Unexplained cardiac hypertrophy as a clue to plasma cell tumour: a case study.

IF 1.6 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
American journal of translational research Pub Date : 2025-07-15 eCollection Date: 2025-01-01 DOI:10.62347/YWDH3068
Sha Liu, Chengbi Tong, Junmin Xie, Shasha Zang
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引用次数: 0

Abstract

Initial diagnosis: A 60-year-old male presented with initial diagnosis chest tightness, fatigue, and arrhythmia. Indications for plasma cell tumour: Initial imaging suggested amyloidosis due to myocardial thickening. Left ventricular hypertrophy and delayed enhancement on Magnetic Resonance Imaging (MRI), along with an elevated κ:λ ratio, raising suspicion for a plasma cell tumour. Confirmation of the plasma tumour: Further diagnostic tests, including immunofixation electrophoresis and myocardial biopsy, confirmed a plasma cell tumour. The patient was diagnosed with light chain (AL) amyloidosis, a subtype of plasma cell tumor, confirmed by bone marrow biopsy and immunohistochemistry. Treatment: Treatment with bortezomib, dexamethasone, and daratumumab resulted in significant symptomatic improvement. Conclusion: This case underscores the importance of considering plasma cell disorders in unexplained cardiac hypertrophy and highlights the need for early diagnostic strategies and targeted therapies.

不明原因的心肌肥大作为浆细胞肿瘤的线索:一个案例研究。
初诊:男性,60岁,初诊胸闷,乏力,心律失常。浆细胞瘤的适应症:初步影像学提示心肌增厚引起淀粉样变。左心室肥厚和磁共振成像(MRI)延迟增强,同时κ:λ比值升高,增加对浆细胞肿瘤的怀疑。确认浆细胞瘤:进一步的诊断试验,包括免疫固定电泳和心肌活检,确认浆细胞瘤。经骨髓活检和免疫组织化学证实,患者被诊断为轻链(AL)淀粉样变,浆细胞肿瘤的一种亚型。治疗:用硼替佐米、地塞米松和达拉单抗治疗可显著改善症状。结论:该病例强调了在不明原因的心肌肥厚中考虑浆细胞疾病的重要性,并强调了早期诊断策略和靶向治疗的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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