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Dorsal Intradural Extramedullary Bronchogenic Cysts: A Case Report and Comprehensive Literature Review.
Cureus
December 2024
Neurological Surgery, High Specialty Regional Hospital Bajio, León, MEX.
Intradural extramedullary bronchogenic cysts (IEBCs) are exceedingly rare congenital entities, composed of respiratory epithelial cells derived from the anomalous development of the embryonic foregut. Due to their exceptionally low morbidity, only limited cases are available. Consequently, the clinical features and optimal therapeutic approach remain poorly understood.
View Article and Find Full Text PDFSpinal intradural malignant peripheral nerve sheath tumor at the foramen magnum in a non-neurofibromatosis child.
Childs Nerv Syst
December 2024
Department of Neurosurgery, Postgraduate Institute of Medical Education & Research (PGIMER), Sector 12, Chandigarh, 160012, India.
Primary spinal intradural malignant peripheral nerve sheath tumors (MPNSTs) are rare neoplasms, especially in children with a non-neurofibromatosis background. Scarce pediatric data exist with regard to such tumors. A 4-year-old child with a history of spastic limb weakness was operated for a foramen magnum spinal lesion (intradural and extradural) with imaging suggestive of schwannoma; the histopathology, however, was that of a MPNST.
View Article and Find Full Text PDFUnusual appearance of spontaneous spinal intradural hematoma mimicking a meningioma.
Radiol Case Rep
January 2025
King Saud bin Abdulaziz University for Health Sciences, College of Medicine, Riyadh Saudi Arabia.
Spontaneous spinal intradural hematoma is uncommon. It can mimic vascular or hemorrhagic neoplasms, as certain imaging features overlap. The distinction between spinal hematoma and neoplasm is crucial for the approach to management and might determine the outcome.
View Article and Find Full Text PDFSolitary intradural plasmacytomas are extremely rare. We present a case of a patient with headache and diagnosis of meningiomatosis. Onset symptoms were abrupt neurological deterioration and paraparesis.
View Article and Find Full Text PDFA rare coexistence of a non-dysraphic intradural lipoma and a cyst in the lumbar spine - A case report and literature review.
Int J Surg Case Rep
November 2024
Department of Neurosurgery, Tartous University, Tartous, Syrian Arab Republic.
Article Synopsis
- Spinal intradural lipomas are rare tumors, particularly when not linked to spinal dysraphism, and are often diagnosed late due to their gradual growth and location.
- A case involving an eight-year-old girl revealed a lipoma and a cyst in her lumbar region, leading to symptoms like limb weakness and urinary issues; both lesions were partially removed surgically with a successful recovery.
- The discovery of fluid-filled cysts alongside lipomas is extremely rare, and while the exact origin of these lipomas is unclear, their coexistence with cysts may prompt earlier detection and intervention.
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