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迟发性转甲状腺素蛋白淀粉样变神经病的表型:一项诊断挑战。

Phenotypes of Late-Onset Transthyretin Amyloid Neuropathy: A Diagnostic Challenge.

作者信息

Živković Saša A, Mnatsakanova Diana, Lacomis David

机构信息

Department of Neurology, UPMC, Pittsburgh, PA.

Department of Neurology and Rehabilitation, University of Illinois, Chicago, IL.

出版信息

J Clin Neuromuscul Dis. 2019 Sep;21(1):1-6. doi: 10.1097/CND.0000000000000252.

Abstract

Hereditary transthyretin amyloidosis (hATTR) is a rare cause of severe neuropathy, typically with progressive sensorimotor and autonomic manifestations. The clinical course is marked by progressive worsening with typical survival of 7-11 years following the onset of symptoms. The phenotype may resemble other types of neuropathy, and dysautonomia may be absent at onset delaying the diagnosis. Two medications were recently approved for treatment of hATTR neuropathy in the United States and more may follow. Three major phenotypes of hATTR include neuropathic, cardiac, and mixed. Diagnostic clues include "red-flag" symptoms reflecting typical multisystem involvement, often presenting with cardiomyopathy, gastrointestinal dysmotility, or kidney insufficiency. We present a case series of 4 patients with late-onset hATTR neuropathy who were initially diagnosed with vasculitic neuropathy and chronic inflammatory demyelinating polyneuropathy to illustrate diagnostic challenges encountered with hATTR. Early diagnosis is even more urgent now given the availability of disease modifying treatments.

摘要

遗传性转甲状腺素蛋白淀粉样变性(hATTR)是严重神经病变的罕见病因,通常伴有进行性感觉运动和自主神经表现。临床病程以进行性恶化为特征,症状出现后典型生存期为7至11年。其表型可能类似于其他类型的神经病变,且发病时可能无自主神经功能障碍,从而延迟诊断。最近美国有两种药物被批准用于治疗hATTR神经病变,可能还会有更多药物获批。hATTR的三种主要表型包括神经病变型、心脏型和混合型。诊断线索包括反映典型多系统受累的“警示”症状,常表现为心肌病、胃肠动力障碍或肾功能不全。我们报告了一组4例迟发性hATTR神经病变患者的病例系列,这些患者最初被诊断为血管炎性神经病变和慢性炎症性脱髓鞘性多发性神经病变,以说明hATTR所面临的诊断挑战。鉴于有改善病情的治疗方法,早期诊断现在更加紧迫。

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