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Paraneoplastic anti-GAD65 extralimbic encephalitis presented with epilepsy: A case report

RATIONALE: Autoimmunity targeting glutamic acid decarboxylase 65 (GAD65) is associated with type 1 diabetes mellitus as well as various neurological diseases. In the central nervous system, GAD65 autoimmunity usually presents with limbic encephalitis, whereas extralimbic encephalitis (ELE) has only...

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Autores principales: Xia, Si-Qi, Fan, Hao-Nan, Fan, Lin-Feng, Xia, Wu, Chen, Gao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10627632/
https://www.ncbi.nlm.nih.gov/pubmed/37933077
http://dx.doi.org/10.1097/MD.0000000000034780
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author Xia, Si-Qi
Fan, Hao-Nan
Fan, Lin-Feng
Xia, Wu
Chen, Gao
author_facet Xia, Si-Qi
Fan, Hao-Nan
Fan, Lin-Feng
Xia, Wu
Chen, Gao
author_sort Xia, Si-Qi
collection PubMed
description RATIONALE: Autoimmunity targeting glutamic acid decarboxylase 65 (GAD65) is associated with type 1 diabetes mellitus as well as various neurological diseases. In the central nervous system, GAD65 autoimmunity usually presents with limbic encephalitis, whereas extralimbic encephalitis (ELE) has only been reported in a few cases. Moreover, anti-GAD65 ELE in the paraneoplastic context has not yet been reported. PATIENT CONCERNS: A 60-year-old man presented with intermittent cough and sputum for 10 years, with no other diseases. The patient presented with recurrent seizures that were resistant to antiepileptic drugs (AEDs). Chest computed tomography and pathological results confirmed the diagnosis of small cell lung cancer. Paraneoplastic testing found a high level of GAD65 antibodies in his serum, and cerebrospinal fluid analysis revealed lymphocytic pleocytosis, indicating autoimmune encephalitis. Brain magnetic resonance imaging showed multifocal T2 fluid-attenuated inversion recovery hyperintensities in the extralimbic areas including the subcortex and deep white matter of the bilateral frontal lobe, parietal lobe, and insula lobes. DIAGNOSES: Finally, a diagnosis of anti-GAD65 autoimmune ELE with a paraneoplastic etiology from the small cell lung cancer was suspected. INTERVENTIONS: The patient refused any tumor-suppressive treatment or immunotherapy for potential side effects and only received AEDs levetiracetam, sodium valproate, and diazepam. OUTCOMES: The epilepsy of the patient was resistant to AEDs, and the patient died a week after discharge due to disease progression. LESSONS: Anti-GAD65 autoimmune encephalitis can be extralimbic, can present with isolated epilepsy, and extralimbic anti-GAD65 encephalitis can occur with an underlying malignancy.
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spelling pubmed-106276322023-11-07 Paraneoplastic anti-GAD65 extralimbic encephalitis presented with epilepsy: A case report Xia, Si-Qi Fan, Hao-Nan Fan, Lin-Feng Xia, Wu Chen, Gao Medicine (Baltimore) 5300 RATIONALE: Autoimmunity targeting glutamic acid decarboxylase 65 (GAD65) is associated with type 1 diabetes mellitus as well as various neurological diseases. In the central nervous system, GAD65 autoimmunity usually presents with limbic encephalitis, whereas extralimbic encephalitis (ELE) has only been reported in a few cases. Moreover, anti-GAD65 ELE in the paraneoplastic context has not yet been reported. PATIENT CONCERNS: A 60-year-old man presented with intermittent cough and sputum for 10 years, with no other diseases. The patient presented with recurrent seizures that were resistant to antiepileptic drugs (AEDs). Chest computed tomography and pathological results confirmed the diagnosis of small cell lung cancer. Paraneoplastic testing found a high level of GAD65 antibodies in his serum, and cerebrospinal fluid analysis revealed lymphocytic pleocytosis, indicating autoimmune encephalitis. Brain magnetic resonance imaging showed multifocal T2 fluid-attenuated inversion recovery hyperintensities in the extralimbic areas including the subcortex and deep white matter of the bilateral frontal lobe, parietal lobe, and insula lobes. DIAGNOSES: Finally, a diagnosis of anti-GAD65 autoimmune ELE with a paraneoplastic etiology from the small cell lung cancer was suspected. INTERVENTIONS: The patient refused any tumor-suppressive treatment or immunotherapy for potential side effects and only received AEDs levetiracetam, sodium valproate, and diazepam. OUTCOMES: The epilepsy of the patient was resistant to AEDs, and the patient died a week after discharge due to disease progression. LESSONS: Anti-GAD65 autoimmune encephalitis can be extralimbic, can present with isolated epilepsy, and extralimbic anti-GAD65 encephalitis can occur with an underlying malignancy. Lippincott Williams & Wilkins 2023-11-03 /pmc/articles/PMC10627632/ /pubmed/37933077 http://dx.doi.org/10.1097/MD.0000000000034780 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 5300
Xia, Si-Qi
Fan, Hao-Nan
Fan, Lin-Feng
Xia, Wu
Chen, Gao
Paraneoplastic anti-GAD65 extralimbic encephalitis presented with epilepsy: A case report
title Paraneoplastic anti-GAD65 extralimbic encephalitis presented with epilepsy: A case report
title_full Paraneoplastic anti-GAD65 extralimbic encephalitis presented with epilepsy: A case report
title_fullStr Paraneoplastic anti-GAD65 extralimbic encephalitis presented with epilepsy: A case report
title_full_unstemmed Paraneoplastic anti-GAD65 extralimbic encephalitis presented with epilepsy: A case report
title_short Paraneoplastic anti-GAD65 extralimbic encephalitis presented with epilepsy: A case report
title_sort paraneoplastic anti-gad65 extralimbic encephalitis presented with epilepsy: a case report
topic 5300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10627632/
https://www.ncbi.nlm.nih.gov/pubmed/37933077
http://dx.doi.org/10.1097/MD.0000000000034780
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