Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4938
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dc.contributor.authorSwift, K.en
dc.contributor.authorBorzi, P.en
dc.date.accessioned2022-11-07T23:57:50Z-
dc.date.available2022-11-07T23:57:50Z-
dc.date.issued2020en
dc.identifier.citation16 , 2020, p. S6en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/4938-
dc.description.abstractPheochromocytoma and paraganglioma are uncommon tumours in children. There are often resectable but need lifelong surveillance due to high rate of recurrence. We present a 9 yr. old presenting with hypertensive encaphalopathy. An obstructed right kidney was found. It was secondary to a ureteric paraganglioma. This was resected and a midureteric interposition with appendix was performed successfully. We review the literature and experience with this rare tumour.L20078919512021-03-04 <br />en
dc.language.isoenen
dc.relation.ispartofJournal of Pediatric Urologyen
dc.titleUreteric paraganglioma with appendiceal interposition in a 9 yr. olden
dc.typeArticleen
dc.identifier.doi10.1016/j.jpurol.2020.05.027en
dc.subject.keywordshumanen
dc.subject.keywordsappendixconference abstracten
dc.subject.keywordskidneyen
dc.subject.keywordsparagangliomaen
dc.subject.keywordssystematic reviewen
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L2007891951&from=exporthttp://dx.doi.org/10.1016/j.jpurol.2020.05.027 |en
dc.identifier.risid1158en
dc.description.pagesS6en
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Sites:Children's Health Queensland Publications
Queensland Health Publications
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