Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/329966
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dc.contributor.CRUESPUNIVERSIDADE DE ESTADUAL DE CAMPINASpt_BR
dc.contributor.authoremailanacarolina.bsala@gmail.compt_BR
dc.typeArtigopt_BR
dc.titleScleromyxedema: Clinical Diagnosis And Autopsy Findingsen
dc.contributor.authorBulhoes Salapt_BR
dc.contributor.authorAna Carolina; Cunhapt_BR
dc.contributor.authorPaulo Rowilson; Lopes Pintopt_BR
dc.contributor.authorClovis Antonio; Xavier de Moraes Alvespt_BR
dc.contributor.authorCelia Antonia; Paivapt_BR
dc.contributor.authorIngrid Barreto; Vieira Araujopt_BR
dc.contributor.authorAna Paulapt_BR
unicamp.author[Bulhoes Sala, Ana Carolina] Univ Estadual Campinas UNICAMP, Campinas, SP, Brazilpt_BR
unicamp.author.external[Bulhoes Sala, Ana Carolinapt_BR
unicamp.author.externalCunha, Paulo Rowilsonpt_BR
unicamp.author.externalLopes Pinto, Clovis Antoniopt_BR
unicamp.author.externalXavier de Moraes Alves, Celia Antoniapt_BR
unicamp.author.externalPaiva, Ingrid Barretopt_BR
unicamp.author.externalVieira Araujo, Ana Paula] FMI, Jundiai, SP, Brazilpt_BR
unicamp.author.external[Paiva, Ingrid Barreto] Private Clin, Vitoria, ES, Brazilpt_BR
unicamp.author.external[Vieira Araujo, Ana Paula] Private Clin, Sao Luis, MA, Brazilpt_BR
dc.subjectAutopsyen
dc.subjectCyclophosphamideen
dc.subjectParaproteinemiasen
dc.subjectScleromyxedemaen
dc.description.abstractScleromyxedema is a rare chronic cutaneous mucinosis of unknown etiology. It is characterized by papular eruption and scleroderma with microscopic evidence of mucin deposition, fibroblast proliferation, and fibrosis. Most patients with scleromyxedema have monoclonal gammopathy and systemic manifestations resulting in significant morbidity and mortality. Several types of treatment have been reported with partial or inconsistent responses. Despite showing unpredictable evolution, systemic consequences of scleromyxedema and treatment side effects may result in death. We describe a rare case of a patient with scleromyxedema without paraproteinemia with systemic involvement that evolved to death despite treatment with cyclophosphamide.en
dc.relation.ispartofAnais Brasileiros de Dermatologiapt_BR
dc.publisherSoc Brasileira Dermatologiapt_BR
dc.publisherRio de Janeiropt_BR
dc.date.issued2016pt_BR
dc.date.monthofcirculationset-outpt_BR
dc.identifier.citationAnais Brasileiros De Dermatologia. Soc Brasileira Dermatologia, v. 91, p. 48 - 50, 2016.pt_BR
dc.language.isoEnglishpt_BR
dc.description.volume91pt_BR
dc.description.issuenumber5pt_BR
dc.description.issuesupplement1pt_BR
dc.description.firstpage48pt_BR
dc.description.lastpage50pt_BR
dc.rightsabertopt_BR
dc.sourceWOSpt_BR
dc.identifier.issn0365-0596pt_BR
dc.identifier.eissn1806-4841pt_BR
dc.identifier.wosidWOS:000396341200013pt_BR
dc.identifier.doi10.1590/abd1806-4841.20164527pt_BR
dc.identifier.urlhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962016001100048&lng=en&tlng=enpt_BR
dc.date.available2017-11-13T13:56:56Z-
dc.date.accessioned2017-11-13T13:56:56Z-
dc.description.provenanceMade available in DSpace on 2017-11-13T13:56:56Z (GMT). No. of bitstreams: 1 000396341200013.pdf: 290006 bytes, checksum: 491b3d713a18b3dad2cee0c4ce0e192d (MD5) Previous issue date: 2016en
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/329966-
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