Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Frontoparietal Craniotomy"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 15, Iss 9, Pp XD01-XD02 (2021)
The Central Neurocytoma (CN) is a rare tumour of brain which is commonly seen in young adults. Two cases, A 24-year-old-male and a 37-year-old-female with CN of the lateral ventricles are reported here. Both patients presented with complaints of hea
Externí odkaz:
https://doaj.org/article/07c1d94c4b274f6bb21b78a6cb5210f5
Autor:
Jordan M. Komisarow, Jenna S. Hynes, Eric W. Sankey, Courtney Mitchell, Andrew S. Griffin, Jake Maule, Allan H. Friedman, Sarah K. Dotters-Katz
Publikováno v:
Journal of Neurosurgery. 134:189-196
Intravascular papillary endothelial hyperplasia (IPEH), commonly known as Masson’s tumor, is a benign lesion that manifests as an excessive proliferation of endothelial cells within a vessel wall. IPEH is extremely rare in the brain, with only 36 i
Autor:
Xun Qin, Ju-Xiang Chen, Guanghui Li, Sheng-Qing Lv, Yan Xiang, Yao Li, Lin Yang, Zuo-Xin Zhang, Bao-Zhong Shi
Publikováno v:
Chinese Neurosurgical Journal
Chinese Neurosurgical Journal, Vol 7, Iss 1, Pp 1-7 (2021)
Chinese Neurosurgical Journal, Vol 7, Iss 1, Pp 1-7 (2021)
Background Multifocal glioblastoma is a rare type of glioblastoma with worse prognosis. In this article, we aimed to report two cases of classical multifocal glioblastoma. Case presentation In case 1, a 47-year-old male presented with dizziness, and
Publikováno v:
Surgical Neurology International
Background: Traumatic acute epidural hematomas (EDHs) commonly develop by rupture of the meningeal arteries. EDH caused by an injury of the diploic channel (DC) has not been reported. Case Description: A 21-year-old man suffered a head injury while f
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-5 (2020)
Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-5 (2020)
Background Chronic calcified subdural empyema is an exceedingly rare central nervous system infection with a handful of cases published to date. Reported cases presented with nonspecific clinical signs and symptoms. The duration between the initial o
Primary delayed onset craniosynostosis in a child demonstrated by serial computed tomography imaging
Publikováno v:
International Journal of Oral and Maxillofacial Surgery. 45:1347-1350
Primary delayed onset craniosynostosis is a rarely reported phenomenon. The unique case of a 2-year-old boy who had computed tomography (CT) scans performed 20 months apart demonstrating the post-gestational development of sagittal suture craniosynos
Publikováno v:
British journal of neurosurgery.
Introduction: We report a rare case of skull deformity in a child with shunted hydrocephalus. Case report: A 2.5-year-old boy with a history of cerebral palsy (CP), shunted hydrocephalus and seizures was admitted to our children's hospital with statu
Publikováno v:
CNS Oncology
Astroblastoma is an uncommon neuroepithelial primary tumor of the brain which is of uncertain origin. We present a case of high-grade astroblastoma in an 18-year-old female with a severe headache, loss of appetite, vomiting and generalized weakness.
Publikováno v:
Journal of Neurosciences in Rural Practice
Journal of Neurosciences in Rural Practice, Vol 08, Iss 01, Pp 140-142 (2017)
Journal of Neurosciences in Rural Practice, Vol 8, Iss 1, Pp 140-142 (2017)
Journal of Neurosciences in Rural Practice, Vol 08, Iss 01, Pp 140-142 (2017)
Journal of Neurosciences in Rural Practice, Vol 8, Iss 1, Pp 140-142 (2017)
Lipomatous meningiomas are extremely rare subtypes of benign meningiomas and are classified as metaplastic meningioma in the World Health Organization classification. We present a 77-year-old man presented with the history of a gradually intensifying
Publikováno v:
World neurosurgery. 118
Primary intracranial chondrosarcoma is an extremely rare malignant tumor of the central nervous system, which accounts for0.16% of all primary intracranial tumors. This rare tumor has a high associated morbidity from the tumor itself as well as from