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Childs Nerv Syst ; 6(3): 126-30, 1990 May.
Artigo em Inglês | MEDLINE | ID: mdl-2192796

RESUMO

Many excellent reports have dealt with the various aspects of cranial chordoma. It remains a relatively rare neoplasm, particularly in younger children. The authors have had the opportunity to treat a 5-year-old child harboring a basiocciput chordoma. It extended from the mid-clivus to C3. A transoral labiomandibular approach was used, allowing its resection. No evidence of recurrence was noted 3 years later. A literature search confirmed the rarity of basiocciput chordoma in young children. The perioperative difficulties encountered prompted this report.


Assuntos
Cordoma/cirurgia , Osso Occipital , Neoplasias Cranianas/cirurgia , Pré-Escolar , Cordoma/diagnóstico , Cordoma/patologia , Feminino , Humanos , Lábio/cirurgia , Imageamento por Ressonância Magnética , Mandíbula/cirurgia , Boca , Neoplasias Cranianas/diagnóstico , Neoplasias Cranianas/patologia
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