Cargando…

Retrospective Multicentric Study on Non-Optic CNS Tumors in Children and Adolescents with Neurofibromatosis Type 1

The natural history of non-optic central nervous system (CNS) tumors in neurofibromatosis type 1 (NF1) is largely unknown. Here, we describe prevalence, clinical presentation, treatment, and outcome of 49 non-optic CNS tumors observed in 35 pediatric patients (0–18 years). Patient- and tumor-related...

Descripción completa

Detalles Bibliográficos
Autores principales:	Santoro, Claudia, Picariello, Stefania, Palladino, Federica, Spennato, Pietro, Melis, Daniela, Roth, Jonathan, Cirillo, Mario, Quaglietta, Lucia, D’Amico, Alessandra, Gaudino, Giuseppina, Meucci, Maria Chiara, Ferrara, Ursula, Constantini, Shlomi, Perrotta, Silverio, Cinalli, Giuseppe
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353051/ https://www.ncbi.nlm.nih.gov/pubmed/32486389 http://dx.doi.org/10.3390/cancers12061426

Ejemplares similares

Medullary unidentified bright objects in Neurofibromatosis type 1: a case series
por: D’Amico, Alessandra, et al.
Publicado: (2018)

Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?
por: Santoro, Claudia, et al.
Publicado: (2018)

Multimodal evaluation of the cerebrovascular reserve in Neurofibromatosis type 1 patients with Moyamoya syndrome
por: D’Amico, Alessandra, et al.
Publicado: (2020)

Posterior Fossa Tumours in the First Year of Life: A Two-Centre Retrospective Study
por: Picariello, Stefania, et al.
Publicado: (2022)

Diencephalic Syndrome Due to Optic Pathway Gliomas in Pediatric Patients: An Italian Multicenter Study
por: De Martino, Lucia, et al.
Publicado: (2022)

Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1
por: Santoro, Claudia, et al.
Publicado: (2018)

DDEL-03. The use of programmable valves as a vehicle for intrathecal chemotherapy delivery in infants with CNS tumors and hydrocephalus.
por: Dvir, Rina, et al.
Publicado: (2022)

Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype–Phenotype Correlations
por: Peduto, Cristina, et al.
Publicado: (2023)

Extra-neural metastases in pediatric diffuse midline gliomas, H3 K27-altered: presentation of two cases and literature review
por: De Martino, Lucia, et al.
Publicado: (2023)

Removal of Koos IV acoustic neuroma and auditory brainstem implant in NF2 patient
por: Scala, Maria Rosaria, et al.
Publicado: (2021)

Symptomatic malignant spinal cord compression in children: a single-center experience
por: De Martino, Lucia, et al.
Publicado: (2019)

Bone metabolism in patients with type 1 neurofibromatosis: key role of sun exposure and physical activity
por: Ferrara, Ursula Pia, et al.
Publicado: (2022)

The effect of parental age on the presence of de novo mutations – Lessons from neurofibromatosis type I
por: Dubov, Tom, et al.
Publicado: (2016)

An update on the CNS manifestations of neurofibromatosis type 2
por: Coy, Shannon, et al.
Publicado: (2019)

Correction to: An update on the CNS manifestations of neurofibromatosis type 2
por: Coy, Shannon, et al.
Publicado: (2019)

Sudden unexpected nocturnal death in Chiari type 1 malformation and potential role of opioid analgesics
por: Jonathan, Roth, et al.
Publicado: (2014)

Role, function and challenges of multidisciplinary centres for rare diseases exemplified for neurofibromatosis type 1 syndrome
por: Toledano-Alhadef, Hagit, et al.
Publicado: (2020)

Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders
por: Giugliano, Teresa, et al.
Publicado: (2019)

The Clinical and Prognostic Impact of the Choice of Surgical Approach to Fourth Ventricular Tumors in a Single-Center, Single-Surgeon Cohort of 92 Consecutive Pediatric Patients
por: Onorini, Nicola, et al.
Publicado: (2022)

Endoscopic considerations treating hydrocephalus caused by basal ganglia and large thalamic tumors
por: Roth, Jonathan, et al.
Publicado: (2015)

Over-drainage and persistent shunt-dependency in patients with idiopathic intracranial hypertension treated with shunts and bariatric surgery
por: Roth, Jonathan, et al.
Publicado: (2015)

Occipital interhemispheric transtentorial approach to a pineoblastoma in a 4-year-old child
por: Imperato, Alessia, et al.
Publicado: (2021)

Removal of a thoracic intramedullary epidermoid tumor in a child
por: Costanzo, Marianna Di, et al.
Publicado: (2023)

Neuropsychiatric Manifestations, Reduced Self-Esteem and Poor Quality of Life in Children and Adolescents with Neurofibromatosis Type 1 (NF1): The Impact of Symptom Visibility and Bullying Behavior
por: Cavallo, Nicola Davide, et al.
Publicado: (2023)

Acute subdural hematomas in shunted normal-pressure hydrocephalus patients – Management options and literature review: A case-based series
por: Berger, Assaf, et al.
Publicado: (2018)

Cavum trigeminale cephalocele associated with intracranial hypertension in an 18-month-old child: illustrative case
por: Miccoli, Giovanni, et al.
Publicado: (2021)

Illustrated dynamic stories behind pediatric neurosurgery
por: Rochanaroon, Voramol, et al.
Publicado: (2019)

Malignant cerebral infarction associated with COVID-19 in a child
por: Scala, Maria Rosaria, et al.
Publicado: (2021)

Interhemispheric transcallosal transchoroidal approach to a pineal teratoma in a 15-year-old boy
por: Cinalli, Giuseppe, et al.
Publicado: (2021)

Acute ischemic stroke secondary to ventriculoperitoneal shunt dysfunction in a child with Moyamoya syndrome
por: Vitulli, Francesca, et al.
Publicado: (2022)

HGG-04. Intramedullary spinal high grade glioma with ALK fusion and excellent response to targeted treatment with alectinib: case report
por: Dvir, Rina, et al.
Publicado: (2022)

Endoscopic ultrasonic resection of calcified tumor of the third ventricle
por: Spennato, Pietro, et al.
Publicado: (2023)

Isoform-specific NF1 mRNA levels correlate with disease severity in Neurofibromatosis type 1
por: Assunto, Antonia, et al.
Publicado: (2019)

Caveats for Using Shock Tube in Blast-Induced Traumatic Brain Injury Research
por: Chen, Yun, et al.
Publicado: (2013)

Phacomatoses in the pediatric age group
por: Constantini, Shlomi, et al.
Publicado: (2020)

Cutaneous Findings in Neurofibromatosis Type 1
por: Ozarslan, Bengisu, et al.
Publicado: (2021)

Precocious Pseudo-Puberty in a 7-Year-Old Girl Due to Malignant Mixed Ovarian Germ Cell Tumor
por: Improda, Nicola, et al.
Publicado: (2023)

Prenatal diagnosis and postnatal management of congenital unilateral hydrocephalus for stenosis of the foramen of Monro
por: Spennato, Pietro, et al.
Publicado: (2021)

MBCL-17. METASTATIC MEDULLOBLASTOMA CAN BE CURED WITHOUT EXCISION OF THE PRIMARY TUMOR: A SINGLE CENTER EXPERIENCE
por: Dvir, Rina, et al.
Publicado: (2020)

SDPS-25 COMPARISON OF MOLECULAR ALTERATIONS BETWEEN SYSTEMIC AND CNS METASTATIC SITES REVEALSMUTATIONAL DISCORDANCES
por: Huang, David, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_k2cnvtvgoohd32ledaqsq2gr19