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Neurology of COVID-19 in Singapore.新加坡2019冠状病毒病的神经学研究
J Neurol Sci. 2020 Nov 15;418:117118. doi: 10.1016/j.jns.2020.117118. Epub 2020 Sep 3.
2
Dysautonomia: An Overlooked Neurological Manifestation in a Critically ill COVID-19 Patient.自主神经功能障碍:危重症COVID-19患者中被忽视的神经学表现
Am J Med Sci. 2020 Oct;360(4):427-429. doi: 10.1016/j.amjms.2020.07.022. Epub 2020 Jul 17.
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Neurologic manifestations in hospitalized patients with COVID-19: The ALBACOVID registry.新型冠状病毒肺炎住院患者的神经系统表现:ALBACOVID注册研究
Neurology. 2020 Aug 25;95(8):e1060-e1070. doi: 10.1212/WNL.0000000000009937. Epub 2020 Jun 1.
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Autoimmune autonomic disorders.自身免疫性自主神经疾病。
Handb Clin Neurol. 2016;133:405-16. doi: 10.1016/B978-0-444-63432-0.00022-0.
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Introduction to autoimmune neurology.自身免疫性神经病学导论
Handb Clin Neurol. 2016;133:3-14. doi: 10.1016/B978-0-444-63432-0.00001-3.
6
DPPX potassium channel antibody: frequency, clinical accompaniments, and outcomes in 20 patients.二肽基肽酶样蛋白6钾通道抗体:20例患者的发生率、临床伴随症状及预后
Neurology. 2014 Nov 11;83(20):1797-803. doi: 10.1212/WNL.0000000000000991. Epub 2014 Oct 15.
7
Immunotherapy trial as diagnostic test in evaluating patients with presumed autoimmune gastrointestinal dysmotility.免疫疗法试验作为诊断测试用于评估疑似自身免疫性胃肠动力障碍患者。
Neurogastroenterol Motil. 2014 Sep;26(9):1285-97. doi: 10.1111/nmo.12391. Epub 2014 Jul 20.
8
Ganglionic acetylcholine receptor autoantibody: oncological, neurological, and serological accompaniments.神经节乙酰胆碱受体自身抗体:肿瘤学、神经学及血清学伴随情况。
Arch Neurol. 2009 Jun;66(6):735-41. doi: 10.1001/archneurol.2009.78.
9
Serologic profiles aiding the diagnosis of autoimmune gastrointestinal dysmotility.有助于诊断自身免疫性胃肠动力障碍的血清学特征。
Clin Gastroenterol Hepatol. 2008 Sep;6(9):988-92. doi: 10.1016/j.cgh.2008.04.009. Epub 2008 Jul 2.
10
Passive transfer of autoimmune autonomic neuropathy to mice.自身免疫性自主神经病变向小鼠的被动转移。
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感染 SARS-CoV-2 后出现的自身免疫性胃肠动力障碍经静脉注射免疫球蛋白成功治疗。

Autoimmune gastrointestinal dysmotility following SARS-CoV-2 infection successfully treated with intravenous immunoglobulin.

机构信息

Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.

Division of Pediatric Gastroenterology, Hepatology and Nutrition, Columbia University Vagelos College of Physicians and Surgeons, New York, New York, USA.

出版信息

Neurogastroenterol Motil. 2022 Jul;34(7):e14314. doi: 10.1111/nmo.14314. Epub 2022 Jan 4.

DOI:10.1111/nmo.14314
PMID:34984765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9257846/
Abstract

BACKGROUND

Autoimmune gastrointestinal dysmotility (AGID) is a limited form of dysautonomia that can be paraneoplastic or idiopathic. Some presentations can be preceded by a viral infection.

METHODS

We report a case of a 17-year-old girl that developed intractable nausea and early satiety after SARS-CoV-2 infection.

KEY RESULTS

Over ten months, she required nasogastric and nasoduodenal tube feedings and finally was advanced to total parenteral nutrition to meet her caloric needs. Her α3 nicotinic ganglionic acetylcholine and anti-striational antibodies were mildly elevated. Gastrointestinal transit scintigraphy studies showed delayed gastric emptying and slowed small bowel transit. Thermoregulatory sweat test showed areas of anhidrosis consistent with autonomic sudomotor impairment. After IVIG treatment the patient's symptoms improved dramatically and she was able to tolerate full oral diet. This was reflected by improvement of her baseline transit studies and the thermoregulatory sweat test.

CONCLUSIONS AND INFERENCES

This is the first report of AGID occurring after SARS-CoV-2 infection. The dramatic response to IVIG emphasizes the importance of early recognition and the reversible and treatable nature of this condition.

摘要

背景

自身免疫性胃肠动力障碍(AGID)是一种局限性自主神经功能障碍,可继发于肿瘤或特发性疾病。某些表现可能先于病毒感染。

方法

我们报告了一例 17 岁女孩在感染 SARS-CoV-2 后出现难治性恶心和早饱。

主要结果

在十个月的时间里,她需要经鼻胃管和经鼻十二指肠管喂养,最终需要全胃肠外营养以满足其热量需求。她的α3 烟碱型乙酰胆碱和抗横纹肌抗体轻度升高。胃肠传输闪烁显像研究显示胃排空延迟和小肠传输减慢。体温调节出汗试验显示无汗区,提示自主副交感神经运动功能障碍。静脉注射免疫球蛋白(IVIG)治疗后,患者症状显著改善,能够耐受全口服饮食。这反映在她的基础转运研究和体温调节出汗试验的改善上。

结论和推断

这是首例 SARS-CoV-2 感染后发生 AGID 的报告。IVIG 的显著疗效强调了早期识别的重要性,以及这种情况具有可逆性和可治疗性。