Atypical presentation of an elderly male with autoimmune encephalitis: anti-LG1 limbic encephalitis.

Limbic encephalitis anti-LG1 encephalitis autoimmune encephalitis

Journal

Journal of community hospital internal medicine perspectives
ISSN: 2000-9666
Titre abrégé: J Community Hosp Intern Med Perspect
Pays: United States
ID NLM: 101601396

Informations de publication

Date de publication:
02 Aug 2020
Historique:
entrez: 28 8 2020
pubmed: 28 8 2020
medline: 28 8 2020
Statut: epublish

Résumé

We present a case of an elderly male with anti-LG1 limbic encephalitis involving hypothalamus presenting with acute changes in mental status and persistent hyperthermia. A 74-year-old male presented to the hospital with fever and chills. He had also been evaluated by his PCP for changes in his mental status, trouble remembering things, and following directions while driving. A lumbar puncture was performed, and empiric meningitis coverage was initiated. His LP results were not suggestive for any infectious process. An MRI showed bilateral hippocampal edema. As an infectious workup was non-revealing and other causes were ruled out, with the concern for paraneoplastic or autoimmune encephalitis, patient was started on high dose steroids and plasma exchange while results of antibodies for autoimmune and paraneoplastic encephalitis were awaited. After plasmapheresis and a course of steroids, the patient's mental status began to slowly improve. He was discharged from the hospital and on subsequent neurology office visit, his serum autoimmune encephalitis panel returned positive for anti-LGI 1 antibodies. Further management consisted of outpatient rituximab infusion. Diagnosis of limbic encephalitis can be challenging and can present with symptoms of limbic dysfunction. A modest index of suspicion of limbic encephalitis should be kept in adults with altered mental changes. Early recognition and initiation of therapy can be crucial in the management of patients with autoimmune encephalitis and can prevent permanent cognitive impairment and damage.

Identifiants

pubmed: 32850103
doi: 10.1080/20009666.2020.1785160
pii: 1785160
pmc: PMC7427439
doi:

Types de publication

Case Reports

Langues

eng

Pagination

377-379

Informations de copyright

© 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest.

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Auteurs

Binita Bhandari (B)

Department of Medicine, UPMC Pinnacle, Harrisburg, PA, USA.

Bikash Basyal (B)

Department of Medicine, Abington Jefferson Health, Abington, PA, USA.

Selin Sendil (S)

Department of Medicine, UPMC Pinnacle, Harrisburg, PA, USA.

Resha Khanal (R)

Department of Medicine, UPMC Pinnacle, Harrisburg, PA, USA.

Sunita Neupane (S)

Department of Medicine, UPMC Pinnacle, Harrisburg, PA, USA.

Vinod Nookala (V)

Department of Medicine, UPMC Pinnacle, Harrisburg, PA, USA.

Classifications MeSH