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dc.contributor.authorNwaorgu, OGB-
dc.contributor.authorAdoga, AS-
dc.contributor.authorOnakoya, PA-
dc.contributor.authorAdoga, A A-
dc.date.accessioned2025-05-29T13:05:26Z-
dc.date.available2025-05-29T13:05:26Z-
dc.date.issued2004-
dc.identifier.citationAfr. J. Med. Med. Sci. (2004) 33, 83-85en_US
dc.identifier.issn1116-4077-
dc.identifier.urihttp://adhlui.com.ui.edu.ng/jspui/handle/123456789/4359-
dc.descriptionArticleen_US
dc.description.abstractParagangliomas are neuroendocrine neoplasms that primarily afflict patients during the fourth- and fifth-decades of life. The majority of extra-adrenal paraganglioma s arise in the head and neck region, notably from the carotid and aortic bodies Jugular bulb and tympani c plexus. Although one-fifth of all parapharyngeal neoplasms a r e paragangliomas, primary hypopharyngeal paraganglioma is relatively uncommon, only one other case having previously been documented by Filippin et al. (1989). We report a second case of hypopharyngeal paraganglioma in an 18-year-old male as seen in our centeren_US
dc.description.sponsorshipCOLLEGE OF MEDICINE, UNIVERSITY OF IBADAN, NIGERIAen_US
dc.language.isoenen_US
dc.publisherCOLLEGE OF MEDICINE, UNIVERSITY OF IBADAN, NIGERIAen_US
dc.subjectParagangliomaen_US
dc.subjectHypopharynxen_US
dc.subjectTracheostomyen_US
dc.subjectIbadanen_US
dc.subjectNigeriaen_US
dc.titleHypopharyngeal paraganglioma: a case reporten_US
dc.typeArticleen_US
Appears in Collections:African Journal of Medicine and Medical Sciences

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