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Title

Spinal ependymoma in adults: a multicenter investigation of surgical outcome and progression-free survival
Authors
Wostrack, Maria
Ringel, Florian
Eicker, Sven O.
Jaegersberg, Max
Schaller, Karl Lothard
Kerschbaumer, Johannes
Thomé, Claudius
Shiban, Ehab
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Published in Journal of Neurosurgery: Spine. 2018, vol. 28, no. 6, p. 654-662
Abstract Spinal ependymomas are rare glial neoplasms. Because their incidence is low, only a few larger studies have investigated this condition. There are no clear data concerning prognosis and therapy. The aim of the study was to describe the natural history, perioperative clinical course, and local tumor control of adult patients with spinal ependymomas who were surgically treated under modern treatment standards.
Keywords Ependymoma — Neoplasms — Spinal cord — Recurrence — Local — Spinal intradural tumor — Oncology
Identifiers
PMID: 29521579
Full text
Article (Published version) (3.2 MB) - document accessible for UNIGE members only Limited access to UNIGE
Other version: https://thejns.org/view/journals/j-neurosurg-spine/28/6/article-p654.xml
Structures
Faculté de médecine / Section de médecine clinique / Département des neurosciences cliniques
Research group Groupe Schaller Karl Lothard (neurochirurgie) (851)
Citation
(ISO format) 		WOSTRACK, Maria et al. Spinal ependymoma in adults: a multicenter investigation of surgical outcome and progression-free survival. In: Journal of Neurosurgery: Spine, 2018, vol. 28, n° 6, p. 654-662. doi: 10.3171/2017.9.SPINE17494 https://archive-ouverte.unige.ch/unige:126300

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Deposited on : 2019-11-14

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