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dc.contributor.authorUrdániga-Hung, Mónica*
dc.contributor.authorLuza-Dueñas, Anais Casandra*
dc.contributor.authorChipana-Sotomayor, Marco Enrique*
dc.date.accessioned2017-10-20T20:20:23Z
dc.date.available2017-10-20T20:20:23Z
dc.date.issued2017-06
dc.identifier.citationNeurinoma del acústico bilateral como diagnóstico de neurofibromatosis tipo 2: reporte de caso clínico 2017 Neurología Argentinaes
dc.identifier.issn18530028
dc.identifier.doi10.1016/j.neuarg.2017.03.002
dc.identifier.urihttp://hdl.handle.net/10757/622268
dc.descriptionEl texto completo de este trabajo no está disponible en el Repositorio Académico UPC por restricciones de la casa editorial donde ha sido publicado.es_PE
dc.description.abstractNeurofibromatosis type 2 (NF2) is an autosomal dominant genetic disease that is characterized by the presence of bilateral schwannomas, meningiomas and gliomas. This is a case report of a woman of 34 years who has bilateral hipoacusia, left facial paralysis and consciousness loss in who it has been realized magnetic resonance imaging (MRI) and it has been found two mases scavenging contrast in the angle pontocerebellar. It has been established NF2 as presumptive diagnostic by diagnostic criteria. The bigger lesion was resected surgically and it has been obtained histopathologic specimens that showed acoustic schwannomas.Conclusion: The findings of MRI can be used as diagnostic method.
dc.formatapplication/pdfes
dc.language.isospaes
dc.publisherEdiciones Doyma, S.L.es
dc.relation.urlhttp://linkinghub.elsevier.com/retrieve/pii/S1853002817300253es
dc.rightsinfo:eu-repo/semantics/restrictedAccesses
dc.subjectAutosomal dominantes
dc.subjectNeurilemmomaes
dc.subjectNeurofibromatosis 2es
dc.titleNeurinoma del acústico bilateral como diagnóstico de neurofibromatosis tipo 2: reporte de caso clínicoes
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.journalNeurología Argentinaes
dc.description.peerreviewRevisión de pareses_PE
dc.contributor.emailanais.cld.102@gmail.comes_PE
refterms.dateFOA2018-06-17T05:05:28Z
html.description.abstractNeurofibromatosis type 2 (NF2) is an autosomal dominant genetic disease that is characterized by the presence of bilateral schwannomas, meningiomas and gliomas. This is a case report of a woman of 34 years who has bilateral hipoacusia, left facial paralysis and consciousness loss in who it has been realized magnetic resonance imaging (MRI) and it has been found two mases scavenging contrast in the angle pontocerebellar. It has been established NF2 as presumptive diagnostic by diagnostic criteria. The bigger lesion was resected surgically and it has been obtained histopathologic specimens that showed acoustic schwannomas.Conclusion: The findings of MRI can be used as diagnostic method.


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