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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">El Glioblastoma multiforme con agregaci&#243;n familiar es poco frecuente&#44; asoci&#225;ndose la mayor parte de los casos a s&#237;ndromes gen&#233;ticos conocidos &#40;como el s&#237;ndrome de Turcot&#44; el s&#237;ndrome de Li-Fraumeni&#44; la neurofibromatosis&#44; etc&#41;&#46; Sin embargo&#44; existen otros gliomas familiares no asociados a estos cuadros sindr&#243;micos que&#44; aunque menos frecuentes&#44; han mostrado unas caracter&#237;sticas etiol&#243;gicas y cl&#237;nicas diferentes a las de los gliomas espor&#225;dicos&#46;</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Por otra parte&#44; hasta un 10&#37; de los gliomas se consideran verdaderamente multic&#233;ntricos&#44; apareciendo de modo s&#237;ncrono o met&#225;crono&#46; Los glioblastomas de aparici&#243;n met&#225;crona han mostrado en algunos estudios un mejor pron&#243;stico&#44; habi&#233;ndose encontrado trastornos gen&#233;ticos diferentes en los tumores de un mismo paciente&#46;</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Los gliomas familiares con presentaci&#243;n met&#225;crona son excepcionales&#46; Estos tumores presentan unas implicaciones terap&#233;uticas especiales por la limitaci&#243;n del tratamiento radioter&#225;pico tras el tratamiento inicial&#46; Aunque se han identificado mutaciones variadas en estos pacientes&#44; la identificaci&#243;n precisa de dichos trastornos se basar&#225; en el estudio de su sustrato gen&#233;tico espec&#237;fico&#46; Presentamos un caso cl&#237;nico que combina ambas peculiaridades revisando las caracter&#237;sticas de esta patolog&#237;a&#46;</p>"
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        "titulo" => "Summary"
        "resumen" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Familial glioblastoma multiforme is a rather uncommon entity&#44; being in most cases associated to known genetic disorders &#40;as Turcot syndrome&#44; Li-Fraumeni syndrome&#44; neurofibromatosis&#44; etc&#46;&#41;&#46; However&#44; familial gliomas have also been described&#44; although less frequently&#44; independently of these genetic syndromes showing some special features regarding its etiology and clinical manifestations&#46;</p><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Less than 10&#37; of gliomas may be considered as true multicentric tumours either synchronous or metachronous in clinical presentation&#46; Metachronous glioblastomas have been associated to better prognosis in some studies&#44; with genetic studies having found clear differences among the tumors within same patients&#46;</p><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Familial glioblastoma with metachronous presentation is an exceptional disorder&#46; These tumors show special therapeutic implications due to the limitations of radiotherapy once the patient has already irradiated&#46; A variety of non-specific mutations have been found in these patients but true characterization of this disorder remains unclear and will be based on further genetic studies&#46; We present a clinical report on a patient harbouring a familial and metachronous glioblastoma&#46; The main aspects of this entity are reviwed&#46;</p>"
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Glioblastoma familiar múltiple de aparición metácrona: implicaciones etiopatogénicas y pronósticas
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Avila
Badajoz
Balears
Barcelona
Bizkaia
Burgos
Caceres
Cadiz
Cantabria
Castellon
Ceuta
Ciudad real
Cordoba
Cuenca
Girona
Granada
Guadalajara
Guipuzcoa
Huelva
Huesca
Jaen
La rioja
Las palmas
Leon
Lleida
Lugo
Madrid
Malaga
Melilla
Murcia
Navarra
Ourense
Palencia
Pontevedra
Salamanca
Segovia
Sevilla
Soria
Tarragona
Tenerife
Teruel
Toledo
Valencia
Valladolid
Zamora
Zaragoza
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Atención al cliente
Teléfono
Llamadas desde España
932 415 960
Llamadas desde el extranjero
+34 932 415 960
Horario de 9 a 18h. excepto los meses de julio y agosto que será de 9 a 15h.
Idiomas
Neurocirugía
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