Makino K, Takamura H, Gotoh S, Andoh M
Department of Neurosurgery, Asahikawa Red Cross Hospital, Japan.
No To Shinkei. 1995 Aug;47(8):783-7.
Spinal cavernous hemangioma is rare, and it is extremely rare for cavernous hemangioma to develop in the cauda equina. There has been only one report of hydrocephalus associated with cavernous hemangioma in the cauda equina. We report a case of cavernous hemangioma in the cauda equina diagnosed on the basis of the headaches due to hydrocephalus. A 67-year-old man was being treated for Parkinson's disease because of tremor of both upper extremities for several years. In December 1991 he complained of occasional headaches. On February 15, 1992 the headaches became severe and frequent, with nausea and vomiting, and his gait became unsteady. Four days later he came to our hospital. Neurological examination revealed fine finger tremor and truncal ataxia. Computerized tomography scanning and magnetic resonance imaging of the head revealed ventricular enlargement, but there were no mass lesions obstructing the cerebrospinal fluid pathway. Lumbar puncture at the L3-L4 level yielded bloody cerebrospinal fluid, and the pressure had increased to 410 mmH2O. Cerebral angiography showed no abnormal findings. Magnetic resonance imaging of the lumbar spine demonstrated an intradural tumor at the level of vertebral body L2. Spinal angiography showed no evidence of abnormal vascularity in the mass at the L2 level. On March 10, 1992, laminectomy at three levels, L1 to L3 was performed, and a well-defined blueberry-like intra-cauda equina tumor 1 cm. in diameter, was removed. One spinal nerve root passed through the tumor. The pathological diagnosis was cavernous hemangioma. After removal of the tumor, the patient's headaches improved, and a follow-up computerized tomography scan six months later showed normal ventricle size.(ABSTRACT TRUNCATED AT 250 WORDS)
脊髓海绵状血管瘤很罕见,而在马尾发生海绵状血管瘤则极为罕见。仅有一篇关于马尾海绵状血管瘤伴发脑积水的报道。我们报告一例因脑积水导致头痛而确诊的马尾海绵状血管瘤病例。一名67岁男性因双上肢震颤患有帕金森病多年。1991年12月,他偶尔感到头痛。1992年2月15日,头痛变得严重且频繁,伴有恶心和呕吐,步态也变得不稳。四天后他来到我院。神经系统检查发现有细微的手指震颤和躯干共济失调。头颅计算机断层扫描和磁共振成像显示脑室扩大,但没有阻塞脑脊液通路的占位性病变。在L3 - L4水平进行腰椎穿刺,脑脊液呈血性,压力升至410 mmH2O。脑血管造影未见异常。腰椎磁共振成像显示L2椎体水平有硬膜内肿瘤。脊髓血管造影显示L2水平肿块处无异常血管迹象。1992年3月10日,进行了L1至L3三个节段的椎板切除术,切除了一个界限清楚、直径1厘米、类似蓝莓的马尾内肿瘤。一根脊神经根穿过肿瘤。病理诊断为海绵状血管瘤。肿瘤切除后,患者头痛症状改善,六个月后的随访计算机断层扫描显示脑室大小正常。(摘要截选至250字)