Di Stasi M, Cavanna L, Paties C, Fornari F, Civardi G, Binelli F, Buscarini E, Buscarini L
Acta Haematol. 1986;76(4):202-7. doi: 10.1159/000206056.
Anaplastic myeloma represents a rare variety of multiple myeloma, with poor prognosis and no response to therapy. 56 cases reported in the literature are reviewed and one case evaluated with immunohistochemical techniques is described. This case is of special interest in the following points: the anaplastic myeloma arose in extramedullary sites in a patient with typical multiple myeloma in remission; differential histological diagnosis between anaplastic myeloma and immunoblastic lymphoma was very difficult without immunohistochemical techniques; the anaplastic phase presented an atypical neurologic feature, the Collet-Sicard syndrome, and the treatment with radio-chemotherapy (including adriamycin) did not induce any clinical improvement.
间变性骨髓瘤是多发性骨髓瘤中一种罕见的类型,预后较差且对治疗无反应。本文回顾了文献报道的56例病例,并描述了1例采用免疫组化技术评估的病例。该病例在以下方面具有特殊意义:间变性骨髓瘤发生于一名处于缓解期的典型多发性骨髓瘤患者的髓外部位;若无免疫组化技术,间变性骨髓瘤与免疫母细胞淋巴瘤的组织学鉴别诊断非常困难;间变性阶段呈现出非典型的神经学特征——科莱-西卡尔综合征,并且放化疗(包括阿霉素)治疗未带来任何临床改善。