Tahan Ihssan, Seale Jim, Edwards David
Bone marrow transplant unit, Bristol Royal Hospital for Children, Upper maudlin street, Bristol, BS2 8BJ, UK.
Cases J. 2008 Oct 2;1(1):207. doi: 10.1186/1757-1626-1-207.
IgM multiple myeloma is rare disorder, which has clinical, laboratory and radiological manifestations that are consistent with both multiple myeloma and Waldenstrom's macroglobulinaemia.
An 83 years Welsh lady presented with clinical and radiological features consistent with spinal cord compression. Further investigations confirmed the diagnosis of IgM multiple myeloma. Following localized radiotherapy and five courses of melphalan and prednisolone, the patient achieved partial remission of her myeloma. Later on, the patient had disease progression in the form of rising serum IgM level and the development of multiple plasmacytomas. She was treated with thalidomide, cyclophosphamide, dexamethasone and radiotherapy, which resulted in the control of her disease for one year. To our knowledge, this is the second case of IgM myeloma presenting with a plasmacytoma and the first case of IgM myeloma presenting with cord compression caused by plasmacytomas.
Unlike other types of multiple myeloma IgM myeloma is rarely complicated by plasmacytomas. However, spinal cord compression caused by plasmacytomas in this type of myeloma is extremely rare. Nevertheless, the same lines of management, e.g. cytotoxic chemotherapy and local radiotherapy that are applied to other types of myeloma can be successfully utilized.
IgM 型多发性骨髓瘤是一种罕见疾病,其临床、实验室及影像学表现与多发性骨髓瘤和华氏巨球蛋白血症均相符。
一位83岁的威尔士女性患者表现出与脊髓压迫相符的临床及影像学特征。进一步检查确诊为 IgM 型多发性骨髓瘤。经过局部放疗以及五个疗程的美法仑和泼尼松治疗后,患者的骨髓瘤病情部分缓解。后来,患者病情进展,血清 IgM 水平升高且出现多个浆细胞瘤。她接受了沙利度胺、环磷酰胺、地塞米松及放疗治疗,病情得到控制达一年。据我们所知,这是第二例伴有浆细胞瘤的 IgM 型骨髓瘤病例,也是首例由浆细胞瘤导致脊髓压迫的 IgM 型骨髓瘤病例。
与其他类型的多发性骨髓瘤不同,IgM 型骨髓瘤很少并发浆细胞瘤。然而,这种类型的骨髓瘤由浆细胞瘤导致脊髓压迫极为罕见。尽管如此,应用于其他类型骨髓瘤的相同治疗方法,如细胞毒性化疗和局部放疗,在此也可成功应用。