Kanai Makoto, Kawano Kazuhiko, Murakami Tatsuya, Saitou Motoi, Kikumoto Naoki
Department of Neurosurgery, Terakata Ikuno Hospital, 1-5-10 Terakata, Hondoori, Moriguchi-city, Osaka 570-0048, Japan.
No Shinkei Geka. 2003 Apr;31(4):419-24.
We report a rare case of malignant lymphopma of the cranial vault. A 71-year-old woman developed an asymptomatic subcutaneous mass on the scalp. The skin over the lesion was normal and the mass was firm and attached to the skull. Neurological examination revealed no abnormalities. Plain CT scans showed a high-density lesion that was widely attached to the skull and the surface of the skull was slightly irregular. About 25 days later, enhanced CT showed that the mass was well enhanced and extended into the cranium, and decalcification of the skull adjacent to the lesion had progressed. MRI showed long T1 and T2 values of the mass and the adjacent bone marrow. Bone scintigraphy and gallium scintigraphy showed prominent accumulation of radioisotopes in the scalp lesion. The mass, dura, and infiltrated bone were resected, and the surface of the brain was found to be intact. Histological examination revealed that the tumor was non-Hodgkin's lymphoma (diffuse, medium-sized, B cell lymphoma). The fact that the tumor first developed extracranially and then extended into the cranium without severe bone destruction and the fact that the dura completely protected the brain surface may indicate that the malignant lymphoma originated from the skull and showed infiltrative growth, while the dura provided a strong barrier to its intracranial extension. Thus, malignant lymphoma originating from the skull may tend to extend outside the cranium first and within the cranium subsequently, as in our case, and this may be the reason why the complaint at presentation of more than half of the reported patients is a scalp mass rather than any neurological sign.
我们报告一例罕见的颅顶恶性淋巴瘤病例。一名71岁女性头皮出现无症状皮下肿块。病变上方皮肤正常,肿块质地坚硬,与颅骨相连。神经系统检查未发现异常。平扫CT扫描显示一个高密度病变,广泛附着于颅骨,颅骨表面略有不规则。约25天后,增强CT显示肿块强化良好并延伸至颅骨内,病变相邻颅骨的脱钙进展。MRI显示肿块及相邻骨髓呈长T1和T2信号。骨闪烁显像和镓闪烁显像显示头皮病变处放射性核素明显聚集。切除肿块、硬脑膜和浸润的骨质,发现脑表面完整。组织学检查显示肿瘤为非霍奇金淋巴瘤(弥漫性、中等大小、B细胞淋巴瘤)。肿瘤最初发生于颅外,然后延伸至颅内,且无严重骨质破坏,以及硬脑膜完全保护脑表面这一事实,可能表明恶性淋巴瘤起源于颅骨并呈浸润性生长,而硬脑膜对其颅内延伸构成了强大屏障。因此,如我们的病例所示,起源于颅骨的恶性淋巴瘤可能倾向于先向颅外延伸,随后向颅内延伸,这可能就是超过半数报告患者就诊时的主诉为头皮肿块而非任何神经系统症状的原因。