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94 results on '"García Allut, Alfredo"'

13. Quiste aracnoideo gigante

Author

González Gómez, Lara, primary, Román Pena, Paula, additional, Serramito García, Ramón, additional, Gelabert González, Miguel, additional, and García Allut, Alfredo, additional

Published
2016
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16. Linfoma primario de la calota craneal

Author

Prieto González, Angel, Reyes Santías, Rosa María, Santín Amo, José María, García Allut, Alfredo, Gelabert González, Miguel, Castro Bouzas, Daniel, and Serramito García, Ramón

Published
2011

21. Hematoma subdural crónico en pacientes jóvenes

Author

Gelabert-González, Miguel, primary, Frieiro-Dantas, Carla, additional, Serramito-García, Ramón, additional, Díaz-Cabanas, Lucía, additional, Aran-Echabe, Eduardo, additional, Rico-Cotelo, María, additional, and García-Allut, Alfredo, additional

Published
2013
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24. Control de las crisis epilépticas durante el postoperatorio inmediato de los tumores cerebrales supratentoriales: recomendaciones del Grupo de Neurocirugía Funcional y Estereotáctica de la Sociedad Española de Neurocirugía

Author

Domínguez-Páez, Miguel, primary, Herranz-Fernández, José Luis, additional, Villanueva-Haba, Vicente, additional, Sánchez-Álvarez, Juan Carlos, additional, Olivares-Granados, Gonzalo, additional, Sola, Rafael García-de, additional, Albisua-Sánchez, Julio, additional, Arráez-Sánchez, Miguel Ángel, additional, Mosqueira-Centurión, Bernardo, additional, Amaro-Cendón, Santiago, additional, Bollar-Zabala, Alicia, additional, Carceller-Benito, Fernando, additional, Salazar-Hernández, Julio, additional, Fernández-Carballal, Carlos, additional, García-Allut, Alfredo, additional, García-Navarrete, Eduardo, additional, Gutiérrez-Martín, Antonio, additional, Lara-Cantalejo, José Luis, additional, Márquez-Rivas, Javier, additional, Oliver-Abadal, Bartolomé, additional, Pomposo-Gaztelu, I.ñigo, additional, Prieto-González, Ángel, additional, Rumiá-Arboix, Jordi, additional, and Úrculo-Bareño, Enrique, additional

Published
2012
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26. Linfoma primario de la calota craneal

Author

Castro Bouzas, Daniel, primary, Prieto González, Ángel, additional, Serramito García, Ramón, additional, Santín Amo, José María, additional, Reyes Santías, Rosa María, additional, García Allut, Alfredo, additional, and Gelabert González, Miguel, additional

Published
2011
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28. Tumores de la vaina de las raíces nerviosas espinales

Author

Gelabert González, Miguel, primary, Castro Bouzas, Daniel, additional, Serramito García, Ramón, additional, Santín Amo, José María, additional, Arán Echabe, Eduardo, additional, Prieto González, Ángel, additional, and García Allut, Alfredo, additional

Published
2011
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29. Gangliocitoma hipofisario no funcionante

Author

Andújar-Plata, Paula, primary, Cabezas-Agrícola, José Manuel, additional, Rivero-Luis, María Teresa, additional, Becerra, Eugenio Pérez-, additional, García-Allut, Alfredo, additional, and Casanueva, Felipe F., additional

Published
2011
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39. Tumores de plexos coroideos

Author

Gelabert González, Miguel, primary, Fernández Villa, Juan Manuel, additional, López García, Elena, additional, González García, Jesús, additional, and García Allut, Alfredo, additional

Published
2001
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40. Ependimomas intracraneales

Author

Gelabert González, Miguel, primary, García Allut, Alfredo, additional, Fernández Villa, Juan Manuel, additional, González García, Jesús, additional, and Martínez Rumbo, Ramón, additional

Published
2001
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43. Hematoma epidural cervical espontáneo

Author

González García, Jesús, primary, Gelabert González, Miguel, additional, García Allut, Alfredo, additional, Fernández Villa, Juan Manuel, additional, López García, Elena, additional, and García Pravos, Antonio, additional

Published
2000
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46. Desarrollo «de novo»de un quiste aracnoideo supraselar

Author

Gelabert-González, Miguel, Pita-Buezas, Lara, Santín-Amo, José María, Román-Pena, Paula, Serramito-García, Ramón, and García-Allut, Alfredo

Abstract

Los quistes aracnoideos (QA) intracraneales son lesiones quísticas formados a partir de las aracnoides y que tienen una prevalencia entre el 1-2% en la población pediátrica. Presentamos el caso clínico de un niño de 2 años que presentó inestabilidad para la marcha y episodios de desviación ocular; al nacimiento se le había realizado una ecografía transfontanelar que fue normal. Se le practicó una tomografía computarizada (TC) y resonancia magnética (RM) que evidenciaron un quiste aracnoideo supraselar acompañado de importante hidrocefalia. Se realizó una fenestración endoscópica del quiste con remisión completa de la sintomatología.

Published
2015
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47. Solitary fibrous tumour/haemangiopericytoma of the spinal cord.

