Filosto Massimiliano, Cavallaro Tiziana, Pasolini Giorgio, Broglio Laura, Tentorio Marta, Cotelli Mariasofia, Ferrari Sergio, Padovani Alessandro
Clinical Neurology, Section for Neuromuscular Diseases and Neuropathies, University Hospital Spedali Civili, Brescia, Italy.
J Neurol Sci. 2009 Sep 15;284(1-2):179-81. doi: 10.1016/j.jns.2009.03.027. Epub 2009 Apr 16.
Hypocomplementemic urticarial vasculitis (HUV) is a rare form of cutaneous small-vessel vasculitis characterized by recurrent episodes of urticaria and painful, tender, burning or itchy skin lesions, often associated with extracutaneous involvement but usually with no significant peripheral nerve damage. We describe a patient with an HUV of undetermined cause that developed a progressive multifocal sensory neuropathy whose symptoms were temporarily relieved by intravenous immunoglobulin treatment. Sural nerve biopsy showed asymmetrical multifocal nerve fiber loss and axon degeneration in nerve fascicles, a picture suggestive of ischemic damage as a likely result of a vasculitic process. We point out that an axonal neuropathy may complicate idiopathic HUV and suggest looking for peripheral nerve involvement in HUV patients.
低补体血症性荨麻疹性血管炎(HUV)是一种罕见的皮肤小血管炎,其特征为荨麻疹反复发作以及皮肤出现疼痛、压痛、灼痛或瘙痒性损害,常伴有皮肤外受累,但通常无明显的周围神经损伤。我们描述了一名病因不明的HUV患者,该患者出现了进行性多灶性感觉神经病变,其症状通过静脉注射免疫球蛋白治疗得到了暂时缓解。腓肠神经活检显示神经束中存在不对称的多灶性神经纤维缺失和轴突变性,这一表现提示缺血性损伤可能是血管炎过程的结果。我们指出,轴索性神经病变可能使特发性HUV复杂化,并建议对HUV患者进行周围神经受累情况的检查。