| Literature DB >> 36147770 |
Zachary A Kons1,2, Robert W Regenhardt1,3, Adam A Dmytriw1,4, Justin E Vranic1,4, Anh Huynh5, Matthew P Frosch5, Lawrence F Borges1, Aman B Patel1, Javier M Romero4, Christopher J Stapleton1.
Abstract
Spinal schwannomas are rare nerve root tumors that typically produce subtle symptoms from nerve root compression. These tumors are known to be heterogeneously hyperintense on T2-weighted MRI and avidly enhance with contrast. However, here we describe an L5 spinal schwannoma in a 66-year-old woman that was hypointense on T2-weighted imaging with other radiographic findings more closely aligning with a vascular lesion. The neuroradiologic characteristics on MRI, time resolved MR angiography, and catheter digital subtraction angiography are presented. The patient underwent a full workup for possible dural arteriovenous fistula and thrombosed venous varix before the nerve sheath tumor was discovered intraoperatively and confirmed as a schwannoma on histopathology.Entities:
Keywords: nerve compression syndromes; neurooncology; spinal cord diseases
Year: 2022 PMID: 36147770 PMCID: PMC9485699 DOI: 10.1177/19418744221112539
Source DB: PubMed Journal: Neurohospitalist ISSN: 1941-8744