A 31-year-old female with lymphoblastic lymphoma developed myasthenia gravi
s (MG) 26 months after receiving an allogeneic bone marrow transplant (BMT)
from an HLA-identical sister. She presented with classic symptoms and elec
tromyographic evidence of the disorder approximately 2 weeks after electing
to abruptly discontinue her immunosuppressive medications. She initially r
esponded to steroids and acetylcholinesterase inhibitors. Her subsequent co
urse has been characterized by episodes of moderately severe weakness that
respond to intravenous immunoglobulin and prednisone, This case of post-tra
nsplant MG is only the second reported to have occurred in association with
BMT for lymphoblastic lymphoma. Potential risk factors for the development
of post-transplant MG are discussed including underlying hematological dis
order, HLA phenotype, family history of MG, the presence of chronic GVHD, a
nd recent cessation of immune suppression.