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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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April 23, 2020
  • Description
  • Legends
  • Legends 2
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  • Companion Case
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Mesencephalic Exophytic Cavernous Malformation

  • Background:
    • Cavernous malformations are occult lesions on catheter angiograms (formerly known as cryptogenic vascular lesions). The estimated incidence is approximately 0.5% (0.4–0.6%). The prevalence in the brain stem varies from 8.5% to 35%. They may be single or multiple, familial or sporadic (80%), and congenital or de novo.
    • The most common location in the brain stem is the pons (62%), followed by the midbrain (14%), pontomesencephalic and pontomedullary junction (12%), and medulla (5%).
  • Clinical Presentation:
    • It varies from headaches to neurologic deficits depending on the extent of hemorrhage and destruction of brain parenchyma.
  • Key Diagnostic Features:
    • Typically have lobulated appearance with signal dephasing on T2* sequences and commonly internal septa
    • Atypical lesions can be exophytic or even within the cistern (only few reports, with no actual percent available in the literature).
    • A complete T2-hypointense rim may be absent and no associated siderosis in the adjacent parenchyma seen.
    • Atypical locations are usually in small case series or case reports, so the real prevalence and incidence are hard to establish.
  • Differential Diagnoses:
    • Epidermoid cyst: It follows CSF signals and shows diffusion restriction.
    • White epidermoid cyst: Has high protein content and shows high signal intensity on T1-weighted images and low signal intensity on T2-weighted images
    • Meningioma: Shows intense enhancement
    • Melanotic schwannoma: Shows some cystic component and enhancing components
  • Treatment:
    • Surgical resection is often risky with brain stem lesions, though proper surgical corridors are well established.
    • Radiosurgery may be an option, with various degrees of success in the published series.

Suggested Reading

  1. Bertalanffy H, Gilsbach JM, Eggert HR, et al. Microsurgery of deep-seated cavernous angiomas: report of 26 cases. Acta Neurochir (Wien) 1991;108:91–99
  2. Bruneau M, Bijlenga P, Reverdin A, et al. Early surgery for brainstem cavernomas. Acta Neurochir (Wien) 2006;148:405–14
  3. Rajagopal N, Kawase T, Mohammad AA, et al. Timing of surgery and surgical strategies in symptomatic brainstem cavernomas: review of the literature. Asian J Neurosurg 2019;14:15–27
  4. Fritschi JA, Reulen H-J, Spetzler RF, et al. Cavernous malformations of the brain stem. Acta Neurochirurgica 1994;130:35–46

Current Issue

American Journal of Neuroradiology: 46 (6)
American Journal of Neuroradiology
Vol. 46, Issue 6
1 Jun 2025
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