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A 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.
Nondysraphic Intradural Spinal Lipoma: A Case Report and Review of Pathogenesis.
Cureus
August 2024
Clinical Sciences, California Northstate University College of Medicine, Elk Grove, USA.
Intradural spinal lipomas are rare benign lesions typically located in the lumbosacral region and associated with spinal dysraphism in children. When unassociated with spinal dysraphism, they are most often diagnosed in young children or adolescents following the emergence of neurological symptoms. In their most rare form, intradural spinal lipomas may be found in adults without spinal dysraphism.
View Article and Find Full Text PDFNondysraphic Intramedullary Spinal Cord Lipomas in the Adult Population.
World Neurosurg
October 2024
Department of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee, USA; Le Bonheur Neuroscience Institute, Le Bonheur Children's Hospital, Memphis, Tennessee, USA; Department of Neurosurgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA; Semmes-Murphey Clinic, Memphis, Tennessee, USA.
Objective: Intramedullary spinal cord lipomas without spinal dysraphism are rare. Although they are benign tumors, they can cause significant neurological deficits. Their tight adherence to the spinal cord presents a challenge for resection.
View Article and Find Full Text PDFNondysraphic intramedullary spinal cord lipoma: a case report.
Ann Med Surg (Lond)
June 2024
Department of Neurosurgery, Tribhuvan University Institute of Medicine, Maharajgunj, Nepal.
Introduction: Intramedullary nondysraphic spinal lipomas are extremely rare among primary spinal cord tumors. These patients present with nonspecific sensory symptoms followed by deterioration of motor symptoms. As the safety margins for neurological preservation are thin, meticulously locating the extent of the tumor and choosing the resection modalities is essential.
View Article and Find Full Text PDFNon-dysraphic intramedullary spinal cord lipoma of the child: Report of 3 cases.
Neurochirurgie
September 2023
Department of pediatric neurosurgery, University of Lille, Lille University Hospital, Lille, France.
Background And Purpose: Non-dysraphic intramedullary spinal cord lipomas (NDSCL) represent 1% of spinal cord tumors. They are less frequent than dysraphic spinal cord lipomas and clinical presentation is unspecific. There are no guidelines on surgical management.
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