Meningiomas of the Cerebellopontine Angle and Foramen Magnum

1994 ◽  
Vol 5 (2) ◽  
pp. 349-377 ◽  
Author(s):  
Albert L. Rhoton
2020 ◽  
Vol 11 ◽  
pp. 418
Author(s):  
Adedamola Adepoju ◽  
Ananth Narayan ◽  
Mahmoud Aldyab ◽  
David Foyt ◽  
Maria Peris-Celda

Background: Meningioma is one of the most common intracranial tumors with well-established radiologic features such as contrast enhancement, dural tail, and hyperostosis on computed tomography and magnetic resonance imaging. Contrast enhancement is usually homogeneous or heterogeneous based on tumor vascularity and underlying histopathology. Even in this context, faint or nonenhancing meningioma is exceedingly rare. Case Description: A 57-year-old male presented with progressive right hearing loss, disequilibrium, occasional difficulty swallowing, and facial numbness. Imaging demonstrated an extensive hypodense, nonenhancing right cerebellopontine angle mass extending from the interpeduncular, and ambient cisterns to the foramen magnum. The pathological analysis demonstrated a microcystic meningioma WHO Grade I. There are few reported case reports or series of minimal or nonenhancing meningiomas, and a systematic review was performed for these cases. Seven peer-reviewed articles with 14 verifiable cases were identified and reviewed for radiologic features, tumor location, and tumor classification. The majority of minimal or nonenhancing meningiomas were microcystic, and most of them located at the convexity. This is the second case reported of a nonenhancing meningioma at the cerebellopontine angle and petroclival region Conclusion: Meningioma should be considered a differential diagnosis for nonenhancing lesion at the cerebellopontine and petroclival regions.


2011 ◽  
Vol 69 (suppl_1) ◽  
pp. ons117-ons120 ◽  
Author(s):  
Tiffany R. Hodges ◽  
Isaac O. Karikari ◽  
Shahid M. Nimjee ◽  
June Tibaleka ◽  
Allan H. Friedman ◽  
...  

Abstract BACKGROUND AND IMPORTANCE: Calcifying pseudoneoplasms are rare tumors of the neuraxis. To our knowledge, this is only the second reported case in the literature of calcifying pseudoneoplasm of the cerebellopontine angle. The etiology and natural history of these neoplasms are not well understood. This case report provides a thorough review of the histology and potential origins of calcifying pseudoneoplasm. CLINICAL PRESENTATION: A 34-year-old previously healthy man presented with a 6-month history of progressive worsening headaches, fatigue, tinnitus, dizziness, and blurry vision. Neurological examination was notable for tongue deviation, tongue atrophy, and left uvula deviation. Computed tomography (CT) scanning showed a 3.3 × 3.5 cm densely calcified posterior fossa mass appearing to arise from the occipital bone. Magnetic resonance imaging (MRI) revealed a 4.3 × 2.9 × 2.9 cm left posterior fossa enhancing mass with the margin tip from the left occipital condyle. A transcondylar approach was used to resect the lesion. The mass was found to have eroded through the bone into the foramen magnum. Histopathological examination confirmed the diagnosis of calcifying pseudoneoplasm of the cerebellopontine angle. CONCLUSION: Calcifying pseudoneoplasms should be considered in the differential diagnosis of calcified cerebellopontine angle tumors. Histopathologic diagnosis is extremely important in the characterization of these lesions in order to direct the course of appropriate management. An inaccurate diagnosis of a malignant tumor can result in potentially harmful and unnecessary therapies, as prognosis for these lesions is generally favorable.


2013 ◽  
Vol 74 (S 01) ◽  
Author(s):  
John Leonetti ◽  
Nadieska Caballero ◽  
Jacob Ossoff ◽  
Sam Marzo ◽  
Douglas Anderson

2014 ◽  
Vol 75 (S 02) ◽  
Author(s):  
Beatriz Madero ◽  
P. Avan ◽  
A. Bazin ◽  
A. Chays ◽  
T. Mom ◽  
...  

2015 ◽  
Vol 76 (S 01) ◽  
Author(s):  
Paulo Mesqita Filho ◽  
Daniel Prevedello ◽  
Leo Ditzel Filho ◽  
Edward Kerr ◽  
Cristian Martinez ◽  
...  

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