Article ID Journal Published Year Pages File Type
5627135 Clinical Neurology and Neurosurgery 2017 6 Pages PDF
Abstract

•The clinical and imaging difference between CM 1.5 and CMI is unclear.•27 CM 1.5 and 115 CM I adult patients who underwent posterior fossa decompression were evaluated.•Age at diagnosis was significantly younger in CM 1.5 group than CMI group.•The degree of tonsillar herniation was more severe in CM 1.5 group than CMI group.•Other clinical and imaging features and surgical outcomes were similar.

ObjectiveChiari malformation Type 1.5 (CM 1.5) was defined as the association of Chiari malformation Type I (CM I) and brainstem herniation. The objective was to demonstrate the difference of clinical features and surgical outcomes between CM 1.5 and CM I.Patients and methodsAll CM 1.5 and CM I adult patients who underwent posterior fossa decompression with duraplasty at our institution between 2006 and 2010 were retrospectively reviewed. Clinical characteristics, imaging features, and long-term outcomes were compared between CM 1.5 and CM I patients.ResultsA total of 142 adult patients were enrolled, including 27 CM 1.5 and 115 CM I patients. The average follow-up period was 102 months. Age at diagnosis was significantly younger in CM 1.5 group than CM I group (p = 0.039). And the degree of tonsillar herniation was significantly more severe in CM 1.5 group than CM I group (p < 0.001). There was no significant difference in other clinical and imaging characteristics. Moreover, improvement of symptoms was observed in 21 CM 1.5 patients (77.8%) and 94 CM I patients (81.7%), and no significant difference was detected (p = 0.637). There was no significant difference in the resolution of syringomyelia between CM 1.5 (72.7%) and CM I (76.5%) patients, either (p = 0. 710).ConclusionsAlthough CM 1.5 patients presented with brainstem herniation and more severe tonsillar herniation, other clinical and imaging features and surgical outcomes were similar with CM I patients. We think CM 1.5 is just a subtype of CM I, rather than a unique type of Chiari malformations.

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