98%
921
2 minutes
20
Background: Intradural osteoma is very rarely located in the subdural or subarachnoid space. Unfortunately, intradural osteoma lacks specificity in clinical manifestations and imaging features and there is currently no consensus on its diagnosis method or treatment strategy. Moreover, the pathogenesis of osteoma without skull structure involvement remains unclear.
Case Summary: We describe two cases of intradural osteomas located in the subdural and subarachnoid spaces, respectively. The first case involved a 47-year-old woman who presented with a 3-year history of intermittent headache and dizziness. Intraoperatively, a bony hard mass was found in the left frontal area, attached to the inner surface of the dura mater and compressing the underlying arachnoid membrane and brain. The second case involved a 56-year-old woman who had an intracranial high-density lesion isolated under the right greater wing of the sphenoid. Intraoperatively, an arachnoid-covered bony tumor was found in the sylvian fissure. The pathological diagnosis for both patients was osteoma.
Conclusion: Surgery and pathological examination are required for diagnosis of intradural osteomas, and craniotomy is a safe and effective treatment.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953386 | PMC |
http://dx.doi.org/10.12998/wjcc.v9.i8.1863 | DOI Listing |
J Clin Neurosci
June 2025
Department of Neurological Surgery, University of California, San Diego, CA, USA. Electronic address:
Introduction: At the time of its origination, endoscopic spine surgery (ESS) was introduced to advance minimally invasive spine surgical (MISS) techniques, aiming to reduce tissue traumatization and improve clinical outcomes. Initially, ESS was primarily applied to transforaminal diskectomies for treating low back pain and radiculopathy caused by lateral or posterolateral disc herniations. Early challenges included limited visualization, suboptimal camera systems, and restricted maneuverability of rigid endoscopes.
View Article and Find Full Text PDFClin Neurol Neurosurg
March 2022
Department of Neurosurgery, Ehime University School of Medicine, 454 Shitsukawa, Toon, Ehime 791-0295, Japan.
Surg Neurol Int
May 2021
Department of Neurosurgery, Punjab Institute of Neurosciences, Lahore General Hospital, Lahore, Punjab, Pakistan.
Background: Paranasal sinus osteoma in association with intracranial mucocele is a rare entity while intradural extension is even rarer. Our aim of presenting this case is to highlight the diagnostic pitfalls and reiterate the importance of prompt treatment of expected complications.
Case Description: A 35-year-old known epileptic, for the past 5 years, presented with altered sensorium for the past 2 days.
World J Clin Cases
March 2021
Department of Neurosurgery, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou 310009, Zhejiang Province, China.
Background: Intradural osteoma is very rarely located in the subdural or subarachnoid space. Unfortunately, intradural osteoma lacks specificity in clinical manifestations and imaging features and there is currently no consensus on its diagnosis method or treatment strategy. Moreover, the pathogenesis of osteoma without skull structure involvement remains unclear.
View Article and Find Full Text PDFNo Shinkei Geka
August 2020
Department of Neurosurgery, Japan Organization of Occupational Health and Safety, Osaka Rosai Hospital.
The formation of symptomatic intradural mucocele associated with a paranasal osteoma is rare, and no standard treatment has been established. Here, we present a case of intradural mucocele in a 27-year-old man complaining of headache and generalized convulsion. Cranial CT and brain MRI showed a left frontoethmoidal osteoma extending into the left anterior cranial fossa and orbit along with a mass in the left frontal lobe.
View Article and Find Full Text PDF