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小纤维受累于脊髓延髓肌肉萎缩症(肯尼迪病)。

Small-fiber involvement in spinobulbar muscular atrophy (Kennedy's disease).

作者信息

Manganelli Fiore, Iodice Valeria, Provitera Vincenzo, Pisciotta Chiara, Nolano Maria, Perretti Anna, Santoro Lucio

机构信息

Department of Neurological Sciences, University Federico II of Naples, Via Sergio Pansini 5, 80131 Naples, Italy.

出版信息

Muscle Nerve. 2007 Dec;36(6):816-20. doi: 10.1002/mus.20872.

Abstract

We assessed the involvement of cutaneous innervation in two subjects with a molecularly confirmed diagnosis of spinobulbar muscular atrophy (SBMA) using antidromic nerve conduction studies, quantitative sensory testing, and sweat tests, as well as immunohistochemical techniques and confocal microscopy of glabrous and hairy skin biopsy. Both patients showed a marked reduction in amplitude of sensory action potentials and moderate or severe abnormalities of tactile thresholds and mechanical pain perception. A severe reduction of sweat drops on the Silastic imprint test and a widespread loss of small myelinated and unmyelinated fibers in hairy skin were also observed. Fiber loss involved either somatic or autonomic fibers and did not show any distal-proximal gradient. These results, together with loss of Meissner corpuscles and their large myelinated afferent fibers in glabrous skin, confirmed the extensive involvement of sensory neurons of large and small size and revealed an autonomic skin denervation in SBMA.

摘要

我们使用逆向神经传导研究、定量感觉测试和汗液测试,以及无毛和有毛皮肤活检的免疫组织化学技术和共聚焦显微镜,评估了两名经分子确诊的脊髓延髓肌肉萎缩症(SBMA)患者的皮肤神经支配情况。两名患者均表现出感觉动作电位幅度显著降低,触觉阈值和机械性疼痛感知存在中度或重度异常。在硅橡胶印迹试验中还观察到汗滴严重减少,有毛皮肤中小有髓和无髓纤维广泛缺失。纤维丢失涉及躯体或自主神经纤维,未显示任何远端-近端梯度。这些结果,连同无毛皮肤中迈斯纳小体及其大的有髓传入纤维的丢失,证实了大小感觉神经元的广泛受累,并揭示了SBMA中自主皮肤去神经支配。

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