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        "titulo" => "Abstract"
        "resumen" => "<span class="elsevierStyleSectionTitle">Introduction</span><p class="elsevierStyleSimplePara elsevierViewall">Porokeratosis is a rare disorder of keratinization&#46; The presence of amyloid deposits has been observed in inflammatory and tumoral skin diseases&#46;</p> <span class="elsevierStyleSectionTitle">Objectives</span><p class="elsevierStyleSimplePara elsevierViewall">The aim of this study was to determine the frequency of cutaneous amyloidosis in histology samples from various types of porokeratosis diagnosed in our department from 1988 to 2005&#46;</p> <span class="elsevierStyleSectionTitle">Material and methods</span><p class="elsevierStyleSimplePara elsevierViewall">Thirty patients were selected and 34 biopsies of lesions clinically and histologically compatible with porokeratosis were performed&#46; Sections were stained with hematoxylin-eosin and thioflavin T&#46;</p> <span class="elsevierStyleSectionTitle">Results</span><p class="elsevierStyleSimplePara elsevierViewall">Amyloid deposits were observed in 11 biopsies from 9 patients&#46; Most were women in their sixties&#44; with disseminated superficial actinic porokeratosis that had begun at least 5 years earlier&#46; No notable histologic differences were observed between porokeratosis specimens with and without amyloid deposits&#46;</p> <span class="elsevierStyleSectionTitle">Conclusions</span><p class="elsevierStyleSimplePara elsevierViewall">The coexistence of porokeratosis and amyloidosis is a rare occurrence but may be underdiagnosed&#46; In our opinion&#44; the advanced age of the patients and the chronic nature of the lesions would have been predisposing factors for amyloid deposition&#46; The possibility of racial or genetic influences&#44; however&#44; cannot be ruled out&#46;</p>"
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        "resumen" => "<span class="elsevierStyleSectionTitle">Introducci&#243;n</span><p class="elsevierStyleSimplePara elsevierViewall">Las poroqueratosis son alteraciones de la queratinizaci&#243;n poco frecuentes&#46; La presencia de material amiloide se ha observado en dermatosis de etiolog&#237;a inflamatoria y tumoral&#46;</p> <span class="elsevierStyleSectionTitle">Objetivos</span><p class="elsevierStyleSimplePara elsevierViewall">Determinar la incidencia de amiloidosis cut&#225;nea en las muestras histol&#243;gicas de distintos tipos de poroqueratosis diagnosticados en nuestro servicio entre 1988-2005&#46;</p> <span class="elsevierStyleSectionTitle">Material y m&#233;todos</span><p class="elsevierStyleSimplePara elsevierViewall">Se seleccionaron 30 pacientes y se realizaron 34 biopsias de lesiones compatibles cl&#237;nica e histol&#243;gicamente con poroqueratosis&#46; Se realizaron tinciones con hematoxilina-eosina y tioflavina T en todas ellas&#46;</p> <span class="elsevierStyleSectionTitle">Resultados</span><p class="elsevierStyleSimplePara elsevierViewall">Se detectaron dep&#243;sitos de amiloide en 11 biopsias que pertenec&#237;an a 9 pacientes&#46; La mayor&#237;a eran mujeres en la sexta d&#233;cada de la vida&#44; con la variante de poroqueratosis act&#237;nica superficial diseminada y con un tiempo de evoluci&#243;n superior a 5 a&#241;os&#46; No se encontraron diferencias histol&#243;gicas significativas entre las biopsias de poroqueratosis con amiloide y sin &#233;l&#44; a excepci&#243;n del material an&#243;malo&#46;</p> <span class="elsevierStyleSectionTitle">Conclusiones</span><p class="elsevierStyleSimplePara elsevierViewall">La coexistencia de poroqueratosis y amiloidosis es un hecho poco frecuente&#44; posiblemente infradiagnosticado&#46; Consideramos que la edad avanzada y la cronicidad de las lesiones ser&#237;an factores predisponentes&#44; sin poder descartarse una implicaci&#243;n racial o gen&#233;tica&#46;</p>"
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Original article
Localized Cutaneous Amyloidosis Secondary to Porokeratosis: A Retrospective Histopathologic Study of 30 Patients
Amiloidosis Cutánea Localizada Secundaria A Poroqueratosis. Estudio Histopatológico Retrospectivo de 30 Pacientes
A. Ramírez-Santos
Corresponding author
jaime.toribio@usc.es

Correspondence: Departamento de Dermatología, Facultad de Medicina, C/ San Francisco, s/n 15782 Santiago de Compostela, La Coruña, Spain.
