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Orbital apex syndrome affecting head and neck cancer patients : a case series

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Orbital apex syndrome affecting head and neck cancer patients : a case series

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dc.contributor.author Ribeiro, Ana-Carolina-Prado es
dc.contributor.author Luiz, Ana-Claudia es
dc.contributor.author Montezuma, Marco Aurelio es
dc.contributor.author Mak, Milena Perez es
dc.contributor.author Santos Silva, Alan Roger es
dc.contributor.author Brandao, Thais-Bianca es
dc.date.accessioned 2017-07-24T09:29:05Z
dc.date.available 2017-07-24T09:29:05Z
dc.date.issued 2017 es
dc.identifier.citation Ribeiro, Ana-Carolina-Prado ; Luiz, Ana-Claudia ; Montezuma, Marco Aurelio ; Mak, Milena Perez ; Santos Silva, Alan Roger ; Brandao, Thais-Bianca. Orbital apex syndrome affecting head and neck cancer patients : a case series. En: Medicina oral, patología oral y cirugía bucal. Ed. inglesa, 22 3 2017: 12- es
dc.identifier.uri http://hdl.handle.net/10550/59850
dc.description.abstract Orbital apex syndrome (OAS) is a complex and uncommon disorder that typically damages multiple cranial nerves in association with optic nerve dysfunction. OAS is associated with several different pathologies, however; only a few cases have been reported in association with head and neck cancer (HNC) so far. A case series of HNC patients diagnosed with OAS is described including clinicopathological data, image findings, and disease outcome. Ptosis and diplopia were diagnosed in four male patients with mean age of 61.2 years who were undergoing treatment for late-stage carcinomas of the tongue, larynx, and nasopharynx, eventually leading to the diagnosis of OAS. The mean overall survival rate after the diagnosis of OAS was 9.5 months. The current study reinforces evidence that OAS indicates poor prognosis and highlights the importance of early diagnosis. es
dc.title Orbital apex syndrome affecting head and neck cancer patients : a case series es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.identifier.doi 10.4317/medoral.21506 es
dc.type.hasVersion VoR es_ES

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