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Role of Diffusion MRI Tractography in Endoscopic Endonasal Skull Base Surgery
Published on: July 5, 2021
[Frontal meningioma en plaque: a rare presentation for a common tumor!]
J Bouguila1, R H Khonsari, K Ayashi
1Service d'ORL et de chirurgie maxillofaciale, CHU La-Rabta, 1007 Tunis, Tunisie. bouguila_jed@yahoo.fr
Introduction:
En plaque meningioma are a morphological subgroup of meningioma defined by a carpet or sheet-like lesion that infiltrates the dura and sometimes invades the bone. We present an exceptional case due to its localization and evolution.
Case:
A 41-year-old female patient consulted for progressive swelling of the left frontoparietal region. CT-scan revealed thickening of the cranial medulla, without cerebral lesion. The tumor was removed. Histological analysis confirmed en plaque meningioma which recurred 7 years after.
Discussion:
En plaque meningioma are a rare subtype of meningioma which rarely affects the skull vault. Relapse is frequent.
Insights
En plaque meningioma, a rare dural tumor, infiltrated the skull vault in an exceptional case. This rare meningioma subtype has a high risk of recurrence after surgical removal.
Area of Science:
- Neurosurgery
- Oncology
- Pathology
Background:
- En plaque meningioma is a rare subtype characterized by diffuse, sheet-like growth infiltrating the dura mater and potentially bone.
- This specific morphological subtype is uncommon, particularly when presenting as a lesion of the skull vault.
Observation:
- A 41-year-old female presented with progressive swelling in the left frontoparietal region.
- CT imaging revealed cranial bone thickening without intracranial mass effect.
- Surgical resection was performed, with histological confirmation of en plaque meningioma.
Findings:
- The en plaque meningioma recurred seven years after the initial surgical removal.
- This case highlights an unusual localization and disease progression for this meningioma subtype.
Implications:
- En plaque meningioma of the skull vault represents a rare clinical challenge.
- The high rate of recurrence underscores the need for vigilant long-term follow-up and potentially novel therapeutic strategies.
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