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Anti-N-methyl-D-aspartate-receptor encephalitis: diagnosis, optimal management, and challenges
OBJECTIVE: Anti-N-methyl-D-aspartate-receptor (NMDA-R) encephalitis is a new autoimmune disorder, often paraneoplastic in nature, presenting with complex neuropsychiatric symptoms. Diagnosed serologically, this disorder is often responsive to immunosuppressant treatment. The objective of this review...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085332/ https://www.ncbi.nlm.nih.gov/pubmed/25061311 http://dx.doi.org/10.2147/TCRM.S61967 |
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author | Mann, Andrea P Grebenciucova, Elena Lukas, Rimas V |
author_facet | Mann, Andrea P Grebenciucova, Elena Lukas, Rimas V |
author_sort | Mann, Andrea P |
collection | PubMed |
description | OBJECTIVE: Anti-N-methyl-D-aspartate-receptor (NMDA-R) encephalitis is a new autoimmune disorder, often paraneoplastic in nature, presenting with complex neuropsychiatric symptoms. Diagnosed serologically, this disorder is often responsive to immunosuppressant treatment. The objective of this review is to educate clinicians on the challenges of diagnosis and management of this disorder. MATERIALS AND METHODS: A review of the relevant literature on clinical presentation, pathophysiology, and recommended management was conducted using a PubMed search. Examination of the results identified articles published between 2007 and 2014. RESULTS: The literature highlights the importance of recognizing early common signs and symptoms, which include hallucinations, seizures, altered mental status, and movement disorders, often in the absence of fever. Although the presence of blood and/or cerebrospinal fluid autoantibodies confirms diagnosis, approximately 15% of patients have only positive cerebrospinal fluid titers. Antibody detection should prompt a search for an underlying teratoma or other underlying neoplasm and the initiation of first-line immunosuppressant therapy: intravenous methylprednisolone, intravenous immunoglobulin, or plasmapheresis, or a combination thereof. Second-line treatment with rituximab or cyclophosphamide should be implemented if no improvement is noted after 10 days. Complications can include behavioral problems (eg, aggression and insomnia), hypoventilation, catatonia, and autonomic instability. Those patients who can be managed outside an intensive care unit and whose tumors are identified and removed typically have better rates of remission and functional outcomes. CONCLUSION: There is an increasing need for clinicians of different specialties, including psychiatrists, neurologists, oncologists, neurooncologists, immunologists, and intensivists to become familiar with this disorder and its potential complications. Remission can be optimized with prompt detection and aggressive, collaborative treatment within a multidisciplinary team. |
format | Online Article Text |
id | pubmed-4085332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40853322014-07-24 Anti-N-methyl-D-aspartate-receptor encephalitis: diagnosis, optimal management, and challenges Mann, Andrea P Grebenciucova, Elena Lukas, Rimas V Ther Clin Risk Manag Review OBJECTIVE: Anti-N-methyl-D-aspartate-receptor (NMDA-R) encephalitis is a new autoimmune disorder, often paraneoplastic in nature, presenting with complex neuropsychiatric symptoms. Diagnosed serologically, this disorder is often responsive to immunosuppressant treatment. The objective of this review is to educate clinicians on the challenges of diagnosis and management of this disorder. MATERIALS AND METHODS: A review of the relevant literature on clinical presentation, pathophysiology, and recommended management was conducted using a PubMed search. Examination of the results identified articles published between 2007 and 2014. RESULTS: The literature highlights the importance of recognizing early common signs and symptoms, which include hallucinations, seizures, altered mental status, and movement disorders, often in the absence of fever. Although the presence of blood and/or cerebrospinal fluid autoantibodies confirms diagnosis, approximately 15% of patients have only positive cerebrospinal fluid titers. Antibody detection should prompt a search for an underlying teratoma or other underlying neoplasm and the initiation of first-line immunosuppressant therapy: intravenous methylprednisolone, intravenous immunoglobulin, or plasmapheresis, or a combination thereof. Second-line treatment with rituximab or cyclophosphamide should be implemented if no improvement is noted after 10 days. Complications can include behavioral problems (eg, aggression and insomnia), hypoventilation, catatonia, and autonomic instability. Those patients who can be managed outside an intensive care unit and whose tumors are identified and removed typically have better rates of remission and functional outcomes. CONCLUSION: There is an increasing need for clinicians of different specialties, including psychiatrists, neurologists, oncologists, neurooncologists, immunologists, and intensivists to become familiar with this disorder and its potential complications. Remission can be optimized with prompt detection and aggressive, collaborative treatment within a multidisciplinary team. Dove Medical Press 2014-07-01 /pmc/articles/PMC4085332/ /pubmed/25061311 http://dx.doi.org/10.2147/TCRM.S61967 Text en © 2014 Mann et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Mann, Andrea P Grebenciucova, Elena Lukas, Rimas V Anti-N-methyl-D-aspartate-receptor encephalitis: diagnosis, optimal management, and challenges |
title | Anti-N-methyl-D-aspartate-receptor encephalitis: diagnosis, optimal management, and challenges |
title_full | Anti-N-methyl-D-aspartate-receptor encephalitis: diagnosis, optimal management, and challenges |
title_fullStr | Anti-N-methyl-D-aspartate-receptor encephalitis: diagnosis, optimal management, and challenges |
title_full_unstemmed | Anti-N-methyl-D-aspartate-receptor encephalitis: diagnosis, optimal management, and challenges |
title_short | Anti-N-methyl-D-aspartate-receptor encephalitis: diagnosis, optimal management, and challenges |
title_sort | anti-n-methyl-d-aspartate-receptor encephalitis: diagnosis, optimal management, and challenges |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085332/ https://www.ncbi.nlm.nih.gov/pubmed/25061311 http://dx.doi.org/10.2147/TCRM.S61967 |
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