Simple Summary Tumor-like lesions at the craniovertebral junction, including epidermoids,
dermoids, and neurenteric cysts present significant treatment challenges. Our review of …

Introduction Nerve sheath tumours arise from both the central and peripheral nervous
systems. In particular, cases of spinal or paraspinal origins are scarce and poorly covered in …

Key Clinical Message Craniovertebral junction (CVJ) schwannomas are rare tumors,
showing direct involvement of the atlanto‐occipital and atlanto‐axial joints. Microsurgical …

Schwannomatosis is a rare autosomal dominant hereditary syndrome disease characterized
by multiple schwannomas throughout the body, without bilateral vestibular schwannoma or …

Introduction: Schwannomas are benign solitary, slow-growing, encapsulated, asymptomatic
tumors arising from Schwann's sheath of nervous fibers. Objectives: The current paper …

Objective The goal of schwannoma resection is to control the tumor while preserving
neurological function. Schwannomas have a variable postoperative growth pattern …

Background Craniovertebral junction (CVJ) tumors are challenging due to their unique
anatomical location. This study aimed to evaluate the complexities in dealing with such …

Objectives We sought to perform a systematic review and meta-analysis of outcomes after
surgical resection of jugular foramen schwannomas (JFSs). Design A systematic review of …

Background/Objectives: The craniovertebral junction (CVJ) poses unique challenges in the
surgical management of intradural extramedullary (IDEM) tumors due to its complex …

Schwannomas overall account for approximately 8% of primary brain tumors, with the
majority of them arising from the vestibular nerves. 1, 2 Non-vestibular schwannomas are …