Compressive Myeloradiculopathies in Multiple Myeloma: Clinical and Radiological Characteristics of a Series of 29 Patients
E. Niang, M. Bamba, K. Mamadou, F. Seynabou, Seck Moussa, M. Ababacar, Bousso Elimane, Sarr Khadim, Faye Atoumane, Ndiaye Fatou Samba Diago, N. Moustapha, Diop Saliou
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Abstract
Introduction: Patients with multiple myeloma (MM) develop neurological complications such as root and/or spinal cord compression in at least 5% of cases. The aim of this work is to describe the clinical and radiological features of root and/or spinal cord compression occurring during multiple myeloma. Patients and Methods: We conducted a retrospective study in the Clinical Haematology Department of Dalal Jamm Hospital and the National Blood Transfusion Centre, the Neurological Clinic of Fann Hospital Centre and the Internal Medicine Department of Aristide Le Dantec Hospital in Dakar between January 2016 and December 2019. All patients whose multiple myeloma diagnosis was established according to the International Myeloma Working Group’s 2014 and who had root, spinal or myeloradicular compression, were included in our study. Results: A total of 29 patients were included. The average age was 54.31 years [32 76 years]. The sex ratio (M/F) was 1.6. Motor deficits were the reason for consultation in 68% of the patients and spinal pains were reported by 93% of the patients. Neurological signs revealed multiple myeloma in all our patients. 25 patients (86.2%) had paraplegia and 1 patient had tetraparesis. Hypoesthesia to a defined sensory level was noted in 8 patients (28%). 5 patients (17.24%) had sphincter disorders. The types of lesions showed by imaging were vertebral lysis in 100% of cases, vertebral compression in 37% of cases, and epidural infiltration in 34% of cases. 12 patients (41.37%) had spinal compression, 14 patients (48.27%) had root compression, and 3 patients (10.34%) had myeloradicular compression. Spinal cord compression was most often at the dorsolumbar level (91.3% of cases) and root compression was How to cite this paper: Niang, E.H.D., Bamba, M.A., Mamadou, K., Seynabou, F., Moussa, S., Ababacar, M.K., Elimane, B., Khadim, S., Atoumane, F., Diago, N.F.S., Moustapha, N. and Saliou D. (2021) Compressive Myeloradiculopathies in Multiple Myeloma: Clinical and Radiological Characteristics of a Series of 29 Patients. Open Journal of Blood Diseases, 11, 133-139. https://doi.org/10.4236/ojbd.2021.114013 Received: January 17, 2021 Accepted: November 29, 2021 Published: December 2, 2021 Copyright © 2021 by author(s) and Scientific Research Publishing Inc. This work is licensed under the Creative Commons Attribution International License (CC BY 4.0). http://creativecommons.org/licenses/by/4.0/ Open Access
多发性骨髓瘤的压迫性髓根病:29例患者的临床和放射学特征
简介:多发性骨髓瘤(MM)患者出现神经系统并发症,如根和/或脊髓压迫至少5%的病例。本研究的目的是描述多发性骨髓瘤期间发生的根和/或脊髓压迫的临床和放射学特征。患者和方法:我们于2016年1月至2019年12月在达喀尔Dalal Jamm医院和国家输血中心的临床血化科、Fann医院中心的神经病学诊所和Aristide Le Dantec医院的内科进行了一项回顾性研究。所有根据国际骨髓瘤工作组(International myeloma Working Group) 2014年的诊断确定的多发性骨髓瘤患者,以及有根、脊髓或髓根压迫的患者都被纳入我们的研究。结果:共纳入29例患者。平均年龄54.31岁[32 76岁]。性别比(M/F)为1.6。68%的患者因运动障碍就诊,93%的患者因脊柱疼痛就诊。所有病人的神经学症状都显示多发性骨髓瘤。截瘫25例(86.2%),四肢全瘫1例。8例(28%)患者感觉减退至定义的感觉水平。括约肌病变5例(17.24%)。影像学显示的病变类型为100%的椎体松解,37%的椎体受压,34%的硬膜外浸润。脊柱受压12例(41.37%),根受压14例(48.27%),髓根受压3例(10.34%)。脊髓受压最常发生在腰背水平(91.3%的病例),而根受压主要发生在以下部位:引用本文:Niang, e.h.d., Bamba, m.a., Mamadou, K, Seynabou, F, Moussa, S, Ababacar, m.k., Elimane, B, Khadim, S, Atoumane, F, Diago, N.F.S, Moustapha, N.和Saliou D.(2021)多发性骨髓瘤的压迫性脊髓根病变:29例患者的临床和放射学特征。中华血液病杂志,11,133-139。https://doi.org/10.4236/ojbd.2021.114013收稿日期:2021年1月17日收稿日期:2021年11月29日出版日期:2021年12月2日版权所有©作者与科研出版公司。本作品采用知识共享署名国际许可协议(CC BY 4.0)。http://creativecommons.org/licenses/by/4.0/开放获取
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