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Case report: Coexistence of Labbe vein thrombosis and autoimmune encephalitis with two different antibodies
Anti-NMDA receptor encephalitis is an autoimmune encephalitis well- known to pediatric neurologists. The characteristic combination of symptoms and detection of NMDA receptor antibody can confirm the diagnosis. Most children respond well to immunosuppressive therapy. Anti-GABAB receptor encephalitis...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374307/ https://www.ncbi.nlm.nih.gov/pubmed/37521281 http://dx.doi.org/10.3389/fneur.2023.1170169 |
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author | Yang, Lu Zhang, Dongqing |
author_facet | Yang, Lu Zhang, Dongqing |
author_sort | Yang, Lu |
collection | PubMed |
description | Anti-NMDA receptor encephalitis is an autoimmune encephalitis well- known to pediatric neurologists. The characteristic combination of symptoms and detection of NMDA receptor antibody can confirm the diagnosis. Most children respond well to immunosuppressive therapy. Anti-GABAB receptor encephalitis usually occurs in adult patients. Most patients present clinically with symptoms of limbic encephalitis. Cases in pediatric patients are rare. Cerebral venous thrombosis also has a very low incidence in children without underlying diseases. Patients usually present with headaches, convulsions, and focal deficits. Anticoagulants are the first choice treatment. We report a boy initially diagnosed with Labbe vein thrombosis and later tested positive for both NMDA and GABAB receptors. Anticoagulants did not relieve the boy's symptoms, and immunosuppressive therapy achieved good results. The antibody titers were significantly reduced or even turned negative. Although the Labbe vein was not recanalized at four months follow-up, the brain lesion was significantly absorbed. We learn from this case that a child can be inflicted with cerebral venous thrombosis and autoimmune encephalitis simultaneously. Child patients respond well to treatment. |
format | Online Article Text |
id | pubmed-10374307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103743072023-07-28 Case report: Coexistence of Labbe vein thrombosis and autoimmune encephalitis with two different antibodies Yang, Lu Zhang, Dongqing Front Neurol Neurology Anti-NMDA receptor encephalitis is an autoimmune encephalitis well- known to pediatric neurologists. The characteristic combination of symptoms and detection of NMDA receptor antibody can confirm the diagnosis. Most children respond well to immunosuppressive therapy. Anti-GABAB receptor encephalitis usually occurs in adult patients. Most patients present clinically with symptoms of limbic encephalitis. Cases in pediatric patients are rare. Cerebral venous thrombosis also has a very low incidence in children without underlying diseases. Patients usually present with headaches, convulsions, and focal deficits. Anticoagulants are the first choice treatment. We report a boy initially diagnosed with Labbe vein thrombosis and later tested positive for both NMDA and GABAB receptors. Anticoagulants did not relieve the boy's symptoms, and immunosuppressive therapy achieved good results. The antibody titers were significantly reduced or even turned negative. Although the Labbe vein was not recanalized at four months follow-up, the brain lesion was significantly absorbed. We learn from this case that a child can be inflicted with cerebral venous thrombosis and autoimmune encephalitis simultaneously. Child patients respond well to treatment. Frontiers Media S.A. 2023-07-13 /pmc/articles/PMC10374307/ /pubmed/37521281 http://dx.doi.org/10.3389/fneur.2023.1170169 Text en Copyright © 2023 Yang and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Yang, Lu Zhang, Dongqing Case report: Coexistence of Labbe vein thrombosis and autoimmune encephalitis with two different antibodies |
title | Case report: Coexistence of Labbe vein thrombosis and autoimmune encephalitis with two different antibodies |
title_full | Case report: Coexistence of Labbe vein thrombosis and autoimmune encephalitis with two different antibodies |
title_fullStr | Case report: Coexistence of Labbe vein thrombosis and autoimmune encephalitis with two different antibodies |
title_full_unstemmed | Case report: Coexistence of Labbe vein thrombosis and autoimmune encephalitis with two different antibodies |
title_short | Case report: Coexistence of Labbe vein thrombosis and autoimmune encephalitis with two different antibodies |
title_sort | case report: coexistence of labbe vein thrombosis and autoimmune encephalitis with two different antibodies |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374307/ https://www.ncbi.nlm.nih.gov/pubmed/37521281 http://dx.doi.org/10.3389/fneur.2023.1170169 |
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