Results 1 to 10 of about 54,777 (293)

Location, length, and enhancement: systematic approach to differentiating intramedullary spinal cord lesions [PDF]

open access: yesInsights into Imaging, 2018
Purpose Intramedullary spinal cord abnormalities are often challenging to diagnose. Spinal cord biopsy is a high-risk procedure with the potential to cause permanent neurological injury.
Sarah Mohajeri Moghaddam, Alok A. Bhatt
doaj   +2 more sources

Stereotactic Radiation for Treating Primary and Metastatic Neoplasms of the Spinal Cord

open access: yesFrontiers in Oncology, 2020
Stereotactic radiation treatment can be used to treat spinal cord neoplasms in patients with either unresectable lesions or residual disease after surgical resection.
Elisa K. Liu   +4 more
doaj   +3 more sources

Right Upper Lobe Pulmonary Spindle Cell Neoplasm With Rhabdoid Differentiation and Spinal Canal Invasion in a 19‐Year‐Old Female: A Case Report [PDF]

open access: yesClinical Case Reports
We present an unusual case involving a 19‐year‐old female with progressive respiratory distress. Testing revealed pulmonary spindle cell neoplasms with rhabdoid features and spinal cord involvement and infectious complications, emphasizing the importance
Quang Dai La   +7 more
doaj   +2 more sources

A Technical Problem in Diagnosis Clarity of Solitary Spinal Cord Neurofibroma in an Eleven-month-old Boy [PDF]

open access: yesFolia Medica, 2017
Spinal neurofibroma is one of the rarest of the neoplasms involving the spinal cord or roots and occurs much less often than neurinoma, meningioma or glioma. The sixth pediatric case of solitary intramedullary tumor was described in 2013, according to B.
Poriazova Elena G.   +6 more
doaj   +4 more sources

Near-miss Thoracic Spine Solitary Plasmacytoma with Neurological Deficit during Pregnancy: A Case Report [PDF]

open access: yesMalaysian Orthopaedic Journal, 2022
Solitary plasmacytoma (SPC) account for only 5% of plasma cell neoplasms, and the literature hardly reports spinal SPC with a neurological deficit.
Teh KH   +4 more
doaj   +1 more source

Multiple ossified intracranial and spinal meningiomas: a rare case report and literature review

open access: yesFrontiers in Neurology, 2023
Ossified intracranial meningiomas (OIM) and ossified spinal meningiomas (OSM) are rare neoplasms of mesenchymal origin that predominantly manifest in the spinal cord and infrequently in the cranial region, accounting for ~0. 7–5.5% of all meningiomas. It
Jian Wang   +8 more
doaj   +1 more source

A case of primary intramedullary tumor [PDF]

open access: yesRomanian Journal of Neurology, 2016
Primary spinal cord tumors are rare neoplasms that can lead to significant patient disability and mortality. Given their rarity, they are often misdiagnosed, especially in the early stages, when a high index of suspicion is required.
Florin Scarlatescu
doaj   +1 more source

Salvage carbon ion radiotherapy for recurrent solitary fibrous tumor: A case report and literature review

open access: yesJournal of Orthopaedic Surgery, 2020
Background: Malignant solitary fibrous tumor (MSFT) arising from the spinal cord is extremely rare and poorly understood mesenchymal neoplasms: only a few MSFT in the spinal canal has been described.
Kazuma Murata   +12 more
doaj   +1 more source

Intracranial Metastases Originating From Pediatric Primary Spinal Cord Glioblastoma Multiforme: A Case Report and Literature Review

open access: yesFrontiers in Oncology, 2020
Primary spinal cord glioblastoma multiforme (scGBM) is an uncommon entity in pediatrics, and intracranial metastasis originating in spinal cord gliomas is very rare.
Dengpan Song   +4 more
doaj   +1 more source

An Unusual Presentation of Spinal Giant Cell Glioblastoma in a 21-Year-Old Female

open access: yesJournal of Investigative Medicine High Impact Case Reports, 2019
Primary spinal cord giant cell glioblastoma multiforme of the thoracic spinal cord is a rarely-diagnosed primary spinal cord tumor in comparison to neoplasms in intracranial locations.
Benjamin J. Delgado BS   +6 more
doaj   +1 more source

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