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臂丛神经局限性肥厚性神经病:MRI诊断及术前评估

[Localized hypertrophic neuropathy (LHN) of the brachial plexus: diagnosis and presurgical evaluation with MRI].

作者信息

Saguintaah M, Veyrac C, Baud C, Couture A

机构信息

Service de Radiologie Pédiatrique, Hôpital Arnaud de Villeneuve, 34295 Montpellier Cedex 5, France.

出版信息

J Radiol. 2002 Jun;83(6 Pt 1):745-7.

Abstract

The authors report a case of localized hypertrophic neuropathy diagnosed by MRI. This 10-year-old girl presented with painless progressive deltoid atrophy. Electrodiagnostic studies demonstrated chronic denervation. An MRI performed with T1, T2, T1 with gadolinium and fat saturation sequences showed a linear 5-cm long segment of hypertrophic brachial plexus cord, with moderate high T2, intermediate T1 signal, and marked post-Gadolinium enhancement. Progressive improvement followed surgical resection with nerve graft repair. Histological study confirmed LHN (perineurial cell proliferation), a rare cause of peripheral neurological deficit. MRI findings may suggest LHN, that should be suspected as well as peripheral nerve compression or tumor; inflammatory neuritis and idiopathic lesion (with normal MRI findings) remain a diagnosis of exclusion. MR aids in the precise localization of the lesion before surgery.

摘要

作者报告了一例通过MRI诊断的局限性肥厚性神经病。这名10岁女孩表现为无痛性进行性三角肌萎缩。电诊断研究显示为慢性去神经支配。采用T1、T2、钆增强T1及脂肪抑制序列进行的MRI检查显示,臂丛神经索有一段5厘米长的线性肥厚节段,T2呈中度高信号,T1呈中等信号,钆增强后有明显强化。手术切除并进行神经移植修复后病情逐渐改善。组织学研究证实为局限性肥厚性神经病(神经束膜细胞增殖),这是导致周围神经功能缺损的一种罕见原因。MRI表现可能提示局限性肥厚性神经病,对此应与周围神经受压或肿瘤一样予以怀疑;炎症性神经炎和特发性病变(MRI表现正常)仍是排除性诊断。MRI有助于在手术前精确确定病变位置。

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