Kobata H, Kondo A, Iwasaki K, Nishioka T
Department of Neurosurgery, Kitano Medical Research Institute and Hospital, Osaka, Japan.
Neurosurgery. 1998 Dec;43(6):1351-61; discussion 1361-2. doi: 10.1097/00006123-199812000-00052.
A pathological condition caused by vascular compression at the root entry/exit zone of the cranial nerves is designated hyperactive dysfunction syndrome (HDS) of the cranial nerves. Patients with HDS who exhibited a combination of trigeminal neuralgia (TN), hemifacial spasm (HFS), and/or glossopharyngeal neuralgia were retrospectively reviewed, to study the incidence, etiological factors, and demographic characteristics for this combined HDS group.
Medical and surgical records were analyzed for 41 patients with combined HDS, of 1472 consecutive patients with HDS who were treated between 1984 and 1994.
The combined HDS group accounted for 2.8% of all patients with HDS; 19 patients (1.3%) exhibited bilateral symptoms, i.e., 14 cases of TN, 3 of combined TN and HFS, and 2 of HFS. Twenty-two patients (1.5%) exhibited ipsilateral symptoms, i.e., 19 cases of TN and HFS and 3 of TN and glossopharyngeal neuralgia. Excluding three patients whose symptoms were associated with brain tumors or arteriovenous malformations, this patient group was older (63.2 versus 55.3 yr, P = 0.0009) and exhibited an increased percentage of associated hypertension (47.4 versus 17.5%, P = 0.000008), with a female predominance (86.8 versus 71.3%, P = 0.07), compared with the single HDS group. Thirty-six of these patients underwent a total of 61 microvascular decompression procedures, with favorable outcomes. The offending vessels were similar to those in single HDS, which were usually conventional and multiple.
The associated etiological factors for vascular compression syndromes were more evident in the combined HDS group than in the single HDS group. Progressive arteriosclerotic vasculoarchitectural changes of the vertebrobasilar system, accelerated by aging and hypertension, bring about the development of combined HDS, with a remarkable female predominance.
由颅神经根入/出区血管受压引起的病理状态被称为颅神经功能亢进性功能障碍综合征(HDS)。对表现为三叉神经痛(TN)、半面痉挛(HFS)和/或舌咽神经痛组合的HDS患者进行回顾性研究,以探讨该合并型HDS组的发病率、病因及人口统计学特征。
分析了1984年至1994年间接受治疗的1472例连续性HDS患者中41例合并型HDS患者的医疗和手术记录。
合并型HDS组占所有HDS患者的2.8%;19例患者(1.3%)表现为双侧症状,即14例TN、3例TN合并HFS和2例HFS。22例患者(1.5%)表现为同侧症状,即19例TN合并HFS和3例TN合并舌咽神经痛。排除3例症状与脑肿瘤或动静脉畸形相关的患者后,该患者组年龄更大(63.2岁对55.3岁,P = 0.0009),合并高血压的比例更高(47.4%对17.5%,P = 0.000008),女性占主导(86.8%对71.3%,P = 0.07),与单纯HDS组相比。这些患者中有36例共接受了61次微血管减压手术,效果良好。致病血管与单纯HDS中的相似,通常是常见且多发的。
血管压迫综合征的相关病因在合并型HDS组比单纯HDS组更明显。由衰老和高血压加速的椎基底系统进行性动脉硬化血管结构改变导致了合并型HDS的发生,女性占主导明显。