AI Article Synopsis

  • The review focuses on the latest trends in treating non-vestibular cranial nerve schwannomas, which are rare tumors making up 5-10% of such cases.
  • Treatment plans should be personalized based on the tumor's size, location, and any functional issues they may cause.
  • Sometimes, surgical removal is not fully possible due to the tumor's position, leading to alternatives like radiosurgery or monitoring small tumors over time rather than immediate intervention.

Article Abstract

The aim of this review is to analyze the latest trends in the management of non-vestibular skull base and intracranial schwannomas in order to optimize tumor control and quality of life. Non-vestibular cranial nerve schwannomas are rare lesions, representing 5-10% of cranial nerve schwannomas. Management decisions should be individualized depending on tumor size, location and associated functional deficits. Generally, large sized schwannomas exerting significant mass effect with increased intracranial pressure are treated surgically. In some cases, even after optimal skull base resection, it is not possible to achieve a gross total resection because tumor location and extent and/or to reduce morbidity. Thus, subtotal resection followed by stereotactic radiosurgery or fractioned radiotherapy offers an alternative approach. In certain cases, stereotactic radiosurgery or radiotherapy alone achieves good tumor control rates and less morbidity to gross total resection. Finally, given the slow growth rate of most of these tumors, observation with periodic radiographic follow-up approach is also a reasonable alternative for small tumors with few, if any, symptoms.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822088PMC
http://dx.doi.org/10.2147/CMAR.S287410DOI Listing

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