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dc.contributores-ES
dc.creatorFich S, Félix; 1Departmento de Dermatología, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
dc.creatorChahuán Y, Marco; Departamento de Medicina, Campus Centro, Facultad de Medicina, Universidad de Chile y Servicio de Medicina, Hospital San Borja-Arriarán. Santiago, Chile.
dc.creatorFarías N, M. Magdalena; Departamento de Nutrición, Diabetes y Metabolismo, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile
dc.creatorCárdenas D, Consuelo; Departmento de Dermatología, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
dc.creatorAbarzúa A, Álvaro; Departmento de Dermatología, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
dc.creatorAraya C, Gabriela; Departmento de Dermatología, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
dc.creatorGonzález B, Sergio; Departamento de Anatomía Patológica, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
dc.date2012-03-23
dc.date.accessioned2019-11-11T18:27:37Z
dc.date.available2019-11-11T18:27:37Z
dc.identifierhttp://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/view/1507
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/111218
dc.descriptionAA AMYLOIDOSIS WITH CUTANEOUS MANIFESTATIONS. REPORT OF ONE CASE Systemic amyloidosis is a rare disease that can affect any organ. Its clinical manifestations are varied and nonspecific. The skin involvement of this disease is common and can be easily recognized on physical examination.  We report a 57 years old male presenting with a two years history of malaise, dyspnea and myalgias. On physical examination, ungueal dystrophy, orange pigmentation of eyelids with periocular petechiae and mild macroglossia were observed. Incisional biopsies of the eyelids, cheeks and hands were obtained. The pathological study demonstrated amyloid deposits. Since protein electrophoresis was normal, the diagnosis of AA amyloidosis was postulated.es-ES
dc.languagees
dc.publisherRevista Médica de Chilees-ES
dc.relationhttp://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1507/2619
dc.relationhttp://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1507/2620
dc.relationhttp://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1507/4598
dc.relationhttp://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1507/4599
dc.relationhttp://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1507/4937
dc.relationhttp://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1507/4938
dc.relationhttp://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1507/4939
dc.relationhttp://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1507/4940
dc.relationhttp://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1507/4941
dc.sourceRevista Médica de Chile; Vol. 140, núm. 4 (2012): ABRIL 2012es-ES
dc.source0034-9887
dc.subjectAmyloid; Amyloidosis; Skin diseaseses-ES
dc.titleManifestaciones cutáneas de amiloidosis sistémica como clave diagnóstica: A propósito de un caso.es-ES
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typees-ES


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