Metaplastic Meningioma Presenting with Anemia in A Young Boy Case Report and Review of the Literature

Ayesha Sajjad; Amna Shah Mehmood; Maria Tasneem Khattak; Naveed Zaman Akhunzada; Faryal Javaid; Sana Ullah Khan; Shifa Basharat; Ayesha Safdar1

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Publication Date: 2023/04/09

Abstract: Meningioma is the most common extra-axial, Dura-based tumor of the central nervous system. These tumors often present in middle to late adult life, especially in women, and account for 15% - 30% of all intracranial tumors(1). Incidence rate of 18.69 and 0.16 per 100,000 is recorded for patients above 40 years and 0-19 years age respectively(2). The World Health Organization (WHO) in its 2021 classification divides meningioma into Grade I (benign), Grade II (atypical), and Grade III (anaplastic) variants. It further subclassifies grade I meningioma into 9 subtypes: meningothelial, fibrous, transitional, psammomatous, angiomatous, microcystic, secretory, lymphoplasmacyte rich, and metaplastic(3). Metaplastic meningioma is the rarest subtype, and defined as a tumor containing focal or widespread mesenchymal components including osseous, cartilaginous, lipomatous, myxoid or xanthomatous tissue, singly or in combinations(4). We present a case of metaplastic meningioma with Myxoid, Xanthomatous and Osseous metaplasia presenting with anemia in a 17-year-old boy.

Keywords: Meningioma, Anemia, Immunohistochemistry

DOI: https://doi.org/10.5281/zenodo.7811122

PDF: https://ijirst.demo4.arinfotech.co/assets/upload/files/IJISRT23MAR2027.pdf

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