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遗传性 ATTR V30M 淀粉样变性伴腕管综合征患者腕横韧带中的淀粉样蛋白检测。

Amyloid detection in the transverse carpal ligament of patients with hereditary ATTR V30M amyloidosis and carpal tunnel syndrome.

机构信息

a Neurology Department , Centro Hospitalar do Porto - Hospital de Santo António , Porto , Portugal.

b Neuropathology Unit , Centro Hospitalar do Porto - Hospital de Santo António , Porto , Portugal.

出版信息

Amyloid. 2017 Jun;24(2):73-77. doi: 10.1080/13506129.2017.1313222. Epub 2017 Apr 16.

DOI:10.1080/13506129.2017.1313222
PMID:28413892
Abstract

INTRODUCTION

Carpal tunnel syndrome (CTS) is a nonspecific manifestation of hereditary ATTR amyloidosis (ATTRm). Amyloid deposition of wild-type TTR (WT-ATTR) has been found in transverse carpal ligament (TCL) in idiopathic CTS. We retrospectively studied a group of patients with ATTRm and CTS submitted to carpal tunnel release surgery (CTRS).

METHODS

From the nerve conduction studies