Ohba Shigeo, Miwa Tomoru, Kawase Takeshi
Department of Neurosurgery, Keio University School of Medicine, Tokyo, Japan.
Neurosurgery. 2006 Apr;58(4):E791; discussion E791. doi: 10.1227/01.NEU.0000204307.99246.17.
Schwannomas originating from the trochlear nerve without neurofibromatosis are extremely rare. Thirty-four cases have previously been reported in the literature, and only 25 cases were pathologically diagnosed. In addition, intratumoral hemorrhage in intracranial schwannomas is also rare. Approximately 30 cases of intracranial schwannomas with intratumoral hemorrhage have been reported.
A 42-year-old man presented with left hemiparesis and right trochlear nerve palsy. Magnetic resonance imaging revealed an abnormal cystic lesion beside the brainstem. His symptoms rapidly worsened after enlargement of the mass because of intratumoral hemorrhage.
Gross total removal of the tumor was performed via the anterior transpetrosal approach. The tip of the trochlear nerve was fanned out and unified with the tumor. The tumor was diagnosed as a schwannoma.
The patient's hemiparesis improved postoperatively, and he was discharged 1 week after the operation. Magnetic resonance imaging performed 4 months later revealed no regrowth of the tumor. Only right trochlear nerve palsy has persisted. This report is the second case of intratumoral hemorrhage from a trochlear nerve schwannoma.
起源于滑车神经且无神经纤维瘤病的施万细胞瘤极为罕见。此前文献报道过34例,其中仅25例经病理诊断。此外,颅内施万细胞瘤内出血也很罕见。大约有30例颅内施万细胞瘤伴瘤内出血的病例被报道。
一名42岁男性出现左侧偏瘫和右侧滑车神经麻痹。磁共振成像显示脑干旁有一个异常囊性病变。由于瘤内出血导致肿块增大后,他的症状迅速恶化。
通过经岩骨前入路对肿瘤进行了全切除。滑车神经末梢呈扇形展开并与肿瘤相连。肿瘤被诊断为施万细胞瘤。
患者术后偏瘫症状改善,术后1周出院。4个月后进行的磁共振成像显示肿瘤无复发。仅右侧滑车神经麻痹持续存在。本报告是滑车神经施万细胞瘤瘤内出血的第二例病例。