Sato M, Saito T, Yamaguchi K
Department of Neurosurgery, Ohta Nishinouti Hospital, Koriyama, Japan.
No Shinkei Geka. 1993 Nov;21(11):1061-4.
A rare case of primary malignant lymphoma of the skull presenting a huge mass lesion is reported. A 65-year-old male was admitted complaining of a huge scalp mass (largest 13 x 9 x 4 cm) which was growing rapidly. On admission he showed hemiparesis. The craniogram revealed a large osteolytic lesion of the right parietal bone. Computed tomography and magnetic resonance images revealed a huge tumoral mass lesion expanding from the epidural to the subcutaneous space at the frontoparietal region. The angiogram showed marked tumor stain feeding from the bilateral middle meningeal artery and the superficial temporal artery. On operation, the tumor was shown to be elastic soft, and existed in the epidural and subcutaneous space. It was invading the diploic, with infiltration into the dura. The tumor was detached from the dura matter and totally resected. The histological diagnosis was malignant lymphoma (B cell type). After the operation, the patient's left hemiparesis improved without additional neurological deficit. Bone and tumor scintigraphy disclosed no uptake other than that of the head. The tumor was diagnosed at primary malignant lymphoma of the skull. After 50-Gy radiation and chemotherapy, the postoperative course was uneventful. Although the number of reports on malignant lymphoma has increased recently, there are only 15 case reports concerning those in the skull. The neuroradiological findings and differential diagnosis of malignant lymphoma in the skull were mainly discussed.
报告了一例罕见的原发性颅骨恶性淋巴瘤,表现为巨大肿块病变。一名65岁男性因主诉巨大头皮肿块(最大13×9×4厘米)且生长迅速而入院。入院时他出现偏瘫。颅骨X线片显示右顶骨有一个大的溶骨性病变。计算机断层扫描和磁共振成像显示,额顶部区域有一个巨大的肿瘤性肿块病变,从硬膜外扩展至皮下间隙。血管造影显示有明显的肿瘤染色,由双侧脑膜中动脉和颞浅动脉供血。手术中发现肿瘤质地弹性柔软,存在于硬膜外和皮下间隙,侵犯板障并浸润硬膜。肿瘤从硬膜上分离并完全切除。组织学诊断为恶性淋巴瘤(B细胞型)。术后患者左侧偏瘫改善,无额外神经功能缺损。骨和肿瘤闪烁扫描显示除头部外无其他摄取。该肿瘤被诊断为原发性颅骨恶性淋巴瘤。经过50 Gy的放疗和化疗后,术后过程顺利。尽管最近关于恶性淋巴瘤的报道有所增加,但关于颅骨恶性淋巴瘤的病例报告仅有15例。主要讨论了颅骨恶性淋巴瘤的神经放射学表现及鉴别诊断。