Cardinali P, Serrao M, Rossi P, De Dominicis L, Logullo F, De Santis F, Pierelli F
City Hospital of Fermo, MC, Italy.
Neurol Sci. 2005 Dec;26(5):344-8. doi: 10.1007/s10072-005-0495-5.
Case of a 58-year-old patient diagnosed as having mycosis fungoides (MF) who presented with sensory ataxia, limbs weakness and neurophysiological and laboratory signs indicative of autoimmune chronic mixed axonal-demyelinating sensory-motor polyradicular neuropathy. The possibility that MF may be associated with an immunomediated peripheral neuropathy, even in the absence of a direct invasion of the nerves and widespread visceral involvement, should be considered.
一名58岁被诊断为蕈样肉芽肿(MF)的患者,出现感觉性共济失调、肢体无力以及提示自身免疫性慢性混合性轴索性-脱髓鞘性感觉运动性多神经根神经病的神经生理学和实验室检查体征。即使在没有神经直接侵犯和广泛内脏受累的情况下,也应考虑MF可能与免疫介导的周围神经病相关。