Nishimura T, Uchida Y, Fukuoka M, Ono Y, Kurisaka M, Mori K
Kochi Cerebrovascular Research Institute, Uchida Neurosurgery Clinic, Kochi-City, Japan.
Surg Neurol. 1998 Nov;50(5):480-5; discussion 485-6. doi: 10.1016/s0090-3019(97)00362-5.
Although malignant lymphomas of the central nervous system have been reported to be increasing in frequency, cerebellopontine (CP) angle lymphoma is rare and only 13 cases have been reported previously in the literature.
A 63-year-old woman had progressive dizziness and nausea for 2 months. Computed tomography scanning and magnetic resonance imaging (MRI) revealed a mass lesion in the left CP angle, that was compressing the lateral-dorsal aspect of the pons and the fourth ventricle. This tumor was avascular on angiography. The tumor was surgically removed through a left lateral suboccipital approach. It was considered to arise from the subarachnoid space of the CP angle cistern. For some reason, the histologic diagnosis was not definitively made, and therefore radiation therapy was not planned. The tumor recurred within 50 days after the tumor excision. Surgical excision of the recurrent tumor was performed again. The histologic diagnosis was B-cell type malignant lymphoma. Radiation therapy was performed. In the 27 months since irradiation, a recurrent tumor has not been detected on MRI.
Although erosion and expansion of the internal auditory canal suggest an acoustic neurinoma, CP angle lymphoma can, in rare circumstances, erode the internal auditory canal. There are three distinct patterns in which malignant lymphomas occupy the CP angle: (1) an extra-axial CP angle lymphoma, (2) an intra-axial lymphoma extending to the CP angle, and (3) a leptomeningeal lymphoma presenting as a CP angle lesion. Although malignant lymphomas rarely occupy the CP angle, it should be considered in the differential diagnosis of CP angle tumors. It is desirable to obtain a frozen section in all CP angle tumors during surgery to identify the tumor, because aggressive removal is not necessary, but radiation therapy should additionally be performed for malignant lymphomas.
尽管中枢神经系统恶性淋巴瘤的发病率据报道呈上升趋势,但桥小脑角(CP)淋巴瘤却很罕见,此前文献中仅报道过13例。
一名63岁女性出现进行性头晕和恶心2个月。计算机断层扫描和磁共振成像(MRI)显示左侧桥小脑角有一肿块病变,压迫脑桥背外侧和第四脑室。血管造影显示该肿瘤无血管。通过左侧枕下外侧入路手术切除肿瘤。考虑肿瘤起源于桥小脑角池蛛网膜下腔。由于某些原因,未明确做出组织学诊断,因此未计划进行放射治疗。肿瘤切除后50天内复发。再次对复发性肿瘤进行手术切除。组织学诊断为B细胞型恶性淋巴瘤。进行了放射治疗。放疗后的27个月里,MRI未检测到复发性肿瘤。
尽管内耳道侵蚀和扩大提示听神经瘤,但在罕见情况下,桥小脑角淋巴瘤也可侵蚀内耳道。恶性淋巴瘤占据桥小脑角有三种不同模式:(1)轴外桥小脑角淋巴瘤;(2)延伸至桥小脑角的轴内淋巴瘤;(3)表现为桥小脑角病变的柔脑膜淋巴瘤。尽管恶性淋巴瘤很少占据桥小脑角,但在桥小脑角肿瘤的鉴别诊断中应予以考虑。手术中对所有桥小脑角肿瘤进行冷冻切片检查以明确肿瘤类型是可取的,因为对于恶性淋巴瘤不必进行积极切除,但应额外进行放射治疗。