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本文引用的文献

1
Hyperhidrosis: A Central Nervous Dysfunction of Sweat Secretion.多汗症:一种汗液分泌的中枢神经功能障碍。
Dermatol Ther (Heidelb). 2023 Feb;13(2):453-463. doi: 10.1007/s13555-022-00885-w. Epub 2023 Jan 10.
2
Case Report: Paroxysmal hyperhidrosis as an initial symptom in a patient with anti-LGI1 encephalitis.病例报告:抗 LGI1 脑炎患者以阵发性多汗为首发症状。
Front Immunol. 2022 Sep 23;13:986853. doi: 10.3389/fimmu.2022.986853. eCollection 2022.
3
Clinical Features and Therapeutic Effects of Anti-leucine-rich Glioma Inactivated 1 Encephalitis: A Systematic Review.抗富含亮氨酸胶质瘤失活1脑炎的临床特征及治疗效果:一项系统评价
Front Neurol. 2022 Jan 12;12:791014. doi: 10.3389/fneur.2021.791014. eCollection 2021.
4
Abnormal sweating and "skin flushing" as possible predictive factor for treatment related fluctuations in Guillain-Barré syndrome: a case series and a review of the literature.异常出汗和“皮肤潮红”可能是吉兰-巴雷综合征治疗相关波动的预测因素:病例系列和文献复习。
J Neurol Sci. 2021 Sep 15;428:117589. doi: 10.1016/j.jns.2021.117589. Epub 2021 Jul 25.
5
Autoimmune encephalitis: proposed best practice recommendations for diagnosis and acute management.自身免疫性脑炎:诊断和急性治疗的最佳实践建议。
J Neurol Neurosurg Psychiatry. 2021 Jul;92(7):757-768. doi: 10.1136/jnnp-2020-325300. Epub 2021 Mar 1.
6
Anti-LGI1 Encephalitis Developing Immunoglobulin Responsive Orthostatic Hypotension after Remission.抗 LGI1 脑炎缓解后免疫球蛋白反应性直立性低血压。
Intern Med. 2021 Sep 15;60(18):3021-3024. doi: 10.2169/internalmedicine.5359-20. Epub 2020 Oct 14.
7
Antibody-LGI 1 autoimmune encephalitis manifesting as rapidly progressive dementia and hyponatremia: a case report and literature review.表现为快速进展性痴呆和低钠血症的抗LGI 1自身免疫性脑炎:病例报告及文献复习
BMC Neurol. 2019 Feb 7;19(1):19. doi: 10.1186/s12883-019-1251-4.
8
Treatment of autonomic dysfunction in Parkinson disease and other synucleinopathies.帕金森病和其他突触核蛋白病自主神经功能障碍的治疗。
Mov Disord. 2018 Mar;33(3):372-390. doi: 10.1002/mds.27344.
9
Anti-LGI1 encephalitis: Clinical syndrome and long-term follow-up.抗 LGI1 脑炎:临床综合征和长期随访。
Neurology. 2016 Oct 4;87(14):1449-1456. doi: 10.1212/WNL.0000000000003173. Epub 2016 Sep 2.
10
Focal hyperhidrosis in tumefactive multiple sclerosis.
Arch Neurol. 2010 Nov;67(11):1407-8. doi: 10.1001/archneurol.2010.274.

急性多汗症:潜在自主神经功能障碍及一种罕见神经系统疾病的线索

Acute Hyperhidrosis: A Clue to Underlying Autonomic Dysfunction and a Rare Neurological Disorder.

作者信息

Peh Rachel, Yip Chun Wai, Liew Zhong Hong

机构信息

Internal Medicine, Singapore General Hospital, Singapore, SGP.

Neurology, Singapore General Hospital, Singapore, SGP.

出版信息

Cureus. 2024 Dec 25;16(12):e76387. doi: 10.7759/cureus.76387. eCollection 2024 Dec.

DOI:10.7759/cureus.76387
PMID:39867015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11762238/
Abstract

Acute hyperhidrosis is characterized by excessive sweating. In the absence of other symptoms, the symptoms of sweating alone are often benign and may be ignored by patients and clinicians. Rarely, hyperhidrosis may be a harbinger of an underlying severe disease. Autonomic nervous system dysfunction leading to hyperactivity of the sympathetic nervous system can result in excessive sweating. This case report is about a gentleman who presented with acute hyperhidrosis, a symptom of autonomic dysfunction, which turned out to be a relapse of anti-leucine-rich glioma-inactivated 1 (LGI1) antibody encephalitis. This case adds to the existing literature on cases of anti-LGI-1 encephalitis, a rare form of autoimmune encephalitis, and its varied clinical manifestations. It serves as a reminder to consider a wide range of differentials in patients who present with a seemingly nonspecific complaint such as excessive sweating.

摘要

急性多汗症的特征是出汗过多。在没有其他症状的情况下,仅出汗症状通常是良性的,患者和临床医生可能会忽略。极少数情况下,多汗症可能是潜在严重疾病的先兆。导致交感神经系统功能亢进的自主神经系统功能障碍可导致出汗过多。本病例报告讲述的是一位男性患者,他出现急性多汗症这一自主神经功能障碍症状,结果竟是抗富含亮氨酸胶质瘤失活1(LGI1)抗体脑炎复发。该病例补充了现有关于抗LGI-1脑炎(一种罕见的自身免疫性脑炎形式)及其多样临床表现的文献。它提醒人们,对于出现诸如多汗症这种看似非特异性症状的患者,要考虑多种不同的鉴别诊断。