Prilipko O, Dehdashti A R, Zaim S, Seeck M
Presurgical Epilepsy Evaluation Unit, Program of Functional Neurology and Neurosurgery, University of Lausanne, Switzerland.
J Neurol Neurosurg Psychiatry. 2005 Jul;76(7):1034-6. doi: 10.1136/jnnp.2004.048330.
The Chiari type I malformation (CM1) is characterized by herniation of cerebellar tonsils to at least 3-5 mm below the plane of foramen magnum and can present with a wide variety of clinical symptoms, frequently including occipital headaches, secondary to bulbar and/or medullary distress. Rarely, syncopal episodes have also been described and attributed to either compression of the midbrain ascending reticular system, or vascular compromise (vertebrobasilar artery compression, hypotension). We report the first case of a CM1 patient with frequently recurring syncope due to postural orthostatic tachycardia syndrome (POTS), a form of orthostatic intolerance, whose symptoms resolved completely after surgical intervention. It is important to stress that it is not clear whether the described association of POTS and CM1 in our patient is a fortuitous finding in an isolated case or a reflection of a more systematic association between the two pathologies.
Chiari I型畸形(CM1)的特征是小脑扁桃体疝至枕骨大孔平面以下至少3 - 5毫米,可出现多种临床症状,常见的包括枕部头痛,继发于延髓和/或延髓受压。很少有晕厥发作的描述,其原因要么是中脑上行网状系统受压,要么是血管受损(椎基底动脉受压、低血压)。我们报告了首例因体位性直立性心动过速综合征(POTS)(一种直立不耐受形式)而频繁复发晕厥的CM1患者,其症状在手术干预后完全缓解。需要强调的是,目前尚不清楚我们患者中所描述的POTS与CM1之间的关联是孤立病例中的偶然发现,还是这两种病理之间更系统性关联的反映。