Symptomatic palatal tremor: A descriptive cohort study of 27 cases in a tertiary hospital

被引:0
|
作者
Ruiz-Sandoval, Jose L. [1 ,2 ]
Chiquete-Anaya, Erwin [3 ]
Lopez-Valencia, German [1 ]
Gonzalez-Lara, Arturo [1 ]
Andrade-Ramos, Miguel A. [4 ]
Macias-Reyes, Hector [5 ]
Jimenez-Ruiz, Amado [3 ]
Rosas-Razo, Brianda [5 ]
机构
[1] Hosp Civil Guadalajara Fray Antonio Alcalde, Dept Neurol, Guadalajara, Jalisco, Mexico
[2] Univ Guadalajara, Ctr Univ Ciencias Salud CUCS, Traslat Neurosci Inst, Dept Neurosci, Guadalajara, Jalisco, Mexico
[3] Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Neurol, Mexico City, DF, Mexico
[4] Hosp Civil Guadalajara Fray Antonio Alcalde, Dept Neurosurg, Guadalajara, Jalisco, Mexico
[5] Hosp Civil Guadalajara Fray Antonio Alcalde, Dept Otorhinolaryngol, Guadalajara, Jalisco, Mexico
来源
REVISTA MEXICANA DE NEUROCIENCIA | 2020年 / 21卷 / 05期
关键词
Dysarthria; Guillain-Mollaret triangle; Hyperkinetic movement disorders; Palatal tremor; Rhomboencephalic syndrome;
D O I
10.24875/RMN.20000019
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Symptomatic palatal tremor (SPT) is an uncommon hyperkinetic movement disorder caused by the interruption of the dentato-rubro- olivary pathway due to a lesion in the brainstem or cerebellum. Methods: We describe a cohort of consecutive patients with SPT who were assessed by a single neurologist in a tertiary reference center. Results: A total of 27 patients were included in this cohort from 1998 to 2016; 16 males and 11 females, with a mean age of 47 years (range 19-89). The average time from initial insult to a diagnosis of SPT was 14.5 months (range 2-48 months). The most common etiology of SPT was cerebrovascular disease (CVD) in 21 (78%) patients. Other etiologies included infectious and demyelinating diseases of the central nervous system. The remaining unclassified case was accompanied by progressive ataxia pointing toward a neurodegenerative etiology. Twenty-six patients had a history of posterior fossa injury, and all patients had rhombencephalic signs with severe dysarthria. None of them responded significantly to pharmacological treatment. Conclusion: SPT is a more common finding than expected, especially in patients with posterior fossa injury secondary to CVD. The main clinical syndrome was the rhomboencephalic phenotype, with a predominance of dysarthria. There was no effective treatment in any of the patients.
引用
收藏
页码:199 / 204
页数:6
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