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A case of chronic inflammatory demyelinating polyneuropathy presented with unilateral ptosis

机译:慢性炎性脱髓鞘性多发性神经病合并单侧上睑下垂一例

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摘要

Chronic Inflammatory Demyelinating Polyneuropathy is an autoimmune disease with progressive and relapsing courses. The main clinical presentations are diffuse deep tendon hyporeflexia or areflexia and symmetric proximal-distal muscles weakness. Myasthenia gravis is also an immune mediated disease with fluctuating ocular and bulbar symptoms and sometimes weakness. Although both myasthenia gravis and chronic inflammatory demyelinating polyneuropathy are immune mediated disorders, clinical presentations are obviously different in the two diseases. Herein, we will report a case of chronic inflammatory demyelinating polyneuropathy who presented with isolated unilateral ptosis. Initially, the patient was managed as ocular type of myasthenia gravis, but after progression to general limb weakness and areflexia, the diagnosis of chronic inflammatory demyelinating polyneuropathy was made. Although unilateral ptosis is a typical feature of myasthenia gravis, it may be seen as the first presentation of chronic inflammatory demyelinating polyneuropathy as well which mimics myasthenia gravis disease.
机译:慢性炎性脱髓鞘性多发性神经病是一种具有进行性和复发性病程的自身免疫性疾病。主要临床表现为弥漫性深肌腱反射不足或反射消失以及近端-远端对称肌无力。重症肌无力也是一种免疫介导的疾病,其眼和延髓症状波动,有时甚至无力。尽管重症肌无力和慢性炎性脱髓鞘性多神经病都是免疫介导的疾病,但两种疾病的临床表现明显不同。在这里,我们将报告一例慢性炎症性脱髓鞘性多发性神经病,并伴有单侧上睑下垂。最初,该患者以重症肌无力的眼型进行治疗,但在发展为全身四肢无力和反射乏力后,诊断为慢性炎症性脱髓鞘性多发性神经病。尽管单侧上睑下垂是重症肌无力的典型特征,但它可被视为模仿重症肌无力疾病的慢性炎症性脱髓鞘性多发性神经病的首发表现。

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