| Literature DB >> 35689724 |
Carlos Suárez1, Fernando López2,3, Juan P Rodrigo4,5, William M Mendenhall6, Remco de Bree7, Antti A Mäkitie8, Vincent Vander Poorten9,10, Robert P Takes11, Stefano Bondi12, Luiz P Kowalski13, Ashok R Shaha14, Veronica Fernández-Alvarez15, Julio C Gutiérrez16, Nina Zidar17, Carlos Chiesa-Estomba18, Primoz Strojan19, Alvaro Sanabria20,21, Alessandra Rinaldo22, Alfio Ferlito23.
Abstract
Benign peripheral non-cranial nerve sheath tumors are rare lesions, including both schwannomas and neurofibromas. These tumors arise from Schwann cells, and may originate from any peripheral, cranial, or autonomic nerve. Most of them are localized and sporadic but multifocal systemic forms can occur. Cervical sympathetic chain, brachial plexus, cervical plexus and spinal roots and nerves are the major nerve systems commonly affected. Dumbbell-shaped intra- and extradural tumors occur most commonly in the cervical spine, as well as purely extradural and paravertebral tumors. The management of these tumors has improved greatly owing to the developments in imaging techniques and surgical innovations such as endoscopically assisted approaches and robotic surgery. Microsurgical intracapsular excision of the tumor helped by the use of intraoperative fluorescent dyes and intraoperative neurophysiological monitoring minimize postoperative neural deficit, since most schwannomas are encapsulated. Most tumors can be removed with a low rate of complications and recurrence. Radiotherapy should be considered for growing lesions that are not amenable to surgery. In asymptomatic patients, observation and serial scans is an option for elderly infirm patients.Entities:
Keywords: Brachial plexus; Neurofibroma; Non-cranial nerves; Schwannoma; Spinal nerves; Sympathetic chain
Mesh:
Year: 2022 PMID: 35689724 DOI: 10.1007/s12325-022-02191-5
Source DB: PubMed Journal: Adv Ther ISSN: 0741-238X Impact factor: 4.070