[关于在日本非流行区早期诊断晚发型遗传性 ATTR 淀粉样变性病的建议]。

Q4 Medicine
Clinical Neurology Pub Date : 2024-10-29 Epub Date: 2024-10-26 DOI:10.5692/clinicalneurol.cn-002002
Keiko Maruyama Saladini, Haruki Koike, Mitsuharu Ueda, Yoshiki Sekijima, Yukio Ando
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引用次数: 0

摘要

非流行地区的晚发型遗传性 ATTR(ATTRv)淀粉样变性由于临床症状多样且无特异性,家族史往往无法确定,因此很多病例需要很长时间才能确诊。近年来,针对 ATTRv 淀粉样变性的疾病改变疗法已经问世,早期诊断的必要性日益凸显。ATTRv 淀粉样变性的诊断通常需要淀粉样沉积的组织学证实,不过淀粉样蛋白的检出率在很大程度上取决于活检医生的经验、知识和技能。将 ATTRv 淀粉样变性作为特发性多发性神经病的一种鉴别疾病非常重要。如果强烈怀疑是 ATTRv 淀粉样变性,那么在进行彻底的鉴别诊断后,在组织学检查前进行 TTR 基因检测是可以接受的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Proposals for the early diagnosis of late-onset hereditary ATTR amyloidosis in ‍nonendemic areas in Japan].

Late-onset hereditary ATTR (ATTRv) amyloidosis in nonendemic areas takes long periods of time to diagnose in many cases because the clinical symptoms are varied and nonspecific with the family history often unidentifiable. In recent years, disease-modifying therapies have been available for ATTRv amyloidosis, and early diagnosis is increasingly needed. The diagnosis of ATTRv amyloidosis usually requires histological confirmation of the amyloid deposition, although the amyloid detection rate largely depends on the experience, knowledge, and skill of the physician who performs the biopsy. It is important to consider ATTRv amyloidosis as a differential disease in idiopathic polyneuropathy. If ATTRv amyloidosis is strongly suspected, it is acceptable to perform TTR genetic testing prior to histological examination after a thorough differential diagnosis has been made.

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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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