| Literature DB >> 32371280 |
Roberta Di Giacomo1, Davide Rossi Sebastiano2, Daniele Cazzato2, Francesca Andreetta3, Paolo Pozzi4, Silvia Cenciarelli5, Francesco Deleo6, Chiara Pastori6, Giuseppe Didato6, Marco de Curtis6, Flavio Villani7.
Abstract
We report the case of a 68-year-old man who presented with ataxia, insomnia, rapidly developing cognitive decline, seizures and small vessel vasculitis. Both serum and cerebro-spinal fluid samples showed positive titre of anti-CASPR2 antibodies. Limbic encephalitis was diagnosed and immunomodulatory therapy was started with benefit. After one-year follow-up, the patient relapsed with a difficult-to-treat respiratory failure, brainstem involvement, neuropathic pain and severe dysautonomia with esophageal dysfunction. We discuss here the occurrence of life-threating complication such as respiratory dysfunction in CASPR2 limbic encephalitis. Furthermore, we showed different phenotype and treatment response during disease onset compared to relapse. This case expands the clinical spectrum of anti-CASPR2 associated disease, underlying the need for respiratory and sleep evaluation.Entities:
Keywords: Autoimmune encephalitis; CASPR2-antibodies; Morvan syndrome; Neuroimmunology; Respiratory failure; VGKC-antibodies
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Year: 2020 PMID: 32371280 DOI: 10.1016/j.jns.2020.116865
Source DB: PubMed Journal: J Neurol Sci ISSN: 0022-510X Impact factor: 3.181