首页> 外文期刊>Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology >Symptom duration and clinical features in painful sensory neuropathy with and without nerve conduction abnormalities.
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Symptom duration and clinical features in painful sensory neuropathy with and without nerve conduction abnormalities.

机译:伴或不伴神经传导异常的疼痛感觉神经病的症状持续时间和临床特征。

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摘要

BACKGROUND: The term "small fiber sensory neuropathy" (SFSN) refers to an axonal sensory polyneuropathy predominantly affecting cutaneous sensory modalities, often associated with pain and with no evidence of large fiber involvement. We hypothesized that, in most patients, SFSN is the earliest manifestation of a nonspecific axonal neuropathy and will usually progress to involve larger, heavily myelinated sensory and motor fibers. We sought indirect evidence of this through an analysis of the correlation between symptom duration and large fiber involvement in patients with painful sensory neuropathy (PSN). METHODS: A clinical diagnosis of PSN was supported by nerve conduction studies or measurement of epidermal nerve fiber (ENF) density in 43 patients. Symptom duration was correlated with the frequency of large fiber loss as measured by nerve conduction abnormalities. The severity and extent of clinical signs and symptoms were also evaluated in subjects with and without electrodiagnostic abnormalities. RESULTS: Patients with large sensory axon involvement had symptoms of longer duration than patients with SFSN. The frequency of electrodiagnostic abnormalities increased in direct proportion to disease duration. Patients with electrodiagnostic abnormalities also had more extensive pinprick sensory deficits, suggesting that small fiber loss was more advanced in this group as well. CONCLUSIONS: In PSN, the incidence of large fiber involvement appears to increase in proportion to symptom duration. This represents indirect evidence that SFSN usually progresses to involve both large and small fibers within 2-10 years.
机译:背景:术语“小纤维感觉神经病”(SFSN)是指主要影响皮肤感觉方式的轴突感觉多发性神经病,通常与疼痛有关,并且没有大纤维受累的证据。我们假设,在大多数患者中,SFSN是非特异性轴突神经病的最早表现,通常会进展为涉及较大的,严重有髓的感觉和运动纤维。我们通过对疼痛感觉神经病(PSN)患者症状持续时间与大纤维受累之间的相关性进行分析,以寻求间接证据。方法:43例神经传导研究或表皮神经纤维(ENF)密度的测定支持了PSN的临床诊断。症状持续时间与通过神经传导异常测量的大量纤维丢失的频率相关。在有或没有电诊断异常的受试者中,还评估了临床体征和症状的严重程度和程度。结果:感觉轴突受累的患者的症状持续时间长于SFSN患者。电诊断异常的频率与疾病持续时间成正比。患有电诊断异常的患者还存在更广泛的针刺感觉缺陷,这表明该组的小纤维丢失也更为严重。结论:在PSN中,大纤维受累的发生率似乎与症状持续时间成正比。这代表了间接证据,表明SFSN通常在2-10年内逐渐涉及​​大,小纤维。

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