| Literature DB >> 29455369 |
Malte Ottenhausen1, Georgios Ntoulias1, Imithri Bodhinayake2, Finn-Hannes Ruppert1, Stefan Schreiber1, Annette Förschler3, John A Boockvar4, Andreas Jödicke5.
Abstract
Among spinal tumors that occur intradurally, meningiomas, nerve sheath tumors, ependymomas, and astrocytomas are the most common. While a spinal MRI is the state of the art to diagnose intradural spinal tumors, in some cases CT scans, angiography, CSF analyses, and neurophysiological examination can be valuable. The management of these lesions depends not only on the histopathological diagnosis but also on the clinical presentation and the anatomical location, allowing either radical resection as with most extramedullary lesions or less invasive strategies as with intramedullary lesions. Although intramedullary lesions are rare and sometimes difficult to manage, well-planned treatment can achieve excellent outcome without treatment-related deficits. Technical advances in imaging, neuromonitoring, minimally invasive approaches, and radiotherapy have improved the outcome of intradural spinal tumors. However, the outcome in malignant intramedullary tumors remains poor. While surgery is the mainstay treatment for many of these lesions, radiation and chemotherapy are of growing importance in recurrent and multilocular disease. We reviewed the literature on this topic to provide an overview of spinal cord tumors, treatment strategies, and outcomes. Typical cases of extra- and intramedullary tumors are presented to illustrate management options and outcomes.Entities:
Keywords: Astrocytoma; Dumbbell tumor; Ependymoma; Intradural; Intramedullary; Meningioma; Neurofibroma; Schwannoma; Spinal
Mesh:
Year: 2018 PMID: 29455369 DOI: 10.1007/s10143-018-0957-x
Source DB: PubMed Journal: Neurosurg Rev ISSN: 0344-5607 Impact factor: 3.042