Meningioangiomatosis. Descripción de dos casos y revisión de la literatura
Meningioangiomatosis: report of two cases and literature review
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"apellidos" => "Hinojosa" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "aff0010" ] ] ] ] "afiliaciones" => array:1 [ 0 => array:3 [ "entidad" => "Departamentos de Neurocirugía infantil. Hospital Universitario 12 de Octubre. Madrid" "etiqueta" => "<span class="elsevierStyleSup">*.</span>" "identificador" => "aff0010" ] ] ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Meningioangiomatosis: report of two cases and literature review" ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2005-02-01" "fechaAceptado" => "2005-02-18" "PalabrasClave" => array:2 [ "es" => array:2 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec159288" "palabras" => array:5 [ 0 => "Corteza cerebral" 1 => "Hamartoma, Leptomeninge" 2 => "Meningioangiomatosis" 3 => "Meningioma" 4 => "Tumor" ] ] 1 => array:4 [ "clase" => "abr" "titulo" => "Abreviaturas" "identificador" => "xpalclavsec159289" "palabras" => array:2 [ 0 => "MA" 1 => "NF" ] ] ] "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Key words" "identificador" => "xpalclavsec159290" "palabras" => array:6 [ 0 => "Cerebral cortex" 1 => "Hamartoma" 2 => "Leptomeninge" 3 => "Meningioangiomatosis" 4 => "Meningioma" 5 => "Tumour" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">La Meningioangiomatosis (MA) es una lesión benigna intracraneal poco frecuente. La mayoría de los casos son aislados, pero también se han descrito casos asociados a Neurofibromatosis (NF) tipo 2. Los casos asociados a NF suelen ser asintomáticos. Los casos no asociados a NF son sintomáticos, se presentan en niños y adultos jóvenes, y en general afectan a leptomeninge y a corteza cerebral subyacente.</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">En este trabajo se describen 2 casos no asociados a NF en niños de 1 y 7 años de edad, que se manifestaron por crisis, las cuales desaparecieron tras la extirpación de la lesión. Histológicamente las lesiones eran de predominio celular en un caso y de predominio fibro-hialino en el otro.</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">De la revisión de la literatura se concluye que las meningioangiomatosis no asociadas a NF suelen ser lesiones únicas, clínicamente suelen presentarse con crisis convulsivas, y pueden verse asociadas a otras patologías, fundamentalmente a meningiomas.</p><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Histológicamente las lesiones corresponden a una proliferación celular de hábito meningotelial que se dispone alrededor de los vasos corticales. A pesar de que todos los casos tienen características comunes, existe un amplio espectro de formas histológicas, que abarca desde casos más celulares hasta casos más fibrosos con calcificaciones. Estas diferencias podrían corresponder a diferentes estadios evolutivos de la lesión. La extirpación de la lesión conlleva la desaparición de los síntomas.</p>" ] "en" => array:2 [ "titulo" => "Summary" "resumen" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Meningioangiomatosis (MA) is a rare benign intracraneal lesion. The majority of cases are sporadic although the association of this lesion with familial neurofibromatosis (NF) type 2 is well known. NF-associated MA may be multifocal and is often asymptomatic and diagnosed at autopsy. Non-associated cases are usually symptomatic, occurs in children and young adults and frequently arise in leptomeninges and underlying cerebral cortex.</p><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">In the present work, we describe two new non-associated cases of MA in two boys, seven and one year old with seizures that disappeared after surgical excision.</p><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Histopathologically, the lesion was predominantly cellular in one case and more fibrous in the other.