Higurashi Masakazu, Yagishita Saburuo, Fujitsu Kazuhiko, Kitsuta Youichi, Takemoto Yasunori, Osano Seiki
Department of Neurosurgery, National Medical Center of Yokohama, Japan.
Brain Tumor Pathol. 2004;21(3):135-41. doi: 10.1007/BF02482189.
Plasma cell myeloma (PCM) of the skull base is rarely encountered in neurosurgical practice. PCM has a wide spectrum of pathology, including a quite benign, solitary plasmacytoma (SPC), and an extremely malignant, multiple myeloma (MM) at the two ends of the spectrum. We have described two patients with PCM of the skull base, of which one harbored SPC, and the other progressed to MM. In case 1, a 46-year-old man presented with left multiple cranial nerve impairments and had a large skull base tumor. Subtotal removal was performed. The specimen and general examination, including bone marrow aspiration, revealed SPC. Postoperatively 50Gy of external radiotherapy was administered. The patient has no manifestation of MM 24 months after the initial presentation. In case 2, a 53-year-old woman presented with left abducens palsy and had a left petroclival osteolytic mass. Gross total resection was performed. The specimen revealed a plasmablastic tumor, i.e., myeloma. General examination established the diagnosis of MM. She was administrated adjuvant chemotherapy and autologous bone marrow transplantation. She is alive without local recurrence 30 months after the initial presentation.
颅底浆细胞骨髓瘤(PCM)在神经外科实践中很少见。PCM有广泛的病理类型,包括处于该谱系两端的相当良性的孤立性浆细胞瘤(SPC)和极其恶性的多发性骨髓瘤(MM)。我们描述了两名颅底PCM患者,其中一名患有SPC,另一名进展为MM。病例1,一名46岁男性,表现为左侧多组颅神经损害,并有一个巨大的颅底肿瘤。进行了次全切除。标本及包括骨髓穿刺在内的全身检查显示为SPC。术后给予50Gy的外照射放疗。患者在初次就诊后24个月无MM表现。病例2,一名53岁女性,表现为左侧展神经麻痹,并有左侧岩斜区溶骨性肿块。进行了全切除。标本显示为浆母细胞瘤,即骨髓瘤。全身检查确诊为MM。她接受了辅助化疗和自体骨髓移植。她在初次就诊后30个月存活,无局部复发。