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Title: Sunct syndrome. Report a case and treatment update
Author: Gay Escoda, Cosme
Mayor Subirana, Gemma
Camps Font, Octavi
Berini Aytés, Leonardo
Keywords: Cefalàlgia
Neuràlgia del trigemin
Malalties rares
Trigeminal neuralgia
Rare diseases
Issue Date: 1-Apr-2015
Publisher: Medicina Oral SL
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.
Note: Reproducció del document publicat a:
It is part of: Journal of Clinical and Experimental Dentistry, 2015, vol. 7, num. 2, p. e342-e347
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ISSN: 1989-5488
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Odontoestomatologia)

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