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Sunct syndrome. Report of a case and treatment update

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Sunct syndrome. Report of a case and treatment update

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dc.contributor.author Gay Escoda, Cosme es
dc.contributor.author Mayor Subirana, Gemma es
dc.contributor.author Camps Font, Octavi es
dc.contributor.author Berini Aytés, Leonardo es
dc.date.accessioned 2015-06-29T11:48:16Z
dc.date.available 2015-06-29T11:48:16Z
dc.date.issued 2015 es
dc.identifier.citation Gay Escoda, Cosme ; Mayor Subirana, Gemma ; Camps Font, Octavi ; Berini Aytés, Leonardo. Sunct syndrome. Report of a case and treatment update. En: Journal of Clinical and Experimental Dentistry, 2015, Vol. 7, No. 2: 342-347 es
dc.identifier.uri http://hdl.handle.net/10550/44861
dc.description.abstract Short-lasting unilateral neuralgiform headache attacks with conjuntival injection and tearing (SUNCT) is considered a rare trigeminal autonomic cephalgias, a group of primary headache disorders characterized by brief episodes of severe unilateral headache in the distribution territory of the trigeminal nerve, accompanied by prominent ipsilateral and cranial parasympathetic autonomic features. The present report describes a SUNCT syndrome in a 64-year-old male who had been diagnosed with trigeminal neuralgia several years ago. The patient reported stabbing pain in the orbital zone and in the left upper maxillary region, of great intensity, brief duration, and a frequency of 20-100 attacks a day. Pain episodes were accompanied by conjunctival injection and tearing. Based on the anamnesis, clinical examination and a magnetic resonance imaging scan, episodic SUNCT syndrome was diagnosed and pharmacological treatment with topiramate was started. This reduced the intensity and number of attacks to 3-6 a day en_US
dc.subject Odontología es
dc.subject Ciencias de la salud es
dc.title Sunct syndrome. Report of a case and treatment update es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.type.hasVersion VoR es_ES

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