| Literature DB >> 3526178 |
G B Bolger, K M Sullivan, A M Spence, F R Appelbaum, R Johnston, J E Sanders, H J Deeg, R P Witherspoon, K C Doney, J Nims.
Abstract
Three patients with chronic graft-versus-host disease (GVHD) developed myasthenia gravis (MG) 762 to 1,180 days after allogeneic bone marrow transplantation. Symptoms of MG were observed after taper or discontinuation of immunosuppressive treatment of chronic GVHD. All patients developed antibodies to acetylcholine receptor, and one had antibody formation to striated muscle. One patient died of complications of treatment of MG. The severity of disease underscores the importance of the differential diagnosis and the need for prompt therapy of this late complication after human bone marrow transplantation.Entities:
Mesh:
Substances:
Year: 1986 PMID: 3526178 DOI: 10.1212/wnl.36.8.1087
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910