


The etiology of anterior temporal lobe perivascular spaces remains uncertain but is likely related to vascular compression of small communicating channels by a looped MCA branch, resulting in focal CSF accumulation and abnormal local CSF dynamics.
Unlike typical perivascular (Virchow-Robin) spaces elsewhere in the brain, anterior temporal lobe variants frequently have associated T2/FLAIR hyperintense edema (~80% of cases), which ranges from mild to extensive and can evolve over time.
The presence of surrounding edema can create a concerning appearance mimicking a cystic tumor with surrounding vasogenic edema, leading to unnecessary workup, biopsy, and potential over-treatment if the entity is not recognized.
If histology is obtained, reactive astrocytosis surrounding the cyst (normal brain response to the lesion) can be misinterpreted as a minimally hypercellular astrocytic tumor; IDH wild-type status confirms these are normal cells, not neoplastic.
Recognition of this entity is critical to avoid unnecessary surgical intervention, additional treatment, and patient morbidity through informed conservative follow-up imaging.
High-resolution T2-weighted sequences, post-contrast T1-weighted imaging, and MRA are essential for diagnosis and demonstrating the key distinguishing features (vascular loop, no enhancement, cortical thinning).
Describe as: "CSF-signal lesion in [anterior temporal lobe/frontal operculum] with associated T2/FLAIR hyperintense edema and focal cortical thinning at the site of adjacent MCA loop indentation; no enhancement; imaging features consistent with opercular perivascular space rather than neoplasm. Recommend follow-up to confirm stability."