Department of Neurosurgery, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
Department of Neurosurgery, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
World Neurosurg. 2019 Aug;128:415-421. doi: 10.1016/j.wneu.2019.05.034. Epub 2019 May 22.
Extra-axial cavernoma (EAC) at the cerebellopontine angle (CPA) is a rare clinical entity that can mimic radiologically several lesions encountered at this location. We report a case of EAC-CPA and present a review of the literature.
A PubMed research was conducted looking for EAC-CPA lesions described in literature. After reviewing all the relevant articles, the following data were extracted and organized into a single table: patients' symptoms, radiological characteristics, surgical procedure, histopathology, and outcome.
Eighteen cases (including ours) were identified from these reports. Mean age at diagnosis was 42 with a male:female ratio of 2.6:1. The most commonly involved cranial nerves were the vestibulocochlear complex followed by the trigeminal nerve. The lesions were iso-to hypodense on computed tomography. On magnetic resonance imaging, the EAC-CPA can be solid or cystic. All lesions were approached using retrosigmoid craniotomies. Histologically, both intra- and extra-axial cavernomas are identical, consisting of devoid vascular sinusoids with endothelial lining. The outcome was favorable in 16/18 of the described cases. One case presented a worsened facial paresis and 1 patient died from excessive intraoperative bleeding and subsequent complications.
Despite the fact that EAC-CPA are rarely encountered, it should be kept in mind in the list of differential diagnosis, preparing both the surgeon and anesthesiologist for the surgery of a vascular lesion. Specific radiological features, especially an associated developmental venous anomaly could point to the diagnosis.
桥小脑角(CPA)的硬膜外海绵状血管瘤(EAC)是一种罕见的临床实体,在影像学上可以模拟出在该部位遇到的几种病变。我们报告了一例 EAC-CPA 病例,并对文献进行了回顾。
在 PubMed 上进行了研究,寻找文献中描述的 EAC-CPA 病变。在回顾了所有相关文章后,我们提取并组织到一个表格中以下数据:患者的症状、影像学特征、手术过程、组织病理学和结果。
从这些报告中确定了 18 例(包括我们的病例)。诊断时的平均年龄为 42 岁,男女比例为 2.6:1。最常受累的颅神经是前庭耳蜗复合体,其次是三叉神经。病变在计算机断层扫描上呈等至低密。在磁共振成像上,EAC-CPA 可以是实性或囊性的。所有病变均采用乙状窦后颅切开术进行治疗。组织学上,硬膜内和硬膜外海绵状血管瘤是相同的,由缺乏血管窦和内皮衬里组成。在描述的 18 例病例中,16 例的结果良好。1 例出现面瘫加重,1 例患者因术中过度出血和随后的并发症死亡。
尽管 EAC-CPA 很少见,但在鉴别诊断的列表中应牢记这一点,为血管病变的手术做好外科医生和麻醉师的准备。特定的影像学特征,特别是伴发的发育性静脉异常,可能提示诊断。