Intramedullary cavernous angiomas are rare vascular malformations; all published cases have been surgically approached posteriorly by standard laminectomy. We describe the case of a 63-year-old man with an intramedullary cavernous angioma, anteriorly located in the thoracic spinal cord. The angioma was operated on by transthoracic approach and totally removed.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1007/BF00831568 | DOI Listing |
Eur Spine J
December 2024
Department of Neurosurgery, Medical Research Institute KITANO HOSPITAL, PIIF Tazuke-Kofukai, Osaka, Japan.
Background: Complete removal of the lesion from the spinal cord cavernous malformation is crucial in patients with spinal cord cavernous malformation. Herein, we report that narrow-band imaging (NBI) is useful to confirm the complete removal of spinal cord cavernous malformations.
Clinical Presentation: A 45-year-old woman was followed up for the past seven years due to multiple intracranial cavernous malformations.
J Med Case Rep
November 2024
Department of Neurology, Taiyuan Central Hospital, Shanxi Medical University, No.5, Three Lanes East Road, Taiyuan, 030000, China.
Cureus
August 2024
Pediatric Neurology, Centre Hospitalier de Luxembourg, Luxembourg City, LUX.
We present a case of a 13-year-old boy with abdominal pain initially misdiagnosed as gastrointestinal in origin. Despite initial outpatient management, his symptoms rapidly deteriorated, revealing a central-medullary cavernous malformation causing spinal cord compression. This case underscores the importance of a comprehensive pediatric examination and highlights new treatment approaches for spinal cavernous malformations.
View Article and Find Full Text PDFRadiol Case Rep
November 2024
Interdisciplinary Department of Medicine, Section of Radiology and Radiation Oncology, University of Bari "Aldo Moro", Bari 70124, Italy.
Cavernous malformations are rare vascular anomalies of the central nervous system, occurring in the spinal cord in just 5% of cases. Despite being documented in the literature, intramedullary cavernous malformations are exceedingly rare and often challenging to distinguish from other intramedullary lesions. We report a case of a 42-year-old patient with back pain, right-sided dysesthesias, and impaired proprioception in the distal limbs for approximately 3 months.
View Article and Find Full Text PDFCureus
August 2024
Neurosurgery, Hospital de Braga, Braga, PRT.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!