| Literature DB >> 26439968 |
Divyanshu Dubey1, Anshudha Sawhney2, Benjamin Greenberg2, Andrea Lowden2, Worthy Warnack2, Pravin Khemani2, Olaf Stuve3, Steven Vernino2.
Abstract
Despite being a potentially reversible neurological condition, no clear guidelines for diagnosis or management of autoimmune encephalitis exist. In this study we analyzed clinical presentation, laboratory and imaging characteristics, and outcome of autoimmune encephalitis from three teaching hospitals. Non-paraneoplastic autoimmune encephalitis associated with antibodies against membrane antigens was the most common syndrome, especially in the pediatric population. Clinical outcome was better for patients with shorter latency from symptom onset to diagnosis and initiation of immunomodulation. Patients with underlying malignancy were less likely to respond well to immunomodulatory therapy. The clinical spectrum of autoimmune encephalitis is fairly broad, but prompt recognition and treatment often leads to excellent outcome.Entities:
Keywords: Autoimmune; Encephalitis; Limbic encephalitis; Paraneoplastic; Seizure
Mesh:
Year: 2015 PMID: 26439968 DOI: 10.1016/j.jneuroim.2015.08.014
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478