Angiokeratomas, not everything is fabry disease

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dc.contributor.authorCuestas, Daniel
dc.contributor.authorPerafan, Alejandra
dc.contributor.authorForero, Yency
dc.contributor.authorBonilla, Juan
dc.contributor.authorVelandia, Alexander
dc.contributor.authorGutierrez, Ana
dc.contributor.authorMotta Beltrán, Adriana
dc.contributor.authorHerrera, Hugo
dc.contributor.authorRolon, Mariam
dc.contributor.orcidMotta, Adriana [0000-0002-1924-1256]
dc.contributor.orcidMotta Beltrán, Adriana [0000-0002-1924-1256]
dc.contributor.orcidMotta Beltrán, Adriana [0000-0002-1924-1256]
dc.date.accessioned2020-03-25T14:24:28Z
dc.date.available2020-03-25T14:24:28Z
dc.description.abstractenglishIntroduction Angiokeratoma corporis diffusum are benign capillary malformations typically associated with Fabry disease and other lysosomal storage disorders. Only in a few cases they appear in healthy individuals. Methods and Case We carried out an exhaustive review of the literature on angiokeratomas and their main clinical, dermoscopy and histological features. Additionally, we reviewed the cases of healthy subjects illustrating the limitations of each case and comparing these results with our case. Discussion Angiokeratoma corporis diffusum is mostly related to Fabry disease and other lysosomal storage disorders. However, some cases may occur in apparently healthy individuals. Therefore, there is a increasing interest in its etiology, pathogenesis and clinical evaluation. Conclusion This is an academic–clinical review on angiokeratomas and their main implications in daily dermatological practice. Additionally, we report the first case in the literature of angiokeratoma corporis diffusum in a healthy patient with up‐to‐date laboratory methods currently available. The clinician should remember that not all angiokeratoma corporis diffusum occurs with lysosomal storage disorders.eng
dc.format.mimetypeapplication/pdf
dc.identifier.doihttps://doi.org/10.1111/ijd.14330
dc.identifier.instnameinstname:Universidad El Bosquespa
dc.identifier.issn0011-9059
dc.identifier.reponamereponame:Repositorio Institucional Universidad El Bosquespa
dc.identifier.repourlrepourl:https://repositorio.unbosque.edu.co
dc.identifier.urihttps://hdl.handle.net/20.500.12495/2111
dc.language.isoeng
dc.publisherWileyspa
dc.publisher.journalInternational Journal of Dermatologyspa
dc.relation.ispartofseriesInternational Journal of Dermatology, 0011-9059, Vol 58, Num 6, pag 713-721spa
dc.relation.urihttps://onlinelibrary.wiley.com/doi/abs/10.1111/ijd.14330
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.rights.accessrightshttps://purl.org/coar/access_right/c_abf113
dc.rights.creativecommons2019
dc.rights.localAcceso cerradospa
dc.subject.decsEnfermedad de Fabryspa
dc.subject.decsEnfermedades por almacenamiento lisosomal del sistema nerviosospa
dc.subject.decsNeoplasias de tejido vascularspa
dc.titleAngiokeratomas, not everything is fabry diseasespa
dc.title.translatedAngiokeratomas, not everything is fabry disease
dc.typearticlespa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersion
dc.type.localartículospa

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