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Cervical Ganglioneuroma in Pediatric Age: A Case Report

dc.contributor.authorLima, AF
dc.contributor.authorMoreira, FC
dc.contributor.authorMenezes, A
dc.contributor.authorDias, L
dc.date.accessioned2019-03-01T14:22:10Z
dc.date.available2019-03-01T14:22:10Z
dc.date.issued2018-12
dc.description.abstractGanglioneuroma is a rare, benign, non-invasive tumor emerging from the sympathetic system. Of these tumors, only 8% occur in the neck. In this report, we present a case of a 13-year-old girl with a 2-year history of enlarging neck mass. Her only complaint, aside from neck swelling, was dysphagia. Physical and radiological examinations revealed a large mass centered in the right carotid space. A transcervical approach was used to excise the tumor emerging from the sympathetic ganglia. The patient developed temporary Horner's syndrome postoperatively. In a few weeks, she was completely asymptomatic. Histological examination was compatible with ganglioneuroma. Surgical excision is the only definite treatment of cervical ganglioneuroma and is also the only way to confirm the diagnosis. Injury during surgery may result in significant morbidity.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationTurk Arch Otorhinolaryngol. 2018 Dec;56(4):237-240.pt_PT
dc.identifier.doi10.5152/tao.2018.3690pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.23/1318
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectCriançapt_PT
dc.subjectGanglioneuromapt_PT
dc.subjectNeoplasias da Cabeça e do Pescoçopt_PT
dc.titleCervical Ganglioneuroma in Pediatric Age: A Case Reportpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage240pt_PT
oaire.citation.issue4pt_PT
oaire.citation.startPage237-240pt_PT
oaire.citation.volume56pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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