Chiari type I presenting as left glossopharyngeal neuralgia with cardiac syncope

Chiari type I presenting as left glossopharyngeal neuralgia with cardiac syncope

Autor Aguiar, P. H. Google Scholar
Tella, O. I. Google Scholar
Pereira, C. U. Google Scholar
Godinho, F. Google Scholar
Simm, R. Google Scholar
Instituição Universidade Federal de São Paulo (UNIFESP)
Fed Univ Sergipe
Neurol & Neurosurg Clin Pinheiros
Resumo Glossopharyngeal neuralgia is an uncommon craniofacial pain syndrome that is occasionally associated with cardiac syncope. However, we relate Chiari I syndrome as a cause of this clinical picture for the first time in the literature. the authors analyze the relevant literature and discuss the pathogenesis and treatment of associated syndromes. We describe the case of a 45-year-old female patient who presented with a 3-year history of left glossopharyngeal neuralgia with occasional dysphagia and episodes of syncope when eating or swallowing. the pain was not disseminated to the right side and was fairly well controlled by carbamazepine. the syncopal attacks had a duration of about 10 sec. Neurological examination elicited a faint dysphonia associated with paradoxical dysphagia. the cranial magnetic resonance imaging scan showed a bilateral herniation of the cerebellar tonsils through the foramen magnum, more evidently, on the left side. the patient received a suboccipital craniectomy and resection of the posterior arch of C L the dura mater was opened, and we found both tonsils displaced into the foramen magnum extending caudally toward the C1 level. Both tonsils were compressing the brainstem and especially the low cranial nerves bilaterally. the lower cranial nerves were compressed between the posterior inferior cerebellar artery (PICA) and the herniated cerebellar tonsil on both sides. Both PICAs were dissected by microsurgical technique and all the arachnoid adherences were cut. the left tonsil was resected by means of ultrasonic aspirator. Duraplasty was performed with the occipital pericranium. the paroxysmal pain attacks and the syncopal picture disappeared immediately after the operation. the patient was discharged on the 7th postoperative day. One year later, she was free of symptoms. This case provides clinical evidence of close connections between the glossopharyngeal and vagus nerves, which control visceral sensation; and compression of the IX and X nerves between the herniated tonsil and PICA or vertebral artery may cause an irritative sensory phenomenon, which is the origin of the algic sensation and the cardiac syncope by means of cross talk between the fibers of the same nerve.
Palavra-chave glossopharyngeal pain
cardiac syncope
Chiari I malformation
vagoglossopharyngeal neuralgia
Idioma Inglês
Data de publicação 2002-03-01
Publicado em Neurosurgical Review. New York: Springer-verlag, v. 25, n. 1-2, p. 99-102, 2002.
ISSN 0344-5607 (Sherpa/Romeo, fator de impacto)
Publicador Springer
Extensão 99-102
Fonte http://dx.doi.org/10.1007/s101430100178
Direito de acesso Acesso restrito
Tipo Artigo
Web of Science WOS:000174544400013
Endereço permanente http://repositorio.unifesp.br/handle/11600/26767

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