Well, I take back the cystic part (I mixed up the T2 with the contrast sequence) but this is a simple meningioma. While its true that meningiomas have estrogen receptors, the biggest giveaway is the smooth non-infiltrating margins and the dural attachment. Hyperostosis of the overlying bone can occur as well.
Here's a quick algorithm off the top of my head (I only know this because I love neurosurgery and wrote a couple of papers on this but that was some time ago and so you may have to verify some of this):
Intra-axial (within parenchyma) supratentorial: glial tumors: GBMs (short history, older patients, can bleed postop), oligodendrogliomas etc. Pineal region neoplasms are frequently germ cell tumors.
Intra-axial infratentorial: Mets (unless proven otherwise in adults). Pilocytic astrocytomas or medulloblastomas (drop mets in cord) in kids: cerebellar mass +/- hydrocephalus. Hemangioblastomas if VHL-ish history or high hematocrit.
Extra-axial (outside parenchyma): meningiomas (often convexity, can be elsewhere; look for dural attachment or dural tail - enhancement along the dura beyond the attachment of the tumor. Schwannomas: trigeminal in the middle cranial fossa (Meckel's cave), vestibular in CP angle.
Extra-axial: midline sellar-suprasellar: Pituitary adenomas or craniopharyngiomas (cystic/calcified on CT). Similar presentation but cranios more often in kids. Rarely optic pathway gliomas in NF1 or tuberculum sellae meningiomas.
Extra-axial intraventricular: ependymomas (Tuberous sclerosis)/meningiomas/central neurocytomas (RARE!)
Hope this helps. I don't have time to cross-check this as Step 1 is in three days' time for me, but let me know if there are any mistakes!