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megalencephaly/náusea
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Supraorbital Keyhole Microsurgical Fenestration of Symptomatic Temporal Arachnoid Cysts in Children: Advantages and Limitations.
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OBJECTIVE
To investigate the impact of endoscope-assisted microsurgical fenestration on temporal arachnoid cysts, and to determine the advantages and limitations of the technique.
METHODS
Twenty-five children with symptomatic temporal arachnoid cysts were operated via eyebrow supraorbital keyhole
Presenting symptoms of pediatric brain tumors diagnosed in the emergency department.
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OBJECTIVE
The primary objective of this study is to categorize the symptoms associated with brain tumors as diagnosed in the emergency department (ED). The secondary objective is to detail the specific characteristics of these headaches via a subgroup analysis.
METHODS
A retrospective chart review
Lhermitte-Duclos disease with neurofibrillary tangles in heterotopic cerebral grey matter.
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Lhermitte-Duclos disease (LDD), a disorder first described by French physicians Lhermitte and Duclos in 1920 [25], is a benign, slow growing dysplastic gangliocytoma of the cerebellum, characterized by replacement of the granule cell layer by abnormal granule and Purkinje like cells. The most
Glutaric aciduria type II [corrected] and brain tumors: a case report and review of the literature.
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Heritable diseases associated with childhood tumors are sometimes defined as a probable etiologic factor or a coincidence. First of all, we must know the actual number of patients. Herein a case with medulloblastoma associated with glutaric aciduria type II [corrected] is reported for this purpose.
Presentation of childhood CNS tumours: a systematic review and meta-analysis.
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BACKGROUND
Suspicion of a CNS tumour is classically raised by symptoms of raised intracranial pressure, focal deficits (including seizures), or papilloedema. Development of guidelines is needed for the identification and referral of children who might have a CNS tumour. We did a systematic
Primary disseminated leptomeningeal oligodendroglioma with 1p deletion. Case report.
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The authors report the case of a 2-year-old boy with a primary, diffuse leptomeningeal oligodendroglioma in which the deletion of chromosome arm lp was identified by performing a fluorescence in situ hybridization (FISH) analysis. This previously healthy child initially presented with malaise,
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