Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/19240
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dc.contributor.authorSimou, N.en
dc.contributor.authorZioga, A.en
dc.contributor.authorZygouris, A.en
dc.contributor.authorPahatouridis, D.en
dc.contributor.authorCharalabopoulos, K.en
dc.contributor.authorBatistatou, A.en
dc.date.accessioned2015-11-24T18:58:04Z-
dc.date.available2015-11-24T18:58:04Z-
dc.identifier.issn1066-8969-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/19240-
dc.rightsDefault Licence-
dc.subjectCauda Equina/*pathology/surgeryen
dc.subjectHumansen
dc.subjectImmunohistochemistryen
dc.subjectMagnetic Resonance Imagingen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectMuscular Atrophy/etiologyen
dc.subjectNeurofibroma, Plexiform/metabolism/*pathology/surgeryen
dc.subjectPeripheral Nervous System Neoplasms/metabolism/*pathology/surgeryen
dc.subjectPoliomyelitis/complications/pathologyen
dc.subjectSensation Disorders/etiologyen
dc.titlePlexiform neurofibroma of the cauda equina: a case report and review of the literatureen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1177/1066896907304521-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/18203792-
heal.identifier.secondaryhttp://ijs.sagepub.com/content/16/1/78.full.pdf-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2008-
heal.abstractPlexiform neurofibroma of the cauda equina is extremely rare. Herein, a case is reported in a 56-year-old man who also had muscle atrophy, severe motor disturbance, and mild sensory disturbance of the left leg due to childhood poliomyelitis. The clinical symptoms manifested insidiously until the patient developed cauda equina syndrome. At operation, the tumor mass was observed to engulf the nerve roots of the cauda equina. After pathological examination, the diagnosis of plexiform neurofibroma was made. Neither the patient described herein nor any previously reported patients had neurofibromatosis.en
heal.journalNameInt J Surg Patholen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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