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首页> 外文期刊>Acta Neuropathologica >Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) with hypertrophic spinal radiculopathy mimicking neurofibromatosis
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Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) with hypertrophic spinal radiculopathy mimicking neurofibromatosis

机译:慢性发炎性脱髓鞘性多发性神经根病(CIDP),伴有神经纤维瘤病的肥厚性脊神经根病

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摘要

This report illustrates a case of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) masquerading as neurofibromatosis due to multifocal enlargements of spinal nerve roots. The patient initially complained of intermittent numbness of the hands and leg weakness at age 62. Nerve conduction velocities were reported to be abnormally slow, suggesting a diagnosis of demyelinating neuropathy. A complaint of progressive lower back pain 4 years later prompted a lumbar CT myelogram, which demonstrated bilateral nerve root enlargements. A biopsy of an enlarged lumbar root obtained during decompressive laminectomy was interpreted as consistent with a plexiform neurofibroma. He suffered recurrent paraparesis, at times with a sensory level indicating spinal cord compression, which responded to corticosteroid therapy. An autopsy 15 years after the onset of symptoms revealed hypertrophic radiculopathy and peripheral neuropathy due to CIDP with no evidence of neurofibromatosis. This case illustrates how the hypertrophic neuropathy accompanying CIDP can be mistaken for neurofibromatosis.
机译:该报告说明了由于脊髓神经根的多灶性增生而伪装成神经纤维瘤病的慢性炎症性脱髓鞘性多发性神经根病(CIDP)。该患者最初主诉62岁时断断续续的手和腿无力麻木。据报道,神经传导速度异常缓慢,提示诊断为脱髓鞘性神经病。 4年后出现进行性下腰痛的主诉提示腰部CT脊髓造影,显示双侧神经根肿大。减压椎板切除术中获得的扩大的腰根活检被解释为与丛状神经纤维瘤一致。他患有反复性轻瘫,有时感觉水平表明脊髓受压,这对皮质类固醇激素疗法有反应。症状发作后15年的尸检显示,由于CIDP导致肥厚性神经根病变和周围神经病变,没有神经纤维瘤病的证据。这种情况说明了如何将伴随CIDP的肥大性神经病误认为是神经纤维瘤病。

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