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本文引用的文献

1
Quantification of sweat gland innervation: a clinical-pathologic correlation.汗腺神经支配的定量分析:临床与病理的相关性
Neurology. 2009 Apr 28;72(17):1479-86. doi: 10.1212/WNL.0b013e3181a2e8b8.
2
Evaluation of distal symmetric polyneuropathy: the role of autonomic testing, nerve biopsy, and skin biopsy (an evidence-based review).远端对称性多发性神经病的评估:自主神经检测、神经活检和皮肤活检的作用(循证综述)
Muscle Nerve. 2009 Jan;39(1):106-15. doi: 10.1002/mus.21227.
3
Practice Parameter: evaluation of distal symmetric polyneuropathy: role of autonomic testing, nerve biopsy, and skin biopsy (an evidence-based review) [RETIRED]. Report of the American Academy of Neurology, American Association of Neuromuscular and Electrodiagnostic Medicine, and American Academy of Physical Medicine and Rehabilitation.实践参数:远端对称性多发性神经病的评估:自主神经检测、神经活检和皮肤活检的作用(循证综述)[已退休]。美国神经病学学会、美国神经肌肉与电诊断医学协会及美国物理医学与康复学会报告。
Neurology. 2009 Jan 13;72(2):177-84. doi: 10.1212/01.wnl.0000336345.70511.0f. Epub 2008 Dec 3.
4
Anhidrosis in multiple system atrophy: a preganglionic sudomotor dysfunction?多系统萎缩中的无汗症:节前泌汗功能障碍?
Mov Disord. 2008 Apr 30;23(6):885-8. doi: 10.1002/mds.21972.
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Isolated generalised anhidrosis induced by postganglionic sympathetic skin nerve fibre degeneration: an incomplete Ross syndrome?节后交感皮肤神经纤维变性引起的孤立性全身性无汗症:一种不完全性罗斯综合征?
J Neurol Neurosurg Psychiatry. 2008 Aug;79(8):959-61. doi: 10.1136/jnnp.2007.142802. Epub 2008 Mar 20.
6
Evaluation of cutaneous autonomic innervation in idiopathic sensory small-fiber neuropathy.特发性感觉性小纤维神经病变中皮肤自主神经支配的评估
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7
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J Neural Transm (Vienna). 2006 Sep;113(9):1169-76. doi: 10.1007/s00702-005-0431-0. Epub 2006 Jul 13.
8
Detection of small-fiber neuropathy by sudomotor testing.通过汗腺功能测试检测小纤维神经病变
Muscle Nerve. 2006 Jul;34(1):57-61. doi: 10.1002/mus.20551.
9
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10
The utility of skin biopsy for prediction of progression in suspected small fiber neuropathy.皮肤活检在疑似小纤维神经病变进展预测中的作用。
Neurology. 2006 Jan 24;66(2):256-8. doi: 10.1212/01.wnl.0000194314.86486.a2.

定量评估汗腺神经支配:三种方法的比较。

Quantification of sudomotor innervation: a comparison of three methods.

机构信息

Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, 1 Deaconess Road, Boston, Massachusetts 02215, USA.

出版信息

Muscle Nerve. 2010 Jul;42(1):112-9. doi: 10.1002/mus.21626.

DOI:10.1002/mus.21626
PMID:20544913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3048308/
Abstract

Peripheral sudomotor dysfunction is present in many peripheral neuropathies, but structural assessments of sudomotor fibers rarely occur. We evaluated 36 diabetic and 72 healthy control subjects who underwent detailed neurologic examinations and punch skin biopsies. Physical exam findings were quantified by neuropathy impairment score in the lower limb. Skin biopsies quantified intraepidermal nerve fiber density (IENFD) and sweat gland nerve fiber density (SGNFD) by a manual, automated, and semiquantitative method. The automated and manual SGNFD correlated with the IENFD at the same site (r = 0.62, P < 0.05 automated method, r = 0.67, P < 0.05 manual method). As neuropathy worsened, the SGNFD at the distal leg declined (automated counting r = -0.81, P < 0.001; manual counting r = -0.88, P < 0.001). The semiquantitative method displayed poor inter- and intrareviewer reliability and correlated poorly with standard neuropathy evaluation scores. Our results suggest that sudomotor fibers can be rapidly and reproducibly quantified, and results correlate well with physical exam findings.

摘要

周围性自主运动功能障碍存在于许多周围神经病变中,但很少对自主运动纤维进行结构评估。我们评估了 36 名糖尿病患者和 72 名健康对照者,他们接受了详细的神经检查和皮肤活检。体格检查结果通过下肢神经病变损伤评分进行量化。皮肤活检通过手动、自动和半定量方法定量评估表皮内神经纤维密度(IENFD)和汗腺神经纤维密度(SGNFD)。自动和手动 SGNFD 与同一部位的 IENFD 相关(自动计数 r = 0.62,P < 0.05;手动计数 r = 0.67,P < 0.05)。随着神经病变的恶化,小腿远端的 SGNFD 下降(自动计数 r = -0.81,P < 0.001;手动计数 r = -0.88,P < 0.001)。半定量方法显示出较差的组内和组间可靠性,与标准神经病变评估评分相关性差。我们的结果表明,自主运动纤维可以快速、可重复地定量,并且结果与体格检查结果很好地相关。