Literature DB >> 26220353

Autoimmune Encephalitis Following Bone Marrow Transplantation.

Geetanjali S Rathore1, Kathryn S Leung2, Eyal Muscal3.   

Abstract

BACKGROUND: Neurological complications, especially encephalopathy and seizures, are commonly seen in bone marrow transplant patients. Infections, chemotoxicity, graft versus host disease, or secondary central nervous system malignancies are the most common underlying etiologies. There is increased awareness that autoimmune encephalitis may cause neurological dysfunction in immunocompetent children. The potential role of such a mechanism in children undergoing bone marrow transplantation is unknown.
METHODS: We report a boy who developed autoimmune encephalitis with voltage-gated potassium channel-associated and thyroid autoantibodies subsequent to transplantation.
RESULTS: A 7-year-old boy presented with a change in behavior, poor attention, cognitive deficits, and abnormal movements 15 months after undergoing transplantation for idiopathic aplastic anemia. He had clinical and subclinical seizures and brain magnetic resonance imaging hyperintensities bilaterally in the uncal regions. His evaluation revealed high titers of voltage-gated potassium channel, leucine-rich glioma-inactivated 1 protein, and thyroglobulin antibodies suggestive of autoimmune limbic encephalitis. He showed significant improvement in behavior and neuropsychological testing and has remained seizure-free on levetiracetam after immunotherapy with corticosteroids and intravenous immunoglobulin.
CONCLUSION: Systemic autoimmune manifestations in bone marrow transplant patients have been well-documented, but autoimmune encephalitis after transplantation has yet to be described in children.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Hashimoto encephalopathy; autoimmune epilepsy; cognitive changes in bone marrow transplant patients; leucine-rich glioma-inactivated 1 protein (LGI1); limbic encephalitis; voltage-gated potassium channel (VGKC) associated antibody

Mesh:

Year:  2015        PMID: 26220353     DOI: 10.1016/j.pediatrneurol.2015.05.011

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  9 in total

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  9 in total

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