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首页> 外文期刊>Arquivos de Neuro-Psiquiatria >Axoval neuropathy as initial manifestation of primary amyloidosis: report of a case submitted to bone marrow transplantation
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Axoval neuropathy as initial manifestation of primary amyloidosis: report of a case submitted to bone marrow transplantation

机译:腋窝神经病为原发性淀粉样变性病的初始表现:提交骨髓移植的病例报告

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摘要

Amyloidosis is a syndrome characterized by deposition of a highly insoluble protein material in the extracellular space that may affect several organs. It may be generalized and idiopathic (primary amyloidosis). We describe the case of a 48 years-old woman with axonal neuropathy associated with proteinuria, whose final investigation resulted in diagnosis of primary amyloidosis (AL). She was submitted to autologous bone marrow transplantation. We discuss some aspects related to diagnosis of neuropathy and current treatment of AL.
机译:淀粉样变性病是一种综合征,其特征是高度不溶的蛋白质物质沉积在细胞外空间中,可能影响多个器官。它可能是全身性和特发性的(原发性淀粉样变性)。我们描述了一个患有蛋白尿相关的轴索神经病的48岁女性的病例,其最终调查结果诊断为原发性淀粉样变性病(AL)。她接受了自体骨髓移植。我们讨论与神经病变的诊断和AL的当前治疗有关的一些方面。

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