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Coexistence of Pheochromocytoma and Renal Artery Stenosis in a Pediatric Patient with Hypertension

dc.contributor.authorSerras, I
dc.contributor.authorBaeta Baptista, R
dc.contributor.authorFrancisco, T
dc.contributor.authorCasimiro, A
dc.contributor.authorLito, D
dc.contributor.authorAlves, R
dc.contributor.authorAbranches, M
dc.date.accessioned2018-12-04T13:35:49Z
dc.date.available2018-12-04T13:35:49Z
dc.date.issued2018
dc.description.abstractPheochromocytoma and renal artery stenosis are surgically treatable causes of hypertension. Although rare, the coexistence of pheochromocytoma and renal artery stenosis has been described in case reports. Common pathophysiological mechanisms other than extrinsic compression may be involved in this association, such as catecholamine-induced vasospasm. The early recognition of the association of pheochromocytoma with renal artery stenosis is essential for appropriate treatment planning. We present the case of a previously healthy tenyear- old boy who presented with hypertensive encephalopathy, tachycardia and diaphoresis. Hypertension was found to be secondary to a catecholamine-producing tumor associated with coexisting renal artery stenosis. Hypertension resolved a few months after successful pheochromocytoma excision, without renal artery revascularization.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationPort J Nephrol Hypert 2018; 32(1): 78-82pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/3132
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSociedade Portuguesa de Nefrologiapt_PT
dc.subjectHypertensionpt_PT
dc.subjectPheochromocytomapt_PT
dc.subjectEncephalopathy Syndromept_PT
dc.subjectRenal Artery Stenosispt_PT
dc.subjectChildpt_PT
dc.subjectHDE PEDpt_PT
dc.subjectHDE NEF PEDpt_PT
dc.subjectHDE CIR PEDpt_PT
dc.subjectHDE UCI PEDpt_PT
dc.titleCoexistence of Pheochromocytoma and Renal Artery Stenosis in a Pediatric Patient with Hypertensionpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage82pt_PT
oaire.citation.issue1pt_PT
oaire.citation.startPage78pt_PT
oaire.citation.volume32pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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