, O. Suárez-Amor, L. Pérez-Pérez, M. Loureiro, C. Peteiro, J. Toribio
Servicio de Dermatología, Facultad de Medicina, Santiago de Compostela, La Coruña, Spain
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        "resumen" => "<span class="elsevierStyleSectionTitle">Introduction</span><p class="elsevierStyleSimplePara elsevierViewall">Porokeratosis is a rare disorder of keratinization&#46; The presence of amyloid deposits has been observed in inflammatory and tumoral skin diseases&#46;</p> <span class="elsevierStyleSectionTitle">Objectives</span><p class="elsevierStyleSimplePara elsevierViewall">The aim of this study was to determine the frequency of cutaneous amyloidosis in histology samples from various types of porokeratosis diagnosed in our department from 1988 to 2005&#46;</p> <span class="elsevierStyleSectionTitle">Material and methods</span><p class="elsevierStyleSimplePara elsevierViewall">Thirty patients were selected and 34 biopsies of lesions clinically and histologically compatible with porokeratosis were performed&#46; Sections were stained with hematoxylin-eosin and thioflavin T&#46;</p> <span class="elsevierStyleSectionTitle">Results</span><p class="elsevierStyleSimplePara elsevierViewall">Amyloid deposits were observed in 11 biopsies from 9 patients&#46; Most were women in their sixties&#44; with disseminated superficial actinic porokeratosis that had begun at least 5 years earlier&#46; No notable histologic differences were observed between porokeratosis specimens with and without amyloid deposits&#46;</p> <span class="elsevierStyleSectionTitle">Conclusions</span><p class="elsevierStyleSimplePara elsevierViewall">The coexistence of porokeratosis and amyloidosis is a rare occurrence but may be underdiagnosed&#46; In our opinion&#44; the advanced age of the patients and the chronic nature of the lesions would have been predisposing factors for amyloid deposition&#46; The possibility of racial or genetic influences&#44; however&#44; cannot be ruled out&#46;</p>"
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        "resumen" => "<span class="elsevierStyleSectionTitle">Introducci&#243;n</span><p class="elsevierStyleSimplePara elsevierViewall">Las poroqueratosis son alteraciones de la queratinizaci&#243;n poco frecuentes&#46; La presencia de material amiloide se ha observado en dermatosis de etiolog&#237;a inflamatoria y tumoral&#46;</p> <span class="elsevierStyleSectionTitle">Objetivos</span><p class="elsevierStyleSimplePara elsevierViewall">Determinar la incidencia de amiloidosis cut&#225;nea en las muestras histol&#243;gicas de distintos tipos de poroqueratosis diagnosticados en nuestro servicio entre 1988-2005&#46;</p> <span class="elsevierStyleSectionTitle">Material y m&#233;todos</span><p class="elsevierStyleSimplePara elsevierViewall">Se seleccionaron 30 pacientes y se realizaron 34 biopsias de lesiones compatibles cl&#237;nica e histol&#243;gicamente con poroqueratosis&#46; Se realizaron tinciones con hematoxilina-eosina y tioflavina T en todas ellas&#46;</p> <span class="elsevierStyleSectionTitle">Resultados</span><p class="elsevierStyleSimplePara elsevierViewall">Se detectaron dep&#243;sitos de amiloide en 11 biopsias que pertenec&#237;an a 9 pacientes&#46; La mayor&#237;a eran mujeres en la sexta d&#233;cada de la vida&#44; con la variante de poroqueratosis act&#237;nica superficial diseminada y con un tiempo de evoluci&#243;n superior a 5 a&#241;os&#46; No se encontraron diferencias histol&#243;gicas significativas entre las biopsias de poroqueratosis con amiloide y sin &#233;l&#44; a excepci&#243;n del material an&#243;malo&#46;</p> <span class="elsevierStyleSectionTitle">Conclusiones</span><p class="elsevierStyleSimplePara elsevierViewall">La coexistencia de poroqueratosis y amiloidosis es un hecho poco frecuente&#44; posiblemente infradiagnosticado&#46; Consideramos que la edad avanzada y la cronicidad de las lesiones ser&#237;an factores predisponentes&#44; sin poder descartarse una implicaci&#243;n racial o gen&#233;tica&#46;</p>"
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Article information
ISSN: 15782190
Original language: English
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Idiomas
Actas Dermo-Sifiliográficas
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