Author

Flores-Justa A, López-García E, García-Allut A, and Reyes-Santías RM

Subjects
Biomarkers, Tumor analysis, Decompression, Surgical, Diagnostic Errors, Female, Hemangiopericytoma chemistry, Hemangiopericytoma complications, Hemangiopericytoma diagnostic imaging, Humans, Laminectomy, Lumbar Vertebrae surgery, Magnetic Resonance Imaging, Meningeal Neoplasms diagnosis, Meningioma diagnosis, Middle Aged, Neuroimaging, Paraplegia etiology, Solitary Fibrous Tumors chemistry, Solitary Fibrous Tumors complications, Solitary Fibrous Tumors diagnostic imaging, Somatosensory Disorders etiology, Spinal Cord Neoplasms chemistry, Spinal Cord Neoplasms complications, Spinal Cord Neoplasms diagnostic imaging, Spinal Fusion, Spinal Stenosis surgery, Surgery, Computer-Assisted, Thoracic Vertebrae, Ultrasonography, Interventional, Hemangiopericytoma surgery, Solitary Fibrous Tumors surgery, Spinal Cord Neoplasms surgery
Abstract

Solitary fibrous tumours/haemangiopericytomas (SFT/HPC) are fibroblastic mesenchymal neoplasms that harbour a genetic fusion of NAB2/STAT6. There are few reported cases in the central nervous system (CNS), of which spinal tumours are minority. We present a case of a 63-year-old woman with progressive paraparesis and a sensory level of T6. On the MRI we detected an intradural extramedullary lesion on T9-T10. We performed a laminectomy with an intraoperative ultrasound study in which we observed a heterogeneous lesion with an infiltrating pattern affecting the medulla at several points, and resection of the lesion. Immunohistological findings revealed positivity for vimentin, CD34 and STAT6; Ki-67 was 2%. A final diagnosis of SFT/HPC with SFT phenotype was made. SFT/HPC of the CNS is a rare neoplasm that should be taken into account in the differential diagnosis of these kinds of lesions, as clinical and MRI findings often lead to errors in diagnostic approach. The support of intraoperative ultrasound can assist in surgical decision-making., (Copyright © 2018 Sociedad Española de Neurocirugía. Publicado por Elsevier España, S.L.U. All rights reserved.)

Published
2018
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48. [Cerebral infarction after pituitary apoplexy: Description of a case and review of the literature].

Author

Serramito García R, Santín Amo JM, Román Pena P, Pita Buezas L, González Gómez L, and García Allut A

Subjects
Adenoma, Adult, Brain Ischemia, Female, Humans, Pituitary Neoplasms, Cerebral Infarction etiology, Pituitary Apoplexy complications
Abstract

Pituitary apoplexy is usually the result of hemorrhagic infarction in a pituitary adenoma. The clinical presentation varies widely and includes asymptomatic cases, classical pituitary apoplexy and even sudden death. Cerebral ischemia due to pituitary apoplexy is very rare. It may be caused by vasospasm or direct compression of cerebral vessels by the tumor. We report a case of pituitary apoplexy associated with cerebral infarction and discuss the relationship between the two events., (Copyright © 2016 Sociedad Española de Neurocirugía. Publicado por Elsevier España, S.L.U. All rights reserved.)

Published
2016
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49. [Bilateral chronic subdural haematoma: Analysis of a series of 190 patients].

Author

Gelabert-González M, Arán-Echabe E, Bandín-Diéguez FJ, Santín-Amo JM, Serramito-García R, Prieto-González Á, and García-Allut A

Subjects
Adolescent, Adult, Aged, Aged, 80 and over, Female, Hematoma, Subdural, Chronic pathology, Humans, Male, Middle Aged, Retrospective Studies, Young Adult, Hematoma, Subdural, Chronic surgery
Abstract

Objective: The aim of this study is to analyse the clinical findings and surgical results in a series of patients with bilateral chronic subdural haematoma (BCSDH), and compare the results with a series of patients treated for unilateral chronic subdural haematoma (UCSDH)., Patients and Methods: A retrospective study was performed on 1523 patients diagnosed and surgically treated for chronic subdural haematoma over a period of 30 years. Patients were divided into 2 groups: The study group consisting of 190 patients operated on for a BCSDH and the control group consisting of patients operated on for an UCSDH (1333 cases)., Results: The patient series included 126 males (66.3%) and 64 females (33.7%), with a mean age at diagnosis of 74.8±10.2. The control group consisted of 870 males (65.2%) and 463 women (34.8%), with a mean age of 73.2±12.1. The most common presenting symptoms was cognitive impairment in 63 patients (33.2%) with BCSDH and 416 (29.5%) with UCSDH. Recurrence rates were 9.4% (18 patients) and 5.7% (77 patients) in unilateral and bilateral haematomas, respectively. The mortality was 10 patients (5.2%) with BCSDH and 55(4%) with UCSDH. Factors significantly related to recurrence in the univariate analysis were being male (P=.040), anticoagulant/antiplatelet therapy (P=.032), and poor neurological status at admission (P=.039)., Conclusions: This study indicates that BCSDH is more frequent in males, and the most common presentation is headache. The most important factors influencing recurrences are being male, intake of anticoagulant-antiaggregant drugs, and worse clinical status at admission., (Copyright © 2015 Sociedad Española de Neurocirugía. Published by Elsevier España. All rights reserved.)

Published
2016
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50. [Imaging diagnosis of arachnoid cysts].

Author

Gelabert-González M, Santín-Amo JM, Aran-Echabe E, and García-Allut A

Subjects
Diagnosis, Differential, Humans, Arachnoid Cysts diagnosis, Diagnostic Imaging
Abstract

Arachnoid cysts are malformed lesions that contain a fluid similar to the cerebrospinal fluid, and are usually located within the arachnoidal membrane. They represent 1% of all intracranial lesions, and in recent years, with the development of radiological techniques, the clinical detectability of arachnoid cysts seems to have increased. Although the majority of diagnosed arachnoid cysts are located in the cranial cavity and especially in the Sylvian fissure, a small number are located at spinal level and they can occur extra- or intra-spinally. An analysis is carried out, detailing the various tests used for the diagnosis of both intracranial and spinal arachnoids cysts, analysing the indications of each one depending on the location of the cysts and patient age., (Copyright © 2015 Sociedad Española de Neurocirugía. Published by Elsevier España. All rights reserved.)

Published
2015
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