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病例报告:具有临床意义的单克隆丙种球蛋白病相关性肌病:基于病例的综述

Case Report: Monoclonal Gammopathies of Clinical Significance-Associated Myopathy: A Case-Based Review.

作者信息

Yu Hongbin, He Du, Zhang Qing, Cao Bei, Liu Weiping, Wu Yu

机构信息

Department of Hematology, West China Hospital, Sichuan University, Chengdu, China.

Department of Pathology, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Front Oncol. 2022 Jul 14;12:914379. doi: 10.3389/fonc.2022.914379. eCollection 2022.

Abstract

Monoclonal gammopathies of clinical significance (MGCS)-associated myopathy is a group of muscular MGCS-based rare manifestations. It mainly includes amyloid light chain (AL) amyloidosis and sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance. When myopathy manifests as the initial or sole clinical symptom, it can often be delayed or misdiagnosed as other myopathies. We report the case of a 60-year-old man who initially presented with fatigue and muscle weakness of the symmetric proximal lower limbs. Muscle biopsy did not reveal mononuclear cell infiltration, atrophy, necrosis, or positive Congo red staining results. The results of serum protein electrophoresis and immunofixation electrophoresis were negative. No specific diagnosis was established. After 1 year, the patient was diagnosed with AL amyloidosis after myocardial and fat pad biopsies were performed and myopathy was diagnosed as AL amyloidosis-associated myopathy after reassessment. The patient received CyBorD regime chemotherapy and achieved hematological and organ remission. Therefore, we reviewed the clinical and pathological manifestations of MGCS-associated myopathies. Based on published articles and the present case, we conclude that comprehensive screening for MGCS in unexplained myopathy is essential to avoid misdiagnosis or delayed diagnosis.

摘要

具有临床意义的单克隆丙种球蛋白病(MGCS)相关肌病是一组基于MGCS的罕见肌肉表现。它主要包括淀粉样轻链(AL)淀粉样变性和意义未明的单克隆丙种球蛋白病相关的散发性晚发型杆状体肌病。当肌病表现为初始或唯一临床症状时,它常常会被延迟诊断或误诊为其他肌病。我们报告了一例60岁男性患者,其最初表现为双侧对称的近端下肢疲劳和肌无力。肌肉活检未发现单核细胞浸润、萎缩、坏死或刚果红染色阳性结果。血清蛋白电泳和免疫固定电泳结果均为阴性。未明确诊断。1年后,在进行心肌和脂肪垫活检后,患者被诊断为AL淀粉样变性,重新评估后,肌病被诊断为AL淀粉样变性相关肌病。该患者接受了CyBorD方案化疗并实现了血液学和器官缓解。因此,我们回顾了MGCS相关肌病的临床和病理表现。基于已发表的文章和本病例,我们得出结论,对不明原因的肌病进行MGCS的全面筛查对于避免误诊或延迟诊断至关重要。

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