A Case of Arteriovenous Malformation Presenting as Wallenberg Syndrome / 대한이비인후과학회지
Korean Journal of Otolaryngology - Head and Neck Surgery
; : 352-355, 2011.
Article
de Ko
| WPRIM
| ID: wpr-651605
Bibliothèque responsable:
WPRO
ABSTRACT
Lateral medullary syndrome, also known as Wallenberg syndrome, is characterized by sensory deficits affecting the trunk and extremities on the opposite side of the lesion, and the face and cranial nerves on the same side of the lesion. Other clinical symptoms and findings are dysphagia, slurred speech, ataxia, facial pain, vertigo with nystagmus, Horner's syndrome, diplopia, and possibly palatal myoclonus. The cause of this syndrome is usually occlusion of the posterior inferior cerebellar artery or vertebrobasillar artery. We observed a case of Wallenberg syndrome occuring secondary to the cavernous malformation and initially presenting as unilateral vocal cord palsy. The centrally-medicated vocal cord palsy is a rare cause of hoarseness, but should be considered in cases where no other local cause can be found.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Artères
/
Malformations artérioveineuses
/
Ataxie
/
Syndrome de Wallenberg
/
Algie faciale
/
Troubles de la déglutition
/
Vertige
/
Paralysie des cordes vocales
/
Enrouement
/
Syndrome de Claude Bernard-Horner
langue:
Ko
Texte intégral:
Korean Journal of Otolaryngology - Head and Neck Surgery
Année:
2011
Type:
Article