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        "resumen" => "<span class="elsevierStyleSectionTitle">Objetivo</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">An&#225;lisis descriptivo de los datos cl&#237;nicos&#44; exploraciones complementarias y r&#233;gimen terap&#233;utico de los pacientes diagnosticados de dermatomiositis juvenil en nuestro centro&#44; un hospital terciario&#46;</p> <span class="elsevierStyleSectionTitle">M&#233;todos</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Estudio retrospectivo de las historias cl&#237;nicas de los ni&#241;os con diagn&#243;stico definitivo de dermatomiositis juvenil seguidos en la consulta de reumatolog&#237;a pedi&#225;trica de nuestro centro&#44; desde 1986 hasta julio de 1999&#46;</p> <span class="elsevierStyleSectionTitle">Resultados</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Del total de 9 casos recogidos&#44; 3 han sido varones y 6 mujeres&#46; La edad media al diagn&#243;stico fue de 7 a&#241;os&#46; Los s&#237;ntomas y signos que demandaron atenci&#243;n hospitalaria fueron&#58; debilidad y dolor muscular asociados a s&#237;ndrome constitucional en 4 casos &#40;44&#37;&#41;&#59; debilidad muscular aislada en 2 casos&#59; dolor muscular y s&#237;ndrome constitucional en un caso&#44; y monoartritis en otro&#46; Un paciente present&#243; cl&#237;nica exclusivamente cut&#225;nea al inicio&#46; Presentaron calcinosis 3 pacientes&#46; En 8 casos se produjo una elevaci&#243;n de la creatinfosfocinasa s&#233;rica y la lactatodeshidrogenasa en 8 pacientes&#59; en 7 casos&#44; una elevaci&#243;n de la aldolasa&#44; y en 6 casos&#44; en 8 pacientes un aumento de las aminotransferasas&#46; Los autoanticuerpos fueron negativos en todos los pacientes&#46; El electromiograma objetiv&#243; un patr&#243;n miop&#225;tico o mixto en los 5 casos en que se realiz&#243;&#46; La biopsia muscular fue diagn&#243;stica en todos los casos&#46; Siete pacientes recibieron tratamiento con corticoides y 2 pacientes corticoides&#44; metotrexato y gammaglobulina&#46; En cuanto a la evoluci&#243;n&#44; 6 pacientes se encuentran asintom&#225;ticos&#44; en 2 persiste debilidad muscular leve aislada y un paciente ha fallecido&#46;</p> <span class="elsevierStyleSectionTitle">Conclusiones</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Los resultados en nuestra serie concuerdan con la bibliograf&#237;a&#46; La dermatomiositis juvenil debe ser sospechada en ni&#241;os con debilidad muscular y afectaci&#243;n del estado general&#46; Se recomienda comenzar precozmente el tratamiento con corticoides&#46;</p>"
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        "resumen" => "<span class="elsevierStyleSectionTitle">Objective</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">The aim of this study is to review the presenting signs and symptoms&#44; laboratory findings and therapeutic regimens of juvenile dermatomyositis in a tertiary hospital&#46;</p> <span class="elsevierStyleSectionTitle">Methods</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">We reviewed retrospectively the available medical records of patients who met the clinicopathologic criteria of Bohan and Peter for definite juvenile dermatomyositis&#46; They were followed between 1986 and july 1999 at the pediatric rheumatology section at our institution&#46;</p> <span class="elsevierStyleSectionTitle">Results</span><p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">The patient population included 3 male and 6 female patients&#46; The mean age at diagnosis was 7 years&#46; Clinical features demanding medical attention at the hospital were&#58; muscle weakness and pain&#44; with associated general symptoms in 4 cases&#59; isolated muscle weakness in 2 cases&#59; muscle weakness associated to general symptoms in 1 case&#59; and monoarthritis in another case&#46; One patient presented initially only with cutaneous rash&#46; Three patients developed calcinosis&#46; Serum CPK and LDH levels were elevated in 8 patients&#44; aldolase in 7 and aminotransferases in 6&#46; Autoantibodies were undetectable in all the patients&#46; Electomyography demonstrated myopatic or mixed pattern in the 5 patients it was practiced&#46; Muscle biopsy showed features of inflammatory myopathy in all the cases&#46; Seven patients were treated exclusively with steroids and 2 patients with steroids&#44; methotrexate and intravenous gammaglobuline&#46; Actually&#44; 6 patients are asymptomatic&#44; 2 have mild muscle weakness&#44; and 1 has died&#46;</p> <span class="elsevierStyleSectionTitle">Conclusions</span><p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">The results of our review agree with other series reported&#46; Juvenile dermatomyositis suspicious should be made upon muscle weakness and general symptoms&#46;</p><p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Treatment with steroids should be started promptly&#46;</p>"
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Dermatomiositis en la infancia
Dermatomyositis in childhood
M.E. Mateos Gonzáleza,*, E. López-Lasoa, J. Gómez Reinob, R. Simón de las Herasa, F. Mateos Beatoa
a Unidad de Neurología Pediátrica.
b Unidad de Reumatología Pediátrica. Departamento de Pediatría. Hospital 12 de Octubre. Madrid.
