The Loss of 1p as a Reliable Marker of Progression in a Child with Aggressive Meningioma: A 16-Year Follow-Up Case Report.

Hemmer, Sina; Sippl, Christoph; Sahm, Felix; Oertel, Joachim; Urbschat, Steffi; Ketter, Ralf

Hemmer, Sina; Sippl, Christoph; Sahm, Felix; Oertel, Joachim; Urbschat, Steffi; Ketter, Ralf.

Afiliación

Hemmer S; Department of Neurosurgery, Faculty of Medicine, University of Saarland, Homburg/Saar, Germany.
Sippl C; Department of Neurosurgery, Faculty of Medicine, University of Saarland, Homburg/Saar, Germany.
Sahm F; Institute of Neuropathology, Faculty of Medicine, University of Heidelberg, Heidelberg, Germany.
Oertel J; Department of Neurosurgery, Faculty of Medicine, University of Saarland, Homburg/Saar, Germany.
Urbschat S; Department of Neurosurgery, Faculty of Medicine, University of Saarland, Homburg/Saar, Germany.
Ketter R; Department of Neurosurgery, Faculty of Medicine, University of Saarland, Homburg/Saar, Germany, ralf.ketter@uks.eu.

Pediatr Neurosurg ; 55(6): 418-425, 2020.

Article en En | MEDLINE | ID: mdl-33296905

Asunto(s)

Neoplasias Meníngeas; Meningioma; Adulto; Niño; Femenino; Estudios de Seguimiento; Humanos; Neoplasias Meníngeas/diagnóstico por imagen; Neoplasias Meníngeas/genética; Neoplasias Meníngeas/cirugía; Meningioma/genética; Meningioma/cirugía; Monosomía; Recurrencia Local de Neoplasia

Palabras clave

Chromosomes; Deletion of 1p; Genetic progression; Meningioma; SMO and AKT1 mutations

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Meníngeas / Meningioma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Child / Female / Humans Idioma: En Revista: Pediatr Neurosurg Asunto de la revista: NEUROCIRURGIA / PEDIATRIA Año: 2020 Tipo del documento: Article País de afiliación: Alemania

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