肉瘤在PSC中很少发生(约2.5%),这种并发症最常见于髋关节(约占髋关节PSC病例的11%)。这些肿瘤主要表现为低级别、局部侵袭性肿瘤,类似于骨非典型软骨肿瘤/骨1级软骨肉瘤。

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