Case Report: Refractory Hypotension of GABA B Receptor Autoimmune Encephalitis
Introduction: With the development of antibody detection technology, Gamma-Aminobutyric Acid (GABA) B receptor encephalitis is a known autoimmune disease. This paper describes a patient with refractory hypotension who suffered GABA B receptor autoimmune encephalitis.Case Report: We describe a 63-yea...
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2020-12-01
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doaj-08e20d74b5c94848aab371065cdb4bb32020-12-08T08:38:05ZengFrontiers Media S.A.Frontiers in Neurology1664-22952020-12-011110.3389/fneur.2020.571382571382Case Report: Refractory Hypotension of GABA B Receptor Autoimmune EncephalitisKong Hanxin0Wang Xiaomin1Ying Hao2Zheng Shuihong3Jinhua Central Hospital, Jinhua, ChinaJinhua Central Hospital, Jinhua, ChinaYuhang First People's Hospital, Hangzhou, ChinaJinhua Central Hospital, Jinhua, ChinaIntroduction: With the development of antibody detection technology, Gamma-Aminobutyric Acid (GABA) B receptor encephalitis is a known autoimmune disease. This paper describes a patient with refractory hypotension who suffered GABA B receptor autoimmune encephalitis.Case Report: We describe a 63-year-old man with GABA B receptor autoimmune encephalitis who had hypotension on day 17 of the disease onset. Despite two rounds of immunoglobulin administration, high-dose intravenous steroid injections and immunosuppressive therapy on day 35 of hospitalization, psychiatric symptoms and seizures were significantly improved; however, the patient's blood pressure remained low.Conclusion: This case study and literature review investigated the impairment of autonomic nerve function and its subsequent management in patients with GABA B receptor autoimmune encephalitis.https://www.frontiersin.org/articles/10.3389/fneur.2020.571382/fullGABA B receptor autoimmune encephalitisrefractory hypotensionautonomic nerve functionautoimmune diseasecase report |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kong Hanxin Wang Xiaomin Ying Hao Zheng Shuihong |
spellingShingle |
Kong Hanxin Wang Xiaomin Ying Hao Zheng Shuihong Case Report: Refractory Hypotension of GABA B Receptor Autoimmune Encephalitis Frontiers in Neurology GABA B receptor autoimmune encephalitis refractory hypotension autonomic nerve function autoimmune disease case report |
author_facet |
Kong Hanxin Wang Xiaomin Ying Hao Zheng Shuihong |
author_sort |
Kong Hanxin |
title |
Case Report: Refractory Hypotension of GABA B Receptor Autoimmune Encephalitis |
title_short |
Case Report: Refractory Hypotension of GABA B Receptor Autoimmune Encephalitis |
title_full |
Case Report: Refractory Hypotension of GABA B Receptor Autoimmune Encephalitis |
title_fullStr |
Case Report: Refractory Hypotension of GABA B Receptor Autoimmune Encephalitis |
title_full_unstemmed |
Case Report: Refractory Hypotension of GABA B Receptor Autoimmune Encephalitis |
title_sort |
case report: refractory hypotension of gaba b receptor autoimmune encephalitis |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Neurology |
issn |
1664-2295 |
publishDate |
2020-12-01 |
description |
Introduction: With the development of antibody detection technology, Gamma-Aminobutyric Acid (GABA) B receptor encephalitis is a known autoimmune disease. This paper describes a patient with refractory hypotension who suffered GABA B receptor autoimmune encephalitis.Case Report: We describe a 63-year-old man with GABA B receptor autoimmune encephalitis who had hypotension on day 17 of the disease onset. Despite two rounds of immunoglobulin administration, high-dose intravenous steroid injections and immunosuppressive therapy on day 35 of hospitalization, psychiatric symptoms and seizures were significantly improved; however, the patient's blood pressure remained low.Conclusion: This case study and literature review investigated the impairment of autonomic nerve function and its subsequent management in patients with GABA B receptor autoimmune encephalitis. |
topic |
GABA B receptor autoimmune encephalitis refractory hypotension autonomic nerve function autoimmune disease case report |
url |
https://www.frontiersin.org/articles/10.3389/fneur.2020.571382/full |
work_keys_str_mv |
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