| Literature DB >> 31525619 |
Roberta Di Giacomo1, Francesco Deleo2, Chiara Pastori3, Giuseppe Didato4, Francesca Andreetta5, Angelo Del Sole6, Marco de Curtis7, Flavio Villani8.
Abstract
We report the case of a 42-year-old woman who presented with vertigo and migraine and rapidly developed cognitive decline and seizures. Both serum and cerebro-spinal fluid samples showed high titer of anti-glutamic acid decarboxylase (anti-GAD65) antibodies (998,881 IU/ml and 54,687 IU/ml respectively). Limbic encephalitis was diagnosed and high dose steroids treatment started. During one-year follow-up, without further immunomodulatory therapy, the patient became seizure free, and cognitive functions returned to normal. Serum anti-GAD65 antibodies titer decreased significantly but remained elevated (192,680 IU/ml). We discuss the prognostic and pathogenic value of high titer anti-GAD65 antibodies and its variations in a case of autoimmune limbic encephalitis.Entities:
Keywords: Anti-glutamic acid decarboxylase 65 antibody; Autoimmune encephalitis; Immunotherapy; Limbic encephalitis; Neuroimmunology
Year: 2019 PMID: 31525619 DOI: 10.1016/j.jneuroim.2019.577063
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478