Tumefactive demyelination of the spinal cord: a case report
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu kazuistiky, časopisecké články, práce podpořená grantem
PubMed
26123208
DOI
10.1038/sc.2015.52
PII: sc201552
Knihovny.cz E-zdroje
- MeSH
- akvaporin 4 imunologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- magnetická rezonanční tomografie MeSH
- methylprednisolon terapeutické užití MeSH
- mícha patologie MeSH
- neuroprotektivní látky terapeutické užití MeSH
- oligoklonální proužky mozkomíšní mok MeSH
- poranění míchy mozkomíšní mok komplikace patologie terapie MeSH
- transverzální myelitida mozkomíšní mok komplikace patologie terapie MeSH
- výměna plazmy MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- práce podpořená grantem MeSH
- Názvy látek
- akvaporin 4 MeSH
- methylprednisolon MeSH
- neuroprotektivní látky MeSH
- oligoklonální proužky MeSH
STUDY DESIGN: Case report. OBJECTIVES: We report on a 52-year-old male patient with tumefactive demyelination of the spinal cord. SETTING: University Hospital and Jessenius Faculty of Medicine, Comenius University, Martin, Slovakia. BACKGROUND: In contrast to relatively frequent tumefactive fulminant lesions in the brain, cases affecting the spinal cord in isolation have been reported less frequently. METHODS: Description of the case report. RESULTS: Clinical, neuroradiological and necropsy findings are described in a 52-year-old man with tumefactive fulminant demyelination of the spinal cord. Progression of the demyelination process produced paraplegia, mild paresis of the right upper limb, neurogenic bladder and sensitive loss over 2 weeks. MRI scans revealed several ovoid lesions in cervical segments and tumefactive T2-hyperintense signals with oedema and post-contrast enhancement located in thoracic segments Th3 to Th6. Cerebrospinal fluid (CSF) examination displayed lymphomonocytic pleocytosis with normal proteinorhachia, positive CSF oligoclonal IgG bands (OCB) and elevated IgG index (1.55). Serum anti-AQP4-Ab was not tested. Stored frozen CSF samples were later repeatedly examined with negative findings of anti-AQP4-Ab. Treatment with high-dose methylprednisolon and plasma exchange had limited effect. Immunosuppressive medication was interrupted because of an acute urinary infection. The patient died suddenly because of pulmonary embolism as a secondary complication. Histopathology of the spinal cord confirmed active demyelination. We considered that tumefactive demyelination could be a variant of neuromyelitis optica. CONCLUSION: Our case could be anti-AQP4-Ab-negative longitudinally extensive transverse myelitis, a variant of neuromyelitis optica.
Clinic of Neurology Jessenius Faculty of Medicine in Martin Comenius University Martin Slovakia
Faculty of Medicine Palacky University in Olomouc Olomouc Czech Republic
Radiology Clinic Jessenius Faculty of Medicine in Martin Comenius University Martin Slovakia
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