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多灶性和全身性周围神经病中的肥厚性神经束膜发育异常

Hypertrophic perineurial dysplasia in multifocal and generalized peripheral neuropathies.

作者信息

Thomas P K, King R H, Workman J M, Schröder J M

机构信息

University Department of Clinical Neurology, Institute of Neurology, London, UK.

出版信息

Neuropathol Appl Neurobiol. 2000 Dec;26(6):536-43. doi: 10.1046/j.0305-1846.2000.00289.x.

Abstract

Two cases are described, one with a multifocal cranial and limb neuropathy of adult onset associated with optic neuropathy, and the other with a diffuse demyelinating neuropathy characterized by congenital cataract, mental retardation and progressive lower limb paresis with an onset in childhood. Extensive investigation in both failed to establish the causation. No family history of similar disorder was obtained in either case. Nerve biopsy in both showed similar perineurial abnormalities, the endoneurium being compartmentalized by hypertrophic perineurial cells that exhibited dysplastic features. The appearances resemble those described in a previously reported case of multifocal neuropathy and probably represent an unusual but non-specific response to a peripheral neuropathy.

摘要

本文描述了两个病例,一例为成年起病的多灶性颅神经和肢体神经病合并视神经病变,另一例为弥漫性脱髓鞘性神经病,其特征为先天性白内障、智力发育迟缓以及儿童期起病的进行性下肢轻瘫。对两例患者均进行了广泛检查,但未能明确病因。两例均未获得类似疾病的家族史。两例患者的神经活检均显示类似的神经束膜异常,神经内膜被表现出发育异常特征的肥大神经束膜细胞分隔。这些表现类似于先前报道的一例多灶性神经病,可能代表了对周围神经病的一种不寻常但非特异性反应。

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