Meningiomas are the most common primary brain tumors, accounting for approximately 39% of all central nervous system tumors. The average annual age-adjusted incidence rate for all malignant and non-malignant brain tumors is reported at 24.83 per 100,000 population, with malignant tumors at 6.94 and non-malignant at 17.88. In pediatric populations (ages 0-19), the incidence rate is notably lower at 6.13 per 100,000. Survival rates vary significantly between malignant and non-malignant cases, with a five-year relative survival rate of 35.7% for malignant tumors and 91.8% for non-malignant tumors (ref: Ostrom doi.org/10.1093/neuonc/). Recent studies have identified genetic and molecular factors contributing to meningioma development, including the activation of Hedgehog signaling in 6.5% of cases, often linked to mutations in pathway mediators like SMO. Notably, 35.6% of meningiomas without known drivers exhibit structural variations on chromosomes 2q35 and 7q36.3, indicating a complex genetic landscape (ref: Youngblood doi.org/10.1038/s41467-023-41926-y/). Furthermore, a multicenter cohort study on grade 3 meningiomas has provided insights into survival and recurrence outcomes, emphasizing the need for more comprehensive data on this rare subtype (ref: Tosefsky doi.org/10.3171/2023.6.JNS23465/).