Crystal induced arthropathies—a comparative study of 40 patients with apatite rheumatism, chondrocalcinosis and primary synovial chondromatosis

M. Bély, A. Apathy
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Abstract

Introduction: Apatite rheumatism (AR), chondrocalcinosis (Ch-C), and primary synovial chondromatosis (prSynCh) are regarded as distinct clinical entities. The introduction of the non-staining technique by Bély and Apáthy (2013) opened a new era in the microscopic diagnosis of crystal induced diseases, allowing the analysis of MSU (monosodium urate monohydrate) HA (calcium hydroxyapatite), CPPD (calcium pyrophosphate dihydrate) crystals, cholesterol, crystalline liquid lipid droplets, and other crystals in unstained sections of conventionally proceeded (aqueous formaldehyde fixed, paraffin-embedded) tissue samples. The aim of this study was to describe the characteristic histology of crystal deposits in AR, Ch-C, and prSynCh with traditional stains and histochemical reactions comparing with unstained tissue sections according to Bély and Apáthy (2013).Patients and methods: Tissue samples of 4 with apatite rheumatism (Milwaukee syndrome), 16 with chondrocalcinosis, and 20 with clinically diagnosed primary synovial chondromatosis were analyzed.Results and conclusion: Apatite rheumatism, chondrocalcinosis, and primary synovial chondromatosis are related metabolic disorders with HA and CPPD depositions. The authors assume that AR and Ch-C are different stages of the same metabolic disorder, which differ from prSynCh in amorphous mineral production, furthermore in the production of chondroid, osteoid and/or bone. prSynCh is a defective variant of HA and CPPD induced metabolic disorders with reduced mineralization capabilities, where the deficient mineralization is replaced by chondroid and/or bone formation. The non-staining technique of Bély and Apáthy proved to be a much more effective method for the demonstration of crystals in metabolic diseases than conventional stains and histochemical reactions.
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晶体诱发的关节病--对 40 名磷灰石风湿病、软骨钙化病和原发性滑膜软骨瘤病患者的比较研究
导言:磷灰石风湿病(AR)、软骨钙化病(Ch-C)和原发性滑膜软骨瘤病(prSynCh)被视为不同的临床实体。Bély和Apáthy(2013年)引入的无染色技术开创了晶体诱发疾病显微诊断的新纪元,可对MSU(一水尿酸单钠)、HA(羟基磷灰石钙)进行分析、CPPD(焦磷酸二水钙)晶体、胆固醇、结晶液脂滴和其他晶体。本研究的目的是根据 Bély 和 Apáthy(2013 年)的观点,通过传统染色和组织化学反应与未染色的组织切片进行比较,描述 AR、Ch-C 和 prSynCh 晶体沉积的组织学特征:分析了 4 例磷灰石风湿症(密尔沃基综合征)患者、16 例软骨钙化症患者和 20 例临床诊断为原发性滑膜软骨瘤病患者的组织样本:结果和结论:磷灰石风湿病、软骨钙化症和原发性滑膜软骨瘤病是与 HA 和 CPPD 沉积相关的代谢性疾病。作者认为,AR 和 Ch-C 是同一种代谢性疾病的不同阶段,它们与 prSynCh 的不同之处在于非晶体矿物质的生成,以及软骨、类骨和/或骨的生成。prSynCh 是由 HA 和 CPPD 引起的代谢性疾病的缺陷变体,其矿化能力降低,不足的矿化被软骨和/或骨的形成所取代。事实证明,与传统染色法和组织化学反应相比,Bély 和 Apáthy 的无染色技术是一种更有效的方法来显示代谢性疾病中的晶体。
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