Meningioma. Variants:
meningothelial (WHO I)
fibrous (fibroblastic) (WHO I)
transitional (mixed) (WHO I)
psammomatous (WHO I)
angiomatous (WHO I)
microcystic (WHO I)
secretory (WHO I)
lymphoplasmacyte-rich (WHO I)
metaplastic (WHO I)
the following meningiomas exhibit more malignant behavior
clear cell (intracranial) (WHO II)
chordoid (WHO II)
atypical meningioma (WHO II)
papillary meningioma (WHO III)
rhabdoid meningioma (WHO III)
anaplastic (malignant) meningioma (WHO III)
mostly benign (1-2% anaplastic), slow-growing, extra-axial, circumscribed (non-infiltrative), arise from arachnoid membrane
often calcified, cause hyperostosis of adjacent bone
common locations: parasagittal convexity or falx (70%), sphenoid wing, tuberculum sellae,
foramen magnum, olfactory groove
Clinical Features
middle aged, slight female preponderance (M:F = 2:3), high progesterone receptors (increase in size with pregnancy), symptoms of increased ICP, focal deficits, usually solitary (10% multiple, likely with loss of NF2 gene/22q12 deletion)
Investigations
CT /w contrast: homogeneous, densely enhancing, along dural border ("dural tail"), well circumscribed
contrast enhanced MRI provides better detail
angiography
most are supplied by external carotid feeders (meningeal vessels)
also assesses venous sinus involvement, "tumour blush" commonly seen (prolonged contrast image)
octreotide scintigraphy: to establish if expression of somatostatin receptor
Treatment
conservative management for non-progressive, aSx lesions
surgery is treatment of choice if Sx or progression on sequential imaging (curative if complete resection)
SRS may be an option for lesions <3 cm
endovascular embolization to facilitate surgery
SRS or XRT for recurrent atypical/malignant meningiomas
Prognosis
>90% 5-yr survival, recurrence rate variable (often ~10-20%)
depends on extent of resection (Simpson's classification)
WHO Classification of Meningioma (by histology)
Grade 1: low risk of recurrence
Grade 2: intermediate risk of recurrence
Grade 3: high risk of recurrence