| Literature DB >> 24192218 |
M Ringelstein1, I Metz2, K Ruprecht3, A Koch4, J Rappold5, J Ingwersen1, C Mathys6, S Jarius7, W Brück2, H-P Hartung1, F Paul8, O Aktas9.
Abstract
Longitudinally extensive transverse myelitis is characteristic but not pathognomonic for neuromyelitis optica spectrum disorders (NMOSDs) and may mimic local tumors. In this retrospective study based on a cohort of 175 NMOSD patients we identified seven patients who initially presented with a longitudinally extensive spinal cord lesion and underwent spinal cord biopsy due to magnetic resonance imaging (MRI)-suspected malignancies. Remarkably, routine neuropathology was inconclusive and did not guide the diagnostic process to anti-aquaporin-4 (AQP4)-seropositive NMOSD. Serious postoperative complications occurred in 5/7 patients and persisted during follow-up in 2/7 patients (29%). Considering these sequelae, AQP4-antibody testing should be mandatory in patients with inconclusive longitudinally extensive spinal cord lesions prior to biopsy.Entities:
Keywords: Spinal cord tumor; aquaporin-4 antibody; longitudinally extensive spinal cord lesion; longitudinally extensive transverse myelitis; neuromyelitis optica; spinal biopsy
Mesh:
Substances:
Year: 2013 PMID: 24192218 DOI: 10.1177/1352458513510981
Source DB: PubMed Journal: Mult Scler ISSN: 1352-4585 Impact factor: 6.312