- Department of Neurosurgery, PGIMER, Chandigarh, India
- Department of Radiodiagnosis, PGIMER, Chandigarh, India
- Department of Histopathology, PGIMER, Chandigarh, India
Correspondence Address:
Pravin Salunke
Department of Histopathology, PGIMER, Chandigarh, India
DOI:10.4103/2152-7806.99940
Copyright: © 2012 Salunke P. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.How to cite this article: Salunke P, Pal BK, Vyas S, Radotra BD. Clear cell meningioma masquerading as trigeminal schwannoma. Surg Neurol Int 21-Aug-2012;3:93
How to cite this URL: Salunke P, Pal BK, Vyas S, Radotra BD. Clear cell meningioma masquerading as trigeminal schwannoma. Surg Neurol Int 21-Aug-2012;3:93. Available from: http://sni.wpengine.com/surgicalint_articles/clear-cell-meningioma-masquerading-as-trigeminal-schwannoma/
Sir,
Clear cell meningioma (CCM) is a rare variant of meningioma with an aggressive clinical course and usually occurs in the cerebello pontine angle (CPA) or cauda equina.[
A 14-year-old female presented with left-sided facial numbness and heaviness for 2.5 months, followed by left-sided hearing loss and features of raised intracranial pressure for 2 months. A month later she developed left facial paresis of lower motor neuron type along with difficulty in swallowing and imbalance while walking with right lower limb weakness. Clinical examination revealed bilateral papilledema with left-sided trigeminal (both sensory and motor), facial (LMN type) involvement. The left glossopharyngeal, vagus, and hypoglossal nerves were involved. She had left-sided cerebellar signs with subtle right hemiparesis. Contrast-enhanced CT [
She underwent a subtotal excision of the tumor through the left retromastoid approach. The lesion was grayish in color and was relatively firm and less suckable. However, CUSA was helpful. The capsule of the lesion was left. There was injury to the superior petrosal sinus and the patient succumbed to venous infarction a week later. Unfortunately, autopsy was not performed.
Histopathological examination showed round to polygonal cells arranged in whorls, showing clear cytoplasm and round to oval nuclei with dispersed chromatin and insconspicuous nucleoli. There was perivascular and interstitial deposition of collagenous material in a block manner. Tumor cells tested positive for PAS and epithelial membrane antigen [
Trigeminal schwannoma typically grows from posterior fossa into the middle cranial fossa as the lesion grows along the nerve fibers. The truncation of petrous apex suggests chronic compression and is usually seen with trigeminal schwannoma. Occasionally lymphoma or lymphohistiocytic inflammation may spread along the nerve fibers to occupy both the posterior and the middle cranial fossa thereby, mimicking a schwannoma.[
Clear cell meningioma is a rare variant that is often seen in the CPA and is seen in relatively younger patients. The behavior of this variant is aggressive and is included in Grade II WHO.[
Our patient had rapidly worsening symptoms over 2 months and was relatively young. The clinical features suggested an aggressive lesion rather than a schwannoma. However, the radiology showed a lesion straddling across the petrous to occupy both the middle cranial fossa and posterior fossa along with truncation of petrous suggesting a trigeminal schwannoma.
The above case highlights the potential of meningiomas to grow along the nerve fibers straddling across the petrous to occupy both middle cranial and posterior fossa along with erosion of petrous mimicking a trigeminal schwannoma. Whether, such a phenomenon is limited to more aggressive meningiomas like clear cell variant remains unclear.
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