Olagunju Abdulbaril, Shekar Chandana, Morris Michael, Kalya Anantharam, Mookadam Farouk, Unzek Samuel
Department of Medicine, Creighton University, Phoenix, AZ, USA.
Heart Center, Banner University Medical Center, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
Case Rep Cardiol. 2022 Jul 30;2022:7846846. doi: 10.1155/2022/7846846. eCollection 2022.
We report a case of a 57-year-old woman with a history of multiple myeloma (MM) and light chain (AL) amyloidosis who presented due to worsening dyspnea on exertion. Her MM has been refractory to multiple chemotherapy regimens and two autologous bone marrow transplantation. Diagnostic evaluations including serum kappa and lambda chains, echocardiogram, pyrophosphate cardiac scan, and cardiac magnetic resonance were indicative of a progression to AL cardiomyopathy. Addition of daratumumab to her regimen appeared to ameliorate the progression of AL cardiomyopathy. However, it was stopped due to adverse effects of pancytopenia and allergic reactions including skin rash and hives. She was hospitalized for heart failure exacerbation and died approximately 2 months following the discontinuation of daratumumab. This case highlights the late presentation of AL cardiomyopathy in refractory MM.
我们报告一例57岁女性,有多发性骨髓瘤(MM)和轻链(AL)淀粉样变性病史,因劳力性呼吸困难加重就诊。她的MM对多种化疗方案及两次自体骨髓移植均耐药。包括血清κ和λ链、超声心动图、焦磷酸盐心肌扫描及心脏磁共振在内的诊断评估表明已进展为AL心肌病。在她的治疗方案中加用达雷妥尤单抗似乎改善了AL心肌病的进展。然而,因全血细胞减少及包括皮疹和荨麻疹在内的过敏反应等不良反应而停药。她因心力衰竭加重住院,在停用达雷妥尤单抗后约2个月死亡。该病例突出了难治性MM中AL心肌病的晚期表现。