Results 21 to 30 of about 63,554 (339)

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

Clinical reasoning in canine spinal disease: what combination of clinical information is useful? [PDF]

open access: yes, 2015
Spinal disease in dogs is commonly encountered in veterinary practice. Numerous diseases may cause similar clinical signs and presenting histories. The study objective was to use statistical models to identify combinations of discrete parameters from the
ABRAMSON   +36 more
core   +3 more sources

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

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   +1 more source

Spinal Cord Ependymomas [PDF]

open access: yes, 2009
Intradural or primary spinal cord tumors (SCT) are rare. However, when these lesions grow, compression of the spinal cord can lead to limb dysfunction, motor or sensory loss, and possibly death.
Blyzniuk, Carol, BSN, RN   +1 more
core   +2 more sources

Ancient Schwannoma of the Cauda Equina: our experience and review of the literature [PDF]

open access: yes, 2016
Ancient schwannomas (AS) are exceedingly rare variant of common schwannomas (CS). Only two cases involving the cauda equina region have been previously reported in literature.
Caruso, Riccardo   +5 more
core   +4 more sources

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

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   +1 more source

Lymphoma Spectrum of Image Findings and Mimics in One Patient.

open access: yesJournal of the Belgian Society of Radiology, 2023
Lymphoma is a malignancy arising from lymphocytes or lymphoblasts. Depending on organ involved, aggressiveness, and primary or secondary disease, the expression of lymphoma shows polymorphism and sometimes makes it difficult to diagnose from imaging ...
Kuan-Yu Lin   +2 more
doaj   +1 more source

Tumors in von Hippel–Lindau Syndrome: From Head to Toe—Comprehensive State-of-the-Art Review [PDF]

open access: yes, 2018
Von Hippel–Lindau syndrome (VHL) is an autosomal-dominant hereditary tumor disease that arises owing to germline mutations in the VHL gene, located on the short arm of chromosome 3.
Bhalla, Sanjeev   +6 more
core   +1 more source

An Hourglass-Type Spinal Schwannoma Spreading to the Chest Treated with One-Stage Total Removal through Posterior Paravertebral Approach without Opening the Pleural Cavity (Clinical Observation)

open access: yesActa Biomedica Scientifica, 2021
The article describes the treatment of a 20-year-old patient with a spinal hourglass schwannoma (neurinoma) in the thoracic spine, growing from the right Th3 spinal root, spreading into the thoracic cavity and compressing the apex of the right lung.
I. A. Vasilyev   +5 more
doaj   +1 more source

Home - About - Disclaimer - Privacy