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原发性干燥综合征中的周围神经病变:一项基于人群的研究。

Peripheral neuropathy in primary sjogren syndrome: a population-based study.

作者信息

Gøransson Lasse G, Herigstad Anita, Tjensvoll Anne B, Harboe Erna, Mellgren Svein I, Omdal Roald

机构信息

Clinical Immunology Unit, Department of Internal Medicine, Stavanger University Hospital, Stavanger, Norway, Norway.

出版信息

Arch Neurol. 2006 Nov;63(11):1612-5. doi: 10.1001/archneur.63.11.1612.

Abstract

BACKGROUND

Neurological manifestations appear to be frequently involved in patients with primary Sjögren syndrome (PSS).

OBJECTIVE

To investigate the involvement of the peripheral nervous system, including small-diameter nerve fibers, in an unselected cohort of patients who fulfilled the new international criteria for PSS.

DESIGN

Cross-sectional study.

SETTING

Stavanger University Hospital. Patients Sixty-two patients with PSS (mean +/- SD age, 57.1 +/- 14.6 years).

INTERVENTIONS

Clinical neurologic examinations, conventional nerve conduction studies, and skin punch biopsies.

MAIN OUTCOME MEASURES

Signs of large-diameter and small-diameter peripheral nerve fiber neuropathy as determined by clinical examination, nerve conduction studies, and densities of intraepidermal nerve fibers in skin punch biopsy specimens.

RESULTS

Seventeen patients (27%) were diagnosed as having neuropathy after clinical examination. The results of nerve conduction studies were abnormal in 34 patients (55%): 19 patients (31%) had motor neuropathy, 8 (13%) had sensory neuropathy, and 7 (11%) had sensorimotor neuropathy. Two patients had intraepidermal nerve fiber densities less than 3.4 fibers per millimeter, fitting the morphologic criteria for small-diameter nerve fiber neuropathy.

CONCLUSIONS

Peripheral neuropathy occurs in a large proportion of patients with PSS, in most cases as a subclinical demyelinating neuropathy. Small-diameter nerve fiber neuropathy is not a frequent finding in these patients.

摘要

背景

原发性干燥综合征(PSS)患者似乎经常出现神经学表现。

目的

在一组符合PSS新国际标准的未经挑选的患者中,研究包括小直径神经纤维在内的周围神经系统受累情况。

设计

横断面研究。

地点

斯塔万格大学医院。患者62例PSS患者(平均年龄±标准差,57.1±14.6岁)。

干预措施

临床神经学检查、传统神经传导研究和皮肤打孔活检。

主要观察指标

通过临床检查、神经传导研究以及皮肤打孔活检标本中表皮内神经纤维密度来确定大直径和小直径周围神经纤维神经病变的体征。

结果

临床检查后,17例患者(27%)被诊断为患有神经病变。神经传导研究结果显示34例患者(55%)异常:19例患者(31%)有运动神经病变,8例(13%)有感觉神经病变,7例(11%)有感觉运动神经病变。2例患者的表皮内神经纤维密度低于每毫米3.4根纤维,符合小直径神经纤维神经病变的形态学标准。

结论

PSS患者中很大一部分存在周围神经病变,大多数情况下为亚临床脱髓鞘性神经病变。小直径神经纤维神经病变在这些患者中并不常见。

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