Haegelen Claire, Riffaud Laurent, Bernard Marc, Carsin-Nicol Beatrice, Morandi Xavier
Department of Neurosurgery, Pontchaillou Hospital, Rennes, France.
J Neurosurg. 2006 Apr;104(4):608-10. doi: 10.3171/jns.2006.104.4.608.
The authors describe the case of a 72-year-old woman with dural plasmacytoma revealing an immunoglobulin (Ig) G-kappa multiple myeloma (MM). She presented with headaches and left hemiparesis. Magnetic resonance imaging demonstrated a right frontal extraaxial lesion arising from the dura mater, and biological studies revealed hypercalcemia, hyperproteinemia, and a serum gamma globulin peak. A diagnosis of IgG-kappa MM was based on microscopic examination and immunohistochemical analysis of the dural plasmacytoma as well as on signs of systemic myeloma after surgery. The patient died 3 years after the first symptoms of MM despite systemic chemotherapy and no recurrence of the dural plasmacytoma. Myelomatous involvement of the dura mater is a rare occurrence given that only three cases have been reported to date. Nevertheless, this pathological entity should be differentiated from solitary dural plasmacytoma (SDP) because the prognosis is radically different. Progression seems to be correlated with systemic disease in contrast to the long-term survival associated with SDP. Careful systemic evaluation should be made in such a presentation to rule out MM, which would require different management and has a different prognosis.
作者描述了一例72岁患有硬脑膜浆细胞瘤的女性病例,该病例显示为免疫球蛋白(Ig)G-κ多发性骨髓瘤(MM)。她表现为头痛和左侧偏瘫。磁共振成像显示一个起源于硬脑膜的右侧额部轴外病变,生物学检查显示高钙血症、高蛋白血症和血清γ球蛋白峰值。IgG-κ MM的诊断基于硬脑膜浆细胞瘤的显微镜检查和免疫组化分析以及术后系统性骨髓瘤的体征。尽管进行了全身化疗且硬脑膜浆细胞瘤未复发,但患者在出现MM的首发症状3年后死亡。鉴于迄今为止仅报道了3例,硬脑膜的骨髓瘤累及是一种罕见情况。然而,这种病理实体应与孤立性硬脑膜浆细胞瘤(SDP)相鉴别,因为预后截然不同。与SDP相关的长期生存相反,进展似乎与系统性疾病相关。对于这种表现应进行仔细的全身评估以排除MM,因为这需要不同的管理且预后不同。