系统性红斑狼疮伴血管性多神经病变的不典型表现

G. Kadam, Janakraj Deshmukh, D. Ruikar, Amar Limbapure, D. Patil
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摘要

一例22岁的系统性红斑狼疮(SLE)女性患者,无明显病史,无合并症,主诉为双侧下肢急性疼痛和烧灼感,主要累及鞋底和足部,并有脱发和马尔疹病史。经评估,她的生命体征稳定,存在足部水肿,心血管、呼吸、腹部系统未见明显异常。神经学检查显示双侧踝关节反射缺失。双侧足底屈曲,感觉改变,双侧下肢本体感觉和关节感觉减弱。对她的上述抱怨和检查结果进行评估。神经传导研究显示严重的感觉运动多发性神经病主要累及双侧下肢。大脑和整个脊柱MRI检查在正常范围内。自身免疫检查抗核抗体、抗dsdna、抗smd1、抗组蛋白、抗RibPO、c-ANCA阳性。双侧下肢动静脉彩色多普勒提示踝关节和足部皮下水肿,无深静脉血栓。根据SLICC(系统性狼疮国际合作临床标准)诊断为SLE。因此,这是一个主要表现为血管性多神经病变的SLE病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Atypical Presentation of Systemic Lupus Erythematous with Vasculitic Polyneuropathy
A 22-year-old female patient with Systemic Lupus Erythematous (SLE) without any significant history with no comorbidities presented with complaints of acute onset pain and burning sensation in bilateral lower limbs predominantly involving soles and feet with additional history of hair loss and Malar rash. On evaluation her vitals were stable, pedal edema was present, cardiovascular, respiratory, abdominal system revealed no significant abnormality. Neurological examination revealed absent ankle reflexes bilaterally. Plantars were flexor bilaterally, altered sensation and decreased proprioception and joint sensation bilateral lower limbs. She was evaluated for above mentioned complaints and examination findings. Nerve conduction study revealed severe sensory motor polyneuropathy predominantly involving bilateral lower limbs. MRI Brain and whole spine screening were within normal limits. Autoimmune workup was positive for antinuclear antibodies, anti-dsDNA, anti-SmD1, anti-histone, anti RibPO,c-ANCA. Bilateral lower limb arteriovenous color doppler was suggestive of subcutaneous edema over ankle and foot with no DVT. According to SLICC (systemic lupus international collaborating clinic criteria) was diagnosed with SLE. Hence, this is a case of SLE with primary presentation of vasculitic polyneuropathy.
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