Rhabdoid Meningioma-An Uncommon and Aggressive Variant
Asaranti Kar*, Gayatri Rath, Lity Mohanty, Pradip Behera, Sitaram Mohapatro, Anasuya Lenka and Shiva Soumendra Sahu
Department of Pathology, S.C.B.Medical College, Cuttack, Odisha, India
- *Corresponding Author:
- Asaranti Kar
Qrs. No.JO-1, S.C.B.Medical College Campus
Cuttack, Odisha-753007, India
E-mail: [email protected]
Received Date: July 29, 2013; Accepted Date: October 21, 2013; Published Date: October 23, 2013
Citation: Kar A, Rath G, Mohanty L, Behera P, Mohapatro S, et al. (2013) Rhabdoid Meningioma-An Uncommon and Aggressive Variant. J Cancer Sci Ther 5: 343-345. doi:10.4172/1948-5956.1000225
Copyright: © 2013 Kar A, et al. 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.
Rhabdoid meningioma is a rare subtype of meningiomas accounting for 1-3% of all intracranial meningiomas and classified as WHO Grade III tumor. It has an aggressive course and needs to be treated by both surgery and radiotherapy. Here we present a rare case of rhabdoid meningioma in a 24 year old lady with complaints of focal seizures, paresis and diplopia. CT & MRI showed a mass attached to dura in left posterosuperior frontoparietal region with peripheral edema. Histopathology showed large tumor cells arranged in sheets, whorls and papillary pattern. The patient was treated by surgery followed by radiation. This is reported to aware the surgical pathologists to keep this subtype as a differential diagnosis while interpreting any meningioma as it has an aggressive course.