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[神经性疼痛作为自主神经病变及其他罕见疾病的一种症状:小纤维神经病变:其识别、诊断与治疗]

[Neuropathic pain as a symptom in autonomic neuropathies and other rare diseases : Small fiber neuropathy: its recognition, diagnosis, and treatment].

作者信息

Fischer Fiona, Dohrn Maike F, Kapfenberger Romina, Igharo Denver, Seeber Diana, de Moya Rubio Elena, Pitarokoili Kalliopi, Börsch Natalie, Mücke Martin, Rolke Roman, Schulz Jörg B, Maier Andrea

机构信息

Klinik für Neurologie, Medizinische Fakultät, RWTH Aachen, Aachen, Deutschland.

Hals-Nasen-Ohren-Klinik, Helios Klinikum Krefeld, Krefeld, Deutschland.

出版信息

Schmerz. 2024 Feb;38(1):33-40. doi: 10.1007/s00482-023-00783-w. Epub 2024 Jan 10.

DOI:10.1007/s00482-023-00783-w
PMID:38197939
Abstract

BACKGROUND

Neuropathic pain is difficult to diagnose and treat. Small fiber neuropathy (SFN) flies under the radar of nerve conduction studies.

OBJECTIVES

The importance of a structured patient history and physical examination in the context of neuropathic pain is emphasized. Describing SFN as an important cause, the authors consider rare but partially treatable differential diagnoses. They conclude that autonomic symptoms are frequently associated, often presenting with diverse symptoms.

METHODS

A selective literature research to present SFN symptoms as well as differential diagnostic and therapeutic steps in the context of SFN and rare diseases focusing on the autonomic nervous system.

RESULTS

Neuropathic pain significantly reduces quality of life. To shorten the time until diagnosis and to initiate therapy, the authors recommend a structured patient history including sensory plus and minus symptoms and non-specific autonomic signs. If the initial search for the cause is not successful, rare causes such as treatable transthyretin (ATTR) amyloidosis and Fabry's disease or autoimmune causes should be considered, particularly in the case of progressive and/or autonomic symptoms.

CONCLUSION

The diagnosis and therapy of rare SFN requires interdisciplinary collaboration and, in many cases, a referral to specialized centers to achieve the best patient care.

摘要

背景

神经性疼痛难以诊断和治疗。小纤维神经病变(SFN)在神经传导研究中未被重视。

目的

强调在神经性疼痛背景下进行结构化病史采集和体格检查的重要性。作者将SFN描述为一个重要病因,并考虑了罕见但部分可治疗的鉴别诊断。他们得出结论,自主神经症状常与之相关,且症状多样。

方法

进行选择性文献研究,以呈现SFN症状以及在SFN和关注自主神经系统的罕见疾病背景下的鉴别诊断和治疗步骤。

结果

神经性疼痛显著降低生活质量。为缩短诊断时间并启动治疗,作者建议进行结构化病史采集,包括感觉症状的增减和非特异性自主神经体征。如果初步病因查找未成功,应考虑罕见病因,如可治疗的转甲状腺素蛋白(ATTR)淀粉样变性和法布里病或自身免疫性病因,特别是在出现进行性和/或自主神经症状的情况下。

结论

罕见SFN的诊断和治疗需要跨学科合作,且在许多情况下,需转诊至专业中心以实现最佳的患者护理。

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本文引用的文献

1
Nonregional small fibre neuropathy in cases of autoimmune autonomic neuropathy.自身免疫性自主神经病中的非区域性小纤维神经病。
J Neurol. 2022 Dec;269(12):6648-6654. doi: 10.1007/s00415-022-11340-3. Epub 2022 Sep 9.
2
Postural orthostatic tachycardia syndrome (POTS): State of the science and clinical care from a 2019 National Institutes of Health Expert Consensus Meeting - Part 1.体位性心动过速综合征(POTS):2019 年美国国立卫生研究院专家共识会议的科学现状和临床护理 - 第 1 部分。
Auton Neurosci. 2021 Nov;235:102828. doi: 10.1016/j.autneu.2021.102828. Epub 2021 Jun 5.
3
Quantitative sensory testing predicts histological small fiber neuropathy in postural tachycardia syndrome.
定量感觉测试可预测体位性心动过速综合征中的组织学小纤维神经病变。
Neurol Clin Pract. 2020 Oct;10(5):428-434. doi: 10.1212/CPJ.0000000000000770.
4
Targeting transthyretin - Mechanism-based treatment approaches and future perspectives in hereditary amyloidosis.靶向甲状腺素运载蛋白——遗传性淀粉样变性的基于机制的治疗方法和未来展望。
J Neurochem. 2021 Mar;156(6):802-818. doi: 10.1111/jnc.15233. Epub 2020 Dec 3.
5
Idiopathic distal sensory polyneuropathy: ACTTION diagnostic criteria.特发性远端感觉性多发性神经病:ACTTION 诊断标准。
Neurology. 2020 Dec 1;95(22):1005-1014. doi: 10.1212/WNL.0000000000010988. Epub 2020 Oct 14.
6
Chance or challenge, spoilt for choice? New recommendations on diagnostic and therapeutic considerations in hereditary transthyretin amyloidosis with polyneuropathy: the German/Austrian position and review of the literature.机遇还是挑战,难以抉择?遗传性转甲状腺素蛋白淀粉样变性多发性神经病诊断与治疗考量的新建议:德国/奥地利立场及文献综述
J Neurol. 2021 Oct;268(10):3610-3625. doi: 10.1007/s00415-020-09962-6. Epub 2020 Jun 4.
7
Canadian Cardiovascular Society Position Statement on Postural Orthostatic Tachycardia Syndrome (POTS) and Related Disorders of Chronic Orthostatic Intolerance.加拿大心血管学会关于体位性心动过速综合征(POTS)和慢性直立不耐受相关障碍的立场声明。
Can J Cardiol. 2020 Mar;36(3):357-372. doi: 10.1016/j.cjca.2019.12.024.
8
Diagnostic criteria for small fibre neuropathy in clinical practice and research.临床实践和研究中小纤维神经病的诊断标准。
Brain. 2019 Dec 1;142(12):3728-3736. doi: 10.1093/brain/awz333.
9
Scientific Advances in and Clinical Approaches to Small-Fiber Polyneuropathy: A Review.小纤维多发性神经病的科学进展与临床治疗方法:综述
JAMA Neurol. 2019 Oct 1;76(10):1240-1251. doi: 10.1001/jamaneurol.2019.2917.
10
The face of postural tachycardia syndrome - insights from a large cross-sectional online community-based survey.姿势性心动过速综合征的特征——来自大型横断面在线社区为基础的调查的见解。
J Intern Med. 2019 Oct;286(4):438-448. doi: 10.1111/joim.12895. Epub 2019 Apr 16.