Furuya K, Sano K, Segawa H, Ide K, Yoneyama H
Department of Neurosurgery, Fuji Brain Institute and Hospital, Fujinomiya City, Shizuoka Prefecture, Japan.
J Neurol Neurosurg Psychiatry. 1998 Feb;64(2):221-6. doi: 10.1136/jnnp.64.2.221.
To determine if slight descent of the cerebellar tonsils (< 5 mm below the foramen magnum; tonsillar ectopia) may cause surgically treatable symptomatology.
A consecutive series of nine symptomatic patients with tonsillar ectopia seen between December 1990 and March 1993 are reported on. The same number of age and sex matched controls were selected at random from outpatients. Twelve asymptomatic subjects with tonsillar ectopia were found among 5000 people between January 1991 and March 1996. Diagnosis of tonsillar ectopia was based on midsagittal MRI.
Patients presented mainly with chronic intractable occipital dull pain, vertigo, and dysequilibrium. In all patients MRI showed normal brain structure except for tonsillar ectopia (-2.9 (SD 0.8) mm), which has historically been thought to be of no clinical relevance. In the control group the tonsilar position was +2.1 (SD 2.8) mm (p<0.01). Neurotologically abnormal findings were detected with a monaural speech integration test (100%), eye tracking test (56%), optokinetic nystagmus test (89%), and visual suppression test (67%) which strongly suggested a CNS lesion. In accordance with the results of MRI and precise neurotological examination, posterior fossa decompression surgery was carried out, followed by improvement of preoperative symptoms and less severity of neurotological abnormalities in all patients.
Tonsillar ectopia could cause neurological symptoms in small populations, which were surgically treatable. Neurotological assessment was necessary to verify the aetiological relation between tonsillar ectopia and various symptoms.
确定小脑扁桃体轻度下移(低于枕大孔5毫米以下;扁桃体异位)是否会导致可通过手术治疗的症状。
报告了1990年12月至1993年3月间连续收治的9例有症状的扁桃体异位患者。从门诊患者中随机选取了相同数量的年龄和性别匹配的对照。在1991年1月至1996年3月间的5000人中发现了12例无症状的扁桃体异位患者。扁桃体异位的诊断基于矢状位MRI。
患者主要表现为慢性顽固性枕部钝痛、眩晕和平衡失调。所有患者的MRI显示除扁桃体异位(-2.9(标准差0.8)毫米)外脑结构正常,而扁桃体异位在历史上一直被认为无临床意义。对照组扁桃体位置为+2.1(标准差2.8)毫米(p<0.01)。通过单耳言语整合测试(100%)、眼跟踪测试(56%)、视动性眼震测试(89%)和视觉抑制测试(67%)检测到神经学异常发现,强烈提示中枢神经系统病变。根据MRI结果和精确的神经学检查,进行了后颅窝减压手术,随后所有患者术前症状均有改善,神经学异常的严重程度减轻。
扁桃体异位可在少数人群中引起神经症状,这些症状可通过手术治疗。神经学评估对于验证扁桃体异位与各种症状之间的病因关系是必要的。