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| http://dx.doi.org/10.4322/acr.2021.348 | DOI Listing |
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Congenital extraventricular neurocytoma with atypical features in a 3-day-old neonate.
Childs Nerv Syst
December 2024
Department of Neurosurgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Extraventricular neurocytoma (EVN) is a rare neuronal tumor with a marked tendency towards ganglionic or glial differentiation. Although EVN commonly occurs in young adults, congenital cases are extremely rare, and standardized therapeutic strategies remain undetermined. The presence of atypical features such as increased mitotic activity on histological analysis is correlated with a higher rate of recurrence and poor prognosis.
View Article and Find Full Text PDFCase report: A rare case of neurocytoma of the Vth cranial nerve.
Front Oncol
September 2024
Department of Neurosurgery, Ji'an Central People's Hospital, Ji'an, China.
We report a case of neurocytoma originating from cranial nerve V. A 53-year-old female patient presented with a 20-day history of right frontotemporal facial paresthesia and pain. Magnetic resonance imaging (MRI) showed a 2.
View Article and Find Full Text PDFExtraventricular Neurocytoma of the Sellar Region Presenting With Syndrome of Inappropriate Antidiuresis.
JCEM Case Rep
September 2024
Neuroendocrinology Research Center, Endocrinology Section, Medical School and Hospital Universitário Clementino Fraga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-617, Brazil.
Neurocytomas are neuronal tumors that are usually intraventricular. Rare cases can arise from extraventricular sites. To our knowledge, only 29 cases of extraventricular neurocytoma of the sellar region (EVNSR) have been reported in the literature.
View Article and Find Full Text PDFTumor-Agnostic Genomic and Clinical Analysis of BRAF Fusions Identifies Actionable Targets.
Clin Cancer Res
September 2024
Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Purpose: Even though BRAF fusions are increasingly detected in standard multigene next-generation sequencing panels, few reports have explored their structure and impact on clinical course.
Experimental Design: We collected data from patients with BRAF fusion-positive cancers identified through a genotyping protocol of 97,024 samples. Fusions were characterized and reviewed for oncogenic potential (in-frame status, non-BRAF partner gene, and intact BRAF kinase domain).
Clinical rarity: simultaneous choroid plexus papilloma and extraventricular neurocytoma presenting as intraventricular hemorrhage in an adolescent.
J Surg Case Rep
January 2024
Department of Neurosurgery, Children's Hospital of New Orleans, New Orleans, LA, United States.
We present a patient with an intraventricular hemorrhage. Imaging identified a left atrial intraventricular mass and a vague adjacent second periventricular cystic lesion. A guided trans-sulcal approach via a left parietal craniotomy resulted in a gross total resection of both lesions.
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