Colagenosis perforante reactiva adquirida: Caso clínico

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dc.catalogadorpau
dc.contributor.authorCárdenas D., Consuelo
dc.contributor.authorBello C., Cristina
dc.contributor.authorUribe G., Pablo
dc.contributor.authorRomero G., William
dc.contributor.authorGonzález Bombardiere, Sergio
dc.date.accessioned2023-05-18T19:49:41Z
dc.date.available2023-05-18T19:49:41Z
dc.date.issued2010
dc.description.abstractAcquired reactive perforating collagenosis is a perforating dermatosis characterized by transepidermal elimination of collagen. It is frequently associated to diabetes mellitus and chronic renal insufficiency, but it is also related to other systemic diseases. The lesions tend to resolve once the underlying condition is treated. We report two patients with the condition. A 65 year-old diabetic female on hemodialysis consulted for multiple itching cutaneous ulcers lasting one year. On physical examination, hyperpigmented papules and nodules were observed. A 65 year-old female with chronic renal failure in hemodialysis consulted for itching lesions in hands, forearms and arms. On physical examination, hyperpigmented lesions with ulcers, erosions and crusts were observed. In both cases, the pathological study of the lesions disclosed a reactive perforating collagenosis.
dc.format.extent4 páginas
dc.fuente.origenORCID
dc.identifier.doi10.4067/s0034-98872010001100012
dc.identifier.issn0034-9887
dc.identifier.urihttp://dx.doi.org/10.4067/S0034-98872010001100012
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/67085
dc.information.autorucEscuela de Medicina ; González Bombardiere, Sergio ; S/I ; 99856
dc.issue.numero10
dc.language.isoes
dc.nota.accesoContenido completo
dc.pagina.final1284
dc.pagina.inicio1281
dc.revistaRevista Médica de Chile
dc.rightsacceso abierto
dc.subjectCollagen diseases
dc.subjectDiabetes mellitus
dc.subjectSkin diseases, vesiculobullous
dc.subject.ddc610
dc.subject.deweyMedicina y saludes_ES
dc.titleColagenosis perforante reactiva adquirida: Caso clínico
dc.title.alternativeAcquired reactive perforating collagenosis. Report of two cases
dc.typeartículo
dc.volumen138
sipa.codpersvinculados99856
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