
A study of 100 patients with spheno-orbital meningioma (SOM) revealed critical insights into its clinical, radiological, and pathological characteristics. The study population included 28 males and 72 females with an average age of 46.8 years. Proptosis was the most prevalent symptom, seen in 99% of cases. Radiologically, CT scans consistently showed hyperostosis with irregular edges, while MRI scans identified a dural tail sign in all patients. The tumors frequently infiltrated the temporal muscle, extraocular muscle, and lacrimal gland. Surgical intervention was performed in all cases, with 62 patients receiving postoperative radiotherapy. Grade I resections demonstrated the lowest recurrence rates, especially when combined with radiotherapy. Pathological examination indicated that intracranial tumors were softer and more prone to bleeding than intraorbital sections.
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