Enfermedad de Cowden: presentación de un caso y revisión de la bibliografía*
Cowden disease: report of a case and review of the bibliography
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Tomás Escalonilla, 5-5.<span class="elsevierStyleSup">o</span>C. 29010 Málaga." ] ] ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Cowden disease: report of a case and review of the bibliography" ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2000-10-31" "fechaAceptado" => "2001-01-11" "PalabrasClave" => array:2 [ "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec226956" "palabras" => array:3 [ 0 => "Enfermedad de Cowden" 1 => "Poliposis gastrointestinal" 2 => "Hamartomas" ] ] ] "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Key words" "identificador" => "xpalclavsec226955" "palabras" => array:3 [ 0 => "Cowden disease" 1 => "Gastrointestinal polyposis" 2 => "Hamartomas" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">La Enfermedad de Cowden (EC), también conocida como «Síndrome de Neoplasias-Hamartomas Múltiples», es una rara e infra-diagnosticada entidad hereditaria autosómica dominante caracterizada por la presencia de múltiples hamartomas de origen mesodérmico, en-dodérmico y ectodérmico, así como por una alta incidencia de presen-tación de tumores malignos. Actualmente se clasifica como un síndro-me preneoplásico hereditario.</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Describimos los hallazgos en un paciente con EC con especial énfasis sobre los aspectos de imagen, revisando las principales manifesta-ciones de esta entidad.</p>" ] "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Cowden diasease (CD), also known as multiple hamartoma syndrome, is a rare and underdiagnosed autosomal dominant hereditary disorder characterized by the presence of multiple hamartomas originating in mesoderm, endoderm and ectoderm, and is associated with a hight incidence of malignant tumor development. It is presently considered a hereditary preneoplastic syndrome.</p><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">We report the our observations in a patient with CD, ocusing especially on the findings in imaging studies, and review the major features of this entity.</p>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "*" "nota" => "<p class="elsevierStyleNotepara">Vicente R, García-Gutiérrez Juan A, Mut J, et al. Enfermedad de Cowden: presentación de un caso y revisión de la bibliografía. Radiología 2001;43(1):38-41.</p>" ] ] "bibliografia" => array:2 [ "titulo" => "Bibliografía" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:17 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Cowden’s disease" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "K.M. 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| 2023 Noviembre | 6 | 24 | 30 |
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| 2023 Septiembre | 5 | 12 | 17 |
| 2023 Agosto | 0 | 7 | 7 |
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