Clinicopathological Study of Extra-Axial Small Round Cell Tumors of the Cranium

Conclusion: SRCTs are unusual tumors with a wide spectrum of histogenesis, biology and clinical presentation. Their rarity in cranium, atypical localization, overlapping clinical, and imaging features pose significant difficulty for clinicians, radiologists, and pathologists. A combined algorithmic analysis of the clinical, radiological, and histolopathological findings, supplemented with immunohistochemistry can aid in specific diagnosis which is crucial for optimal management.

Source: Neurology India - October 27, 2020 Category: Neurology Authors: BN Nandeesh Shilpa Rao Nishanth Sadashiva Anita Mahadevan TC Yasha Vani Santosh Source Type: research