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        "resumen" => "<span class="elsevierStyleSectionTitle">Background</span><p class="elsevierStyleSimplePara elsevierViewall">Sebaceous gland tumors are a rare type of neoplasm&#46; In some cases they have been associated with visceral tumors in patients with Muir-Torre syndrome&#44; a hereditary form of nonpolyposis colorectal cancer&#46; The aim of this study was to review the diagnosis and follow-up of a series of patients with sebaceous gland tumors to assess how many met the criteria for Muir-Torre syndrome&#46;</p> <span class="elsevierStyleSectionTitle">Patients and methods</span><p class="elsevierStyleSimplePara elsevierViewall">A search was performed of records from 1990 to 2005 in the database of the Department of Dermatology of the Consorcio Hospital General Universitario de Valencia in Valencia&#44; Spain&#44; to identify patients with sebaceous gland tumors&#46; The biopsy material was reviewed to confirm the diagnosis&#46; We also searched the patient histories for information suggestive of a diagnosis of Muir-Torre syndrome&#59; when the histories were incomplete&#44; we contacted the patients by telephone&#46;</p> <span class="elsevierStyleSectionTitle">Results</span><p class="elsevierStyleSimplePara elsevierViewall">We identified 20 patients diagnosed with sebaceous gland tumors&#44; but after reviewing the biopsy material diagnosis was only confirmed in 12&#46; Two patients belonged to a family with a history of visceral tumors that met the clinical criteria for hereditary nonpolyposis colorectal cancer syndrome&#46; Follow-up was not uniform in all patients and not all underwent the same tests&#46;</p> <span class="elsevierStyleSectionTitle">Conclusions</span><p class="elsevierStyleSimplePara elsevierViewall">It is essential to rule out the presence of Muir-Torre syndrome in patients with sebaceous gland tumors&#46; The use of new techniques such as immunohistochemistry or detection of microsatellite instability may help to identify families at increased risk of Muir-Torre syndrome&#46;</p>"
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        "resumen" => "<span class="elsevierStyleSectionTitle">Introducci&#243;n</span><p class="elsevierStyleSimplePara elsevierViewall">Los tumores seb&#225;ceos son un grupo infrecuente de neoplasias&#46; En algunos casos se han relacionado con neoplasias viscerales en pacientes con el s&#237;ndrome de Muir-Torre&#59; una variante cl&#237;nica del s&#237;ndrome de c&#225;ncer de colon hereditario no polip&#243;sico&#46; El objetivo de este trabajo es revisar el diagn&#243;stico y el seguimiento de una serie de pacientes con tumores seb&#225;ceos para comprobar cu&#225;ntos de ellos cumpl&#237;an criterios de s&#237;ndrome de Muir-Torre&#46;</p> <span class="elsevierStyleSectionTitle">Pacientes y m&#233;todos</span><p class="elsevierStyleSimplePara elsevierViewall">Se realiz&#243; una b&#250;squeda en la base de datos del Servicio de Dermatolog&#237;a del Consorcio Hospital General Universitario de Valencia entre 1990 y 2005&#44; buscando pacientes con tumores seb&#225;ceos&#46; Se revisaron las biopsias para confirmar el diagn&#243;stico&#46; Tambi&#233;n buscamos datos en las historias cl&#237;nicas que sugiriesen un diagn&#243;stico de s&#237;ndrome de Muir-Torre&#44; cuando las historias estaban incompletas nos pusimos en contacto por tel&#233;fono con los pacientes&#46;</p> <span class="elsevierStyleSectionTitle">Resultados</span><p class="elsevierStyleSimplePara elsevierViewall">Encontramos 20 pacientes diagnosticados de tumores seb&#225;ceos&#44; pero despu&#233;s de revisar la biopsia s&#243;lo confirmamos este diagn&#243;stico en 12 pacientes&#46; Dos pacientes pertenec&#237;an a una familia con antecedentes de neoplasias viscerales&#44; que cumpl&#237;a los criterios cl&#237;nicos de s&#237;ndrome de c&#225;ncer de colon hereditario no polip&#243;sico&#46; No hubo un seguimiento uniforme de los pacientes ni se realizaron las mismas pruebas en todos ellos&#46;</p> <span class="elsevierStyleSectionTitle">Conclusiones</span><p class="elsevierStyleSimplePara elsevierViewall">Es fundamental descartar la presencia de un s&#237;ndrome de Muir-Torre en pacientes con tumores seb&#225;ceos&#46; El uso de nuevas t&#233;cnicas como la detecci&#243;n de la inestabilidad de microsat&#233;lites o la inmunohistoqu&#237;mica pueden ayudar a detectar a las familias que tienen un mayor riesgo de padecer el s&#237;ndrome de Muir-Torre&#46;</p>"
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Original articles
Clinical Follow-up and Presence of Visceral Tumors in 12 Patients With Sebaceous Gland Tumors
Tumores Sebáceos: Seguimiento Clínico y Presencia de Neoplasias en Una Serie de 12 Pacientes
P. Mercadera,
Autor para correspondencia
pedromercader@hotmail.com

Correspondence: Servicio de Dermatología, Hospital Morales Meseguer, Avda/Marqués de los Vélez, s/n., 30008 Murcia, Spain.
, M.L. García-Melgaresb, E. Rocheb, J.L. Sánchez-Carazob, V. Alegre-de Miquelb
a Servicio de Dermatología, Hospital General Universitario Morales Meseguer, Murcia, Spain
b Servicio de Dermatología, Consorcio Hospital General Universitario de Valencia, Valencia, Spain
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        "resumen" => "<span class="elsevierStyleSectionTitle">Background</span><p class="elsevierStyleSimplePara elsevierViewall">Sebaceous gland tumors are a rare type of neoplasm&#46; In some cases they have been associated with visceral tumors in patients with Muir-Torre syndrome&#44; a hereditary form of nonpolyposis colorectal cancer&#46; The aim of this study was to review the diagnosis and follow-up of a series of patients with sebaceous gland tumors to assess how many met the criteria for Muir-Torre syndrome&#46;</p> <span class="elsevierStyleSectionTitle">Patients and methods</span><p class="elsevierStyleSimplePara elsevierViewall">A search was performed of records from 1990 to 2005 in the database of the Department of Dermatology of the Consorcio Hospital General Universitario de Valencia in Valencia&#44; Spain&#44; to identify patients with sebaceous gland tumors&#46; The biopsy material was reviewed to confirm the diagnosis&#46; We also searched the patient histories for information suggestive of a diagnosis of Muir-Torre syndrome&#59; when the histories were incomplete&#44; we contacted the patients by telephone&#46;</p> <span class="elsevierStyleSectionTitle">Results</span><p class="elsevierStyleSimplePara elsevierViewall">We identified 20 patients diagnosed with sebaceous gland tumors&#44; but after reviewing the biopsy material diagnosis was only confirmed in 12&#46; Two patients belonged to a family with a history of visceral tumors that met the clinical criteria for hereditary nonpolyposis colorectal cancer syndrome&#46; Follow-up was not uniform in all patients and not all underwent the same tests&#46;</p> <span class="elsevierStyleSectionTitle">Conclusions</span><p class="elsevierStyleSimplePara elsevierViewall">It is essential to rule out the presence of Muir-Torre syndrome in patients with sebaceous gland tumors&#46; The use of new techniques such as immunohistochemistry or detection of microsatellite instability may help to identify families at increased risk of Muir-Torre syndrome&#46;</p>"
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Información del artículo
ISSN: 15782190
Idioma original: Inglés
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