Schady W, Goulding P J, Lecky B R, King R H, Smith C M
Department of Neurology, Manchester Royal Infirmary, UK.
J Neurol Neurosurg Psychiatry. 1996 Dec;61(6):636-40. doi: 10.1136/jnnp.61.6.636.
To report three patients with chronic inflammatory demyelinating polyneuropathy (CIDP) presenting with symptoms suggestive of cervical (one patient) and lumbar root disease.
Nerve conduction studies, EMG, and nerve biopsy were carried out, having found the nerve roots to be very enlarged on MRI, CT myelography, and at surgery.
Clinically, peripheral nerve thickening was slight or absent. Subsequently one patient developed facial nerve hypertrophy. This was mistaken for an inner ear tumour and biopsied, with consequent facial palsy. Neurophysiological tests suggested a demyelinating polyneuropathy. Sural nerve biopsy showed in all cases some loss of myelinated fibres, inflammatory cell infiltration, and a few onion bulbs. Hypertrophic changes were much more prominent on posterior nerve root biopsy in one patient: many fibres were surrounded by several layers of Schwann cell cytoplasm. There was an excellent response to steroids in two patients but not in the third (most advanced) patient, who has benefited only marginally from intravenous immunoglobulin therapy.
MRI of the cauda equina may be a useful adjunct in the diagnosis of CIDP.
报告3例慢性炎症性脱髓鞘性多发性神经病(CIDP)患者,其症状提示存在颈神经根病(1例)和腰神经根病。
在通过磁共振成像(MRI)、CT脊髓造影及手术发现神经根明显增粗后,进行了神经传导研究、肌电图(EMG)及神经活检。
临床上,周围神经增粗轻微或无增粗。随后1例患者出现面神经肥大。这被误诊为内耳肿瘤并进行了活检,结果导致面瘫。神经生理学检查提示为脱髓鞘性多发性神经病。所有病例的腓肠神经活检均显示有一些有髓纤维丧失、炎性细胞浸润及少量洋葱球样结构。1例患者后神经根活检的肥大改变更为显著:许多纤维被几层施万细胞胞质所包绕。2例患者对类固醇治疗反应良好,但第3例(病情最严重)患者反应不佳,仅从静脉注射免疫球蛋白治疗中略有获益。
马尾的MRI检查可能是CIDP诊断的一项有用辅助检查。