</p><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">From the literature review we concluded that sporadic cases present as single lesions which manifest by seizures or persistent headaches. Rarely MA has been described to coexist with meningiomas.</p><p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Histopathologically, MA is characterized by a plaque-like proliferation of meningothelial and fibroblast- like cells surrounding small vessels and trapping islands of gliotic cortical tissue. The lesion does not show significant atypia, mitosis or necrosis. Although all cases of MA share unifying features, there are different degrees of histological presentation with cases predominantly cellular and others more fibrous and calcified. This could correspond to different stages in the evolution of the MA. Symptoms disappear with the complete excision of the lesion.</p>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara">Suárez-Gauthier, A.; Gómez de la Bárcena, M.R.; García-García, E.; Hinojosa, J.; Ricoy, J.R.: Meningioangiomatosis. Descripción de dos casos y revisión de la literatura. Neurocirugía 2006; 17: 250–254.</p>" ] ] "bibliografia" => array:2 [ "titulo" => "Bibliografía" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:35 [ 0 => array:3 [ "identificador" => "bib1" "etiqueta" => "1." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Case of the month: A 7 years old girl with seizures" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "H. Al-Hindi" 1 => "B. Subach" 2 => "R.L. Hamilton" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Brain Pathol" "fecha" => "1997" "volumen" => "7" "paginaInicial" => "1023" "paginaFinal" => "1024" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9217981" "web" => "Medline" ] ] ] ] ] ] ] ] 1 => array:3 [ "identificador" => "bib2" "etiqueta" => "2." 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| año/Mes | Html | Total | |
|---|---|---|---|
| 2023 Marzo | 0 | 2 | 2 |
| 2018 Marzo | 1 | 0 | 1 |
| 2018 Febrero | 25 | 9 | 34 |
| 2018 Enero | 30 | 11 | 41 |
| 2017 Diciembre | 25 | 21 | 46 |
| 2017 Noviembre | 44 | 19 | 63 |
| 2017 Octubre | 24 | 7 | 31 |
| 2017 Septiembre | 30 | 9 | 39 |
| 2017 Agosto | 32 | 5 | 37 |
| 2017 Julio | 33 | 7 | 40 |
| 2017 Junio | 40 | 6 | 46 |
| 2017 Mayo | 56 | 7 | 63 |
| 2017 Abril | 29 | 6 | 35 |
| 2017 Marzo | 47 | 14 | 61 |
| 2017 Febrero | 19 | 7 | 26 |
| 2017 Enero | 26 | 6 | 32 |
| 2016 Diciembre | 61 | 8 | 69 |
| 2016 Noviembre | 74 | 9 | 83 |
| 2016 Octubre | 71 | 8 | 79 |
| 2016 Septiembre | 106 | 15 | 121 |
| 2016 Agosto | 71 | 14 | 85 |
| 2016 Julio | 44 | 12 | 56 |
| 2016 Marzo | 6 | 0 | 6 |
| 2015 Diciembre | 4 | 0 | 4 |
| 2015 Agosto | 7 | 0 | 7 |
| 2015 Julio | 1 | 8 | 9 |
| 2015 Junio | 21 | 9 | 30 |
| 2015 Mayo | 35 | 11 | 46 |
| 2015 Abril | 32 | 12 | 44 |
| 2015 Marzo | 27 | 13 | 40 |
| 2015 Febrero | 17 | 9 | 26 |
| 2015 Enero | 28 | 8 | 36 |
| 2014 Diciembre | 21 | 12 | 33 |
| 2014 Noviembre | 21 | 11 | 32 |
| 2014 Octubre | 38 | 15 | 53 |
| 2014 Septiembre | 36 | 11 | 47 |
| 2014 Agosto | 42 | 11 | 53 |
| 2014 Julio | 34 | 9 | 43 |
| 2014 Junio | 59 | 14 | 73 |
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| 2014 Abril | 155 | 9 | 164 |
| 2014 Marzo | 374 | 18 | 392 |
| 2014 Febrero | 18 | 14 | 32 |
| 2014 Enero | 17 | 14 | 31 |
| 2013 Diciembre | 23 | 15 | 38 |
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| 2013 Octubre | 31 | 13 | 44 |
| 2013 Septiembre | 19 | 14 | 33 |
| 2013 Agosto | 31 | 19 | 50 |
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| 2013 Abril | 13 | 8 | 21 |
| 2013 Marzo | 15 | 16 | 31 |
| 2013 Febrero | 11 | 10 | 21 |
| 2013 Enero | 18 | 8 | 26 |
| 2012 Diciembre | 5 | 15 | 20 |
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| 2012 Octubre | 0 | 1 | 1 |
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