Oishi Tomoya, Sakai Naoto, Sameshima Tetsuro, Kawaji Hiroshi, Namba Hiroki
Department of Neurosurgery, Hamamatsu University School of Medicine, Handayama 1-20-1, Higashiku, Hamamatsu, Shizuoka, 431-3192, Japan.
J Med Case Rep. 2017 Mar 9;11(1):63. doi: 10.1186/s13256-017-1220-8.
Intradural extramedullary cavernous angiomas of the central nervous system are a rare type of cavernous angioma, but they can cause fatal subarachnoid hemorrhage. The efficacy of resection for this type of cavernous malformations remains uncertain. This is the first report to recommend surgical resection of these types of lesions regardless of the fatal condition.
Our patient was a 70-year-old Japanese man who experienced a sudden onset of an occipital headache, followed by bilateral abducens nerve palsy. Magnetic resonance imaging revealed a small amount of hemorrhage in both of the lateral ventricles and an intradural extramedullary mass lesion in the left side of his foramen magnum. Two weeks after the appearance of initial symptoms, he became comatose. A computed tomography scan showed an increase in the subarachnoid intraventricular hemorrhaging and of the acute hydrocephalus. Following ventricular drainage, total tumor resection was performed using the lateral suboccipital transcondylar approach in conjunction with a first cervical hemilaminectomy. We observed a grape-like vascular-rich tumor with calcification that was adhering tightly to the wall of his left vertebral artery. A histopathological examination of the surgery specimen identified it as a cavernous angioma. After placement of a ventriculoperitoneal shunt and 2 months of rehabilitation, he recovered completely.
An intradural extramedullary foramen magnum cavernous malformation is quite rare. The fragile surface of our patient's lesion was causing repeated subarachnoid hemorrhage and consequently progressive fatal neurological deterioration. Surgical resection of the lesion to prevent repeated hemorrhage was performed and he recovered fully. Therefore, we recommend surgical resection of the lesion regardless of the potentially fatal condition.
中枢神经系统硬膜内髓外海绵状血管瘤是一种罕见的海绵状血管瘤类型,但可导致致命的蛛网膜下腔出血。这类海绵状畸形的切除疗效仍不确定。本文是首例建议对这类病变进行手术切除的报告,无论病情是否危急。
我们的患者是一名70岁的日本男性,突发枕部头痛,随后出现双侧展神经麻痹。磁共振成像显示双侧侧脑室少量出血,枕骨大孔左侧有硬膜内髓外肿块病变。初始症状出现两周后,患者昏迷。计算机断层扫描显示蛛网膜下腔和脑室内出血增加以及急性脑积水。在进行脑室引流后,采用枕下外侧经髁入路联合第一颈椎半椎板切除术进行了肿瘤全切。我们观察到一个葡萄状、富含血管且有钙化的肿瘤,它紧紧附着于左侧椎动脉壁。手术标本的组织病理学检查确定其为海绵状血管瘤。在置入脑室腹腔分流管并经过2个月的康复治疗后,他完全康复。
枕骨大孔硬膜内髓外海绵状畸形非常罕见。我们患者病变的脆弱表面导致反复蛛网膜下腔出血,进而导致进行性致命性神经功能恶化。为防止反复出血,对病变进行了手术切除,患者完全康复。因此,我们建议对该病变进行手术切除,无论病情是否危急。