Kashiwazaki Daina, Hida Kazutoshi, Yano Shunsuke, Seki Toshitaka, Iwasaki Yoshinobu
Department of Neurosurgery, Hokkaido University, Graduate School of Medicine, Sapporo, Japan.
Neurosurgery. 2007 Dec;61(6):E1336-7; discussion E1337. doi: 10.1227/01.neu.0000306116.93291.94.
Hemangiopericytomas, vascular tumors arising in soft tissue, are relatively rare in the central nervous system; they comprise less than 1% of all hemangiopericytomas. Central nervous system hemangiopericytomas occur primarily in the epidural space of the brain and spinal cord. There are no previous reports of subpial, extramedullary growing central nervous system hemangiopericytomas.
We document the first case of a subpial hemangiopericytoma with extramedullary growth in the thoracic spine. The patient was a 31-year-old man who developed progressively worsening left lower limb numbness that was followed by gait disturbance over the course of 4 months.
Magnetic resonance imaging revealed an intradural tumor at the T4-T6 level of the thoracic spine. Because the patient's symptoms progressed, he underwent resection of the tumor, which had arisen in the spinal cord subpially without attachment to the dura mater.
The pathological diagnosis was hemangiopericytoma. Differential diagnoses include hemangioblastoma, meningioma, schwannoma, and solitary fibrous tumor, the clinical course and prognosis of which are different from hemangiopericytoma. Our experience indicates that hemangiopericytomas can occur as intradural tumors arising from the subpial portion.
血管外皮细胞瘤是起源于软组织的血管肿瘤,在中枢神经系统中相对罕见;它们占所有血管外皮细胞瘤的比例不到1%。中枢神经系统血管外皮细胞瘤主要发生在脑和脊髓的硬膜外间隙。此前尚无关于软膜下、髓外生长的中枢神经系统血管外皮细胞瘤的报道。
我们记录了首例胸椎软膜下髓外生长的血管外皮细胞瘤病例。患者为一名31岁男性,在4个月的病程中逐渐出现左下肢麻木加重,随后出现步态障碍。
磁共振成像显示胸椎T4-T6水平硬膜内有肿瘤。由于患者症状进展,他接受了肿瘤切除术,该肿瘤起源于脊髓软膜下,未附着于硬脑膜。
病理诊断为血管外皮细胞瘤。鉴别诊断包括血管母细胞瘤、脑膜瘤、神经鞘瘤和孤立性纤维瘤,其临床病程和预后与血管外皮细胞瘤不同。我们的经验表明,血管外皮细胞瘤可作为起源于软膜部分的硬膜内肿瘤发生。