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AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

Case of the Week

Section Editors: Matylda Machnowska1 and Anvita Pauranik2
1University of Toronto, Toronto, Ontario, Canada
2BC Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada

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Submit a Case Previous Cases ASPNR Pediatric Cases

October 22, 2012
  • Description
  • Legends
  • Diagnosis
  • Brain Teaser
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Spinal Epidural Angiolipoma

  • Angiolipomas are benign soft tissue-vascular tumors, rarely seen in the CNS. When seen, they are mostly located in the posterior epidural space of the thoracic spinal canal, and account for 0.14% of all spinal axis tumors.
  • They are composed of normal adipose tissue and blood vessels, likely arising from pluripotent mesenchymal stem cells.
  • Clinical presentation: acute or sub-acute motor, sensory, and autonomic disturbances.
  • Key Diagnostic Features: Multisegmental, often posterior, spinal epidural mass, predominantly hypodense on CT, hyperintense on T2WI and T1WI, with hypointense foci on T1WI and intense contrast enhancement. May extend through neural foramina into paravertebral soft tissues. Rarely, bone invasion can be seen.
  • DDx: hemangioma, schwannoma, meningioma, metastasis, lymphoma
  • Rx: surgical excision

Suggested Reading

Gelabert-González M, García-Allut A. Spinal extradural angiolipoma: report of two cases and review of the literature. Eur Spine J2009;18:324-35. doi: 10.1007/s00586-008-0858-8

Provenzale JM, McLendon RE. Spinal angiolipomas: MR features. AJNR Am J Neuroradiol 1996;17:713-9.

Current Issue

American Journal of Neuroradiology: 46 (6)
American Journal of Neuroradiology
Vol. 46, Issue 6
1 Jun 2025
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Print ISSN: 0195-6108 Online ISSN: 1936-959X

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