Meckel cave tumors are usually asymptomatic and can be followed if characteristically benign findings are seen on MRI or CT. Differential considerations for masses in the Meckel cave include:
- Trigeminal schwannoma: The case shown above. Relatively rare. Can be seen with neurofibromatosis type 2 or as an isolated entity. Smooth margins, usually low on T1 and high on T2. Avid enhancement with or without cystic components.
- Epidermoid tumor: Arise from incomplete cleavage of neural ectoderm from cutaneous ectoderm and grow by desquamation of epithelial cells. Lobulated margins, Low on T1 and high on T2, minimal mass effect.
- Meningioma: Isointense to surrounding normal brain parenchyma on T1- and T2-weighted images. May calcify.
- Trigeminal lipoma: Rare. Looks like fat. Infiltrates the trigeminal nerve fascicles.
- Primary lymphoma: Can mimic trigeminal schwannoma. Consider this diagnosis in immunocompromised patients. The presence of an apparent dural tail can suggest lymphoma in the absence of hyperostosis (typically seen with meningiomas).
- Arachnoid cyst: Fluid signal on all sequences.
- Chordoma: Arises from adjacent clivus.
References
- Abdel Aziz KM, van Loveren HR. Primary lymphoma of Meckel's cave mimicking trigeminal schwannoma: case report. Neurosurgery. 1999 Apr;44(4):859-62; discussion 862-3.
- Beck DW, Menezes AH. Lesions in Meckel's cave: variable presentation and pathology. J Neurosurg. 1987 Nov;67(5):684-9.
- Yuh WT, Wright DC, Barloon TJ, Schultz DH, Sato Y, Cervantes CA. MR imaging of primary tumors of trigeminal nerve and Meckel's cave. AJR Am J Roentgenol. 1988 Sep;151(3):577-82.
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