Suppr超能文献

不明原因的心脏肥大作为浆细胞瘤的线索:一项病例研究。

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

作者信息

Liu Sha, Tong Chengbi, Xie Junmin, Zang Shasha

机构信息

Department of Cardiology, Affiliated Hospital of Hebei University Baoding 071000, Hebei, China.

Department of Laboratory, Affiliated Hospital of Hebei University Baoding 071000, Hebei, China.

出版信息

Am J Transl Res. 2025 Jul 15;17(7):5195-5201. doi: 10.62347/YWDH3068. eCollection 2025.

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.

摘要

初步诊断

一名60岁男性最初表现为胸闷、疲劳和心律失常。浆细胞瘤的指征:初始影像学检查提示因心肌增厚导致淀粉样变性。磁共振成像(MRI)显示左心室肥厚及延迟强化,同时κ:λ比值升高,引发了对浆细胞瘤的怀疑。浆细胞瘤的确诊:进一步的诊断测试,包括免疫固定电泳和心肌活检,确诊为浆细胞瘤。患者被诊断为轻链(AL)淀粉样变性,这是浆细胞瘤的一种亚型,通过骨髓活检和免疫组织化学得以证实。治疗:使用硼替佐米、地塞米松和达雷妥尤单抗治疗后,症状得到显著改善。结论:该病例强调了在不明原因的心脏肥大中考虑浆细胞疾病的重要性,并突出了早期诊断策略和靶向治疗的必要性。

相似文献

1
Unexplained cardiac hypertrophy as a clue to plasma cell tumour: a case study.
Am J Transl Res. 2025 Jul 15;17(7):5195-5201. doi: 10.62347/YWDH3068. eCollection 2025.
2
Atypical Presentation of Systemic Amyloid Light Chain (AL) Amyloidosis.
Cureus. 2025 Jun 11;17(6):e85777. doi: 10.7759/cureus.85777. eCollection 2025 Jun.
3
Multimodality imaging features of systemic amyloidosis: a case report.
BMC Cardiovasc Disord. 2025 Jan 2;25(1):1. doi: 10.1186/s12872-024-04441-6.
8
An atypical cause of amyloidosis: a case of combined heavy and light chain amyloidosis.
BMC Nephrol. 2025 Jul 1;26(1):332. doi: 10.1186/s12882-025-04226-9.
10
Relevance of Prescribing Serum Immunofixation Electrophoresis in the Diagnosis of Monoclonal Gammopathies.
Cureus. 2025 Jun 19;17(6):e86339. doi: 10.7759/cureus.86339. eCollection 2025 Jun.

本文引用的文献

3
Advanced Imaging in Cardiac Amyloidosis.
Biomedicines. 2022 Apr 15;10(4):903. doi: 10.3390/biomedicines10040903.
5
Cardiac lymphoma with early response to chemotherapy: A case report and review of the literature.
J Nucl Cardiol. 2022 Dec;29(6):3044-3056. doi: 10.1007/s12350-021-02570-5. Epub 2021 Mar 11.
6
Long-Term Electrocardiographic Follow-Up of a Patient with Light-Chain Cardiac Amyloidosis.
J Nippon Med Sch. 2022 Mar 11;89(1):119-125. doi: 10.1272/jnms.JNMS.2022_89-111. Epub 2021 Mar 9.
7
Myocardial amyloidosis following multiple myeloma in a 38-year-old female patient: A case report.
Open Med (Wars). 2020 May 16;15(1):396-402. doi: 10.1515/med-2020-0125. eCollection 2020.
8
Diagnosis and treatment of cardiac amyloidosis: an interdisciplinary consensus statement.
Wien Klin Wochenschr. 2020 Dec;132(23-24):742-761. doi: 10.1007/s00508-020-01781-z. Epub 2020 Dec 3.
9
Bortezomib, Melphalan, and Dexamethasone for Light-Chain Amyloidosis.
J Clin Oncol. 2020 Oct 1;38(28):3252-3260. doi: 10.1200/JCO.20.01285. Epub 2020 Jul 30.
10
Kappa-light Chain Amyloid Overlapping Hypertrophic Cardiomyopathy With Myocardial Noncompaction.
Circ Cardiovasc Imaging. 2020 Jul;13(7):e010379. doi: 10.1161/CIRCIMAGING.119.010379. Epub 2020 Jul 1.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验