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      "en" => array:1 [
        "titulo" => "Dermatomyositis in childhood"
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    "fechaRecibido" => "1999-09-30"
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            0 => "Dermatomiositis juvenil"
            1 => "Ni&#241;os"
            2 => "Dermatomiositis-tratamiento"
            3 => "Miopat&#237;as inflamatorias"
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          "clase" => "keyword"
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            0 => "Juvenile Dermatomyositis"
            1 => "Children"
            2 => "Dermatomyositisdrug therapy"
            3 => "Inflammatory myopathies"
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        "resumen" => "<span class="elsevierStyleSectionTitle">Objetivo</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">An&#225;lisis descriptivo de los datos cl&#237;nicos&#44; exploraciones complementarias y r&#233;gimen terap&#233;utico de los pacientes diagnosticados de dermatomiositis juvenil en nuestro centro&#44; un hospital terciario&#46;</p> <span class="elsevierStyleSectionTitle">M&#233;todos</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Estudio retrospectivo de las historias cl&#237;nicas de los ni&#241;os con diagn&#243;stico definitivo de dermatomiositis juvenil seguidos en la consulta de reumatolog&#237;a pedi&#225;trica de nuestro centro&#44; desde 1986 hasta julio de 1999&#46;</p> <span class="elsevierStyleSectionTitle">Resultados</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Del total de 9 casos recogidos&#44; 3 han sido varones y 6 mujeres&#46; La edad media al diagn&#243;stico fue de 7 a&#241;os&#46; Los s&#237;ntomas y signos que demandaron atenci&#243;n hospitalaria fueron&#58; debilidad y dolor muscular asociados a s&#237;ndrome constitucional en 4 casos &#40;44&#37;&#41;&#59; debilidad muscular aislada en 2 casos&#59; dolor muscular y s&#237;ndrome constitucional en un caso&#44; y monoartritis en otro&#46; Un paciente present&#243; cl&#237;nica exclusivamente cut&#225;nea al inicio&#46; Presentaron calcinosis 3 pacientes&#46; En 8 casos se produjo una elevaci&#243;n de la creatinfosfocinasa s&#233;rica y la lactatodeshidrogenasa en 8 pacientes&#59; en 7 casos&#44; una elevaci&#243;n de la aldolasa&#44; y en 6 casos&#44; en 8 pacientes un aumento de las aminotransferasas&#46; Los autoanticuerpos fueron negativos en todos los pacientes&#46; El electromiograma objetiv&#243; un patr&#243;n miop&#225;tico o mixto en los 5 casos en que se realiz&#243;&#46; La biopsia muscular fue diagn&#243;stica en todos los casos&#46; Siete pacientes recibieron tratamiento con corticoides y 2 pacientes corticoides&#44; metotrexato y gammaglobulina&#46; En cuanto a la evoluci&#243;n&#44; 6 pacientes se encuentran asintom&#225;ticos&#44; en 2 persiste debilidad muscular leve aislada y un paciente ha fallecido&#46;</p> <span class="elsevierStyleSectionTitle">Conclusiones</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Los resultados en nuestra serie concuerdan con la bibliograf&#237;a&#46; La dermatomiositis juvenil debe ser sospechada en ni&#241;os con debilidad muscular y afectaci&#243;n del estado general&#46; Se recomienda comenzar precozmente el tratamiento con corticoides&#46;</p>"
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        "resumen" => "<span class="elsevierStyleSectionTitle">Objective</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">The aim of this study is to review the presenting signs and symptoms&#44; laboratory findings and therapeutic regimens of juvenile dermatomyositis in a tertiary hospital&#46;</p> <span class="elsevierStyleSectionTitle">Methods</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">We reviewed retrospectively the available medical records of patients who met the clinicopathologic criteria of Bohan and Peter for definite juvenile dermatomyositis&#46; They were followed between 1986 and july 1999 at the pediatric rheumatology section at our institution&#46;</p> <span class="elsevierStyleSectionTitle">Results</span><p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">The patient population included 3 male and 6 female patients&#46; The mean age at diagnosis was 7 years&#46; Clinical features demanding medical attention at the hospital were&#58; muscle weakness and pain&#44; with associated general symptoms in 4 cases&#59; isolated muscle weakness in 2 cases&#59; muscle weakness associated to general symptoms in 1 case&#59; and monoarthritis in another case&#46; One patient presented initially only with cutaneous rash&#46; Three patients developed calcinosis&#46; Serum CPK and LDH levels were elevated in 8 patients&#44; aldolase in 7 and aminotransferases in 6&#46; Autoantibodies were undetectable in all the patients&#46; Electomyography demonstrated myopatic or mixed pattern in the 5 patients it was practiced&#46; Muscle biopsy showed features of inflammatory myopathy in all the cases&#46; Seven patients were treated exclusively with steroids and 2 patients with steroids&#44; methotrexate and intravenous gammaglobuline&#46; Actually&#44; 6 patients are asymptomatic&#44; 2 have mild muscle weakness&#44; and 1 has died&#46;</p> <span class="elsevierStyleSectionTitle">Conclusions</span><p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">The results of our review agree with other series reported&#46; Juvenile dermatomyositis suspicious should be made upon muscle weakness and general symptoms&#46;</p><p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Treatment with steroids should be started promptly&#46;</p>"
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ISSN: 16954033
Idioma original: Español
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