Al Hadidi Samer, Katato Khalil, Bachuwa Ghassan
aMichigan State University, Flint, MI, USA.
bHurley Medical Center, Flint, MI, USA.
Case Rep Oncol. 2017 Mar 29;10(1):272-275. doi: 10.1159/000466687. eCollection 2017 Jan-Apr.
Immunoglobulin D multiple myeloma is a rare type of multiple myeloma that usually presents as bone pain, fatigue, or weight loss. We report a case of immunoglobulin D multiple myeloma in a 53-year-old Caucasian male patient with previous medical history of anaplastic oligodendroglioma status post-surgical resection who was evaluated for back pain while mowing the lawn. His physical examination showed tenderness over the lower thoracic vertebrae with no sensory or motor impairment. Initial lab investigations showed normocytic anemia and hypercalcemia with low parathyroid hormone. Magnetic resonance imaging of thoracic spine with and without contrast showed acute pathological fracture of the T12 vertebral body with enhancing soft tissue which extended into the left ventral epidural space and left T11-T12 neural foramen. Serum protein electrophoresis showed abnormal protein band in the gamma globulin. Free light chain assay showed serum free kappa which was elevated at 3,090.0 mg/L (reference range 3.3-19.4 mg/L). Immunoglobulin D was elevated at 566.0 mg/dL (reference range <15.3 mg/dL). The patient was successfully treated with standard chemotherapy and autologous peripheral blood stem cell transplant with complete remission 3 years after starting treatment. Advancement in the treatment of immunoglobulin D multiple myeloma urge clinicians to offer their patients new treatment options especially as of the earlier presentation of this subtype of multiple myeloma and the previous reports of worse prognosis.
免疫球蛋白D型多发性骨髓瘤是一种罕见的多发性骨髓瘤,通常表现为骨痛、疲劳或体重减轻。我们报告一例53岁的白种男性免疫球蛋白D型多发性骨髓瘤患者,该患者既往有间变性少突胶质细胞瘤手术切除病史,在修剪草坪时因背痛接受评估。体格检查显示下胸椎有压痛,无感觉或运动障碍。初始实验室检查显示正细胞性贫血、高钙血症伴甲状旁腺激素水平低。胸椎磁共振成像平扫及增强显示T12椎体急性病理性骨折,有强化的软组织,延伸至左腹侧硬膜外间隙及左T11 - T12椎间孔。血清蛋白电泳显示γ球蛋白区有异常蛋白条带。游离轻链检测显示血清游离κ链升高,为3090.0mg/L(参考范围3.3 - 19.4mg/L)。免疫球蛋白D升高至566.0mg/dL(参考范围<15.3mg/dL)。该患者接受标准化疗和自体外周血干细胞移植治疗成功,治疗开始3年后完全缓解。免疫球蛋白D型多发性骨髓瘤治疗的进展促使临床医生为患者提供新的治疗选择,尤其是考虑到这种多发性骨髓瘤亚型的更早表现以及既往预后较差的报道。