We've updated our Privacy Policy to make it clearer how we use your personal data.
We use cookies to provide you with a better experience, read our Cookie Policy
EP29213
Abstract: The 28-year-old female, from Brasília, Brazil, presented in April, 2018 to the Section of Neurology at Brasília Air Force Hospital (HFAB) with no pathological history, came to the complaint with amaurosis on the sudden left that evolved from partial to total in 48 hours and persistent headache. Complaint for more than one year of paraesthesia of the upper limbs without considering that fact to seek medical assistance. After investigation including nuclear magnetic resonance (MRI) of the brain and spinal cord and laboratory findings, the positive test for anti-immunoglobulin G antibodies (AQP4-IgG).
In the cervical MRI, demonstrated T2-hyperintense (Figure-1E) demyelinating areas extending from C2 to C5. The cranial MRI examination describes T2-hyperintense with increased post Gadolinium T1 at the left optic nerve. The patient was diagnosed with NMO according to the diagnostic criteria which were revised in 2006 and 2015, and 1 gr / day IV methylprednisolone was administered for 7 days
Remain in follow-up service. Summary: Neuromyelitis optica (NMO), also known as Devic’s disease, is a serious, idiopathic and inflammatory demyelinating syndrome of the central nervous system (CNS). This devastating disease is classically characterized by selective and severe attacks of the optic nerve and spinal cord with or without recovery, and is potentially fatal. Key words: Neuromyelitis optica; aquaporin-4-IgG antibody, MRI. References: 1. Argyriou AA, Makris NN. Neuromyelitis optica: a distinct demyelinating disease of the central nervus system. Acta Neurol Scand 2008; 118: 209-17.
2. Sellner J, Boggild M, Clanet M, Hintzen RQ, Illes Z, Montalban X, et al. EFNS guidelines on diagnosis and management of neuromyelitis. Eur J Neurol 2010; 17: 1019-32.
3. Pittock SJ, Lennon VA, Krecke K, Wingerchuk DM, Lucchinetti CF and Weinshenker BG. Brain abnormalities in optic neuromyelitis. Arch Neurol 2006; 63: 390-396.
4. Kim W, MS Park, Lee SH and others. Characteristic abnormalities of brain magnetic resonance in the central nervous system aquaporin- autoimmunity. Mult Scler 2010; 16: 1229-1236.
5. Bichuetti DB, Rivero RL, Oliveira DM, et al. Optic neuromyelitis: cerebral abnormalities in a Brazilian cohort. 2008; 66: 1-4.
6. Saikali P, Cayrol R, Vincent T. Anti-aquaporin-4 autoantibodies orchestrate the pathogenesis in neuromyelitis optica.
In the cervical MRI, demonstrated T2-hyperintense (Figure-1E) demyelinating areas extending from C2 to C5. The cranial MRI examination describes T2-hyperintense with increased post Gadolinium T1 at the left optic nerve. The patient was diagnosed with NMO according to the diagnostic criteria which were revised in 2006 and 2015, and 1 gr / day IV methylprednisolone was administered for 7 days
Remain in follow-up service. Summary: Neuromyelitis optica (NMO), also known as Devic’s disease, is a serious, idiopathic and inflammatory demyelinating syndrome of the central nervous system (CNS). This devastating disease is classically characterized by selective and severe attacks of the optic nerve and spinal cord with or without recovery, and is potentially fatal. Key words: Neuromyelitis optica; aquaporin-4-IgG antibody, MRI. References: 1. Argyriou AA, Makris NN. Neuromyelitis optica: a distinct demyelinating disease of the central nervus system. Acta Neurol Scand 2008; 118: 209-17.
2. Sellner J, Boggild M, Clanet M, Hintzen RQ, Illes Z, Montalban X, et al. EFNS guidelines on diagnosis and management of neuromyelitis. Eur J Neurol 2010; 17: 1019-32.
3. Pittock SJ, Lennon VA, Krecke K, Wingerchuk DM, Lucchinetti CF and Weinshenker BG. Brain abnormalities in optic neuromyelitis. Arch Neurol 2006; 63: 390-396.
4. Kim W, MS Park, Lee SH and others. Characteristic abnormalities of brain magnetic resonance in the central nervous system aquaporin- autoimmunity. Mult Scler 2010; 16: 1229-1236.
5. Bichuetti DB, Rivero RL, Oliveira DM, et al. Optic neuromyelitis: cerebral abnormalities in a Brazilian cohort. 2008; 66: 1-4.
6. Saikali P, Cayrol R, Vincent T. Anti-aquaporin-4 autoantibodies orchestrate the pathogenesis in neuromyelitis optica.
Ask the author a question about this poster.
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
Related Posters
CERVICAL FIBROID PARODYING AS VAGINAL PROLAPSE
DR GEETANJALI KRISHNAN, DR SATHYA BALASUBRAMANIAM
Developing a robust Quantitative Systems Pharmacology model of adeno-associated virus (AAV) based gene therapy for clinical applications
Satyajit Rao, Jatin Narula, Zhiwei Zhang, Haobin Luo, Glen Ko, Cynthia J Musante, Nessy Tania
ISTHMOCELE A RECAP
DR RAJASRI,DR GEETANJALI
Method of obtaining highly effective stable, bioactive nanosized silver hydrosol with less toxicity for use in medicine and nano-oncology
Vram Khachatryan
Quantitative systems pharmacology model of the effect of tau hyperphosphorylation on synaptic plasticity
Stepan Lerner, Tatiana Karelina
