Fulminant Devic disease successfully treated by lymphocytapheresis
- 18 May 2006
- journal article
- Published by BMJ in Journal of Neurology, Neurosurgery & Psychiatry
- Vol. 77 (9) , 1094-1095
- https://doi.org/10.1136/jnnp.2005.086306
Abstract
In August 2001, a 27-year-old woman developed acute loss of vision and sensory disturbance in both lower extremities after coughing. The next morning (day 2), she was totally blind and was admitted to our hospital. Neurological examination showed total blindness, papilloedema, moderate muscle weakness of the hip and thigh muscles, positive pathological reflexes of the limbs, hyper-reflexia and sensory loss below the T4–5 level. Loss of vesicorectal function and perspiration below the chest were also observed.Keywords
This publication has 5 references indexed in Scilit:
- Activation of humoral immunity and eosinophils in neuromyelitis opticaNeurology, 2004
- A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosisPublished by Elsevier ,2004
- Tc1/Tc2 and Th1/Th2 balance in Asian and Western types of multiple sclerosis, HTLV-I-associated myelopathy/tropical spastic paraparesis and hyperIgEaemic myelitisJournal of Neuroimmunology, 2001
- Lymphocytaplasmapheresis in Devic's syndromeTransfusion, 1985
- Use of lymphoplasmapheresis or plasmapheresis in the management of acute renal allograft rejectionJournal of Clinical Apheresis, 1982