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Spontaneous Dissection of the Renal Artery in Vascular Ehlers-Danlos Syndrome

dc.contributor.authorPereira, F.
dc.contributor.authorCardoso, T.
dc.contributor.authorSá, P.
dc.date.accessioned2016-07-26T12:47:32Z
dc.date.available2016-07-26T12:47:32Z
dc.date.issued2015
dc.description.abstractEhlers-Danlos syndrome (EDS) is a rare heterogeneous group of connective tissue disorders. The vascular type (vEDS) is an autosomal dominant disorder caused by heterozygous mutations in the COL3A1 gene predisposing to premature arterial, intestinal, or uterine rupture. We report a case of a 38-year-old woman with a recent diagnosis of vEDS admitted in the Emergency Department with a suspicion of a pyelonephritis that evolved to a cardiopulmonary arrest. A fatal retroperitoneal hematoma related with a haemorrhagic dissection of the right renal artery was found after emergency surgery. This case highlights the need to be aware of the particular characteristics of vEDS, such as a severe vascular complication that can lead to a fatal outcome.pt_PT
dc.identifier.citationCase Rep Crit Care. 2015;2015:804252pt_PT
dc.identifier.doi10.1155/2015/804252pt_PT
dc.identifier.issn2090-6420
dc.identifier.urihttp://hdl.handle.net/10400.16/1974
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherHindawi Publishing Corporationpt_PT
dc.relation.publisherversionhttp://www.hindawi.com/journals/cricc/2015/804252/pt_PT
dc.titleSpontaneous Dissection of the Renal Artery in Vascular Ehlers-Danlos Syndromept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceUnited States of Americapt_PT
oaire.citation.startPage804252pt_PT
oaire.citation.titleCase Reports in Critical Carept_PT
oaire.citation.volume2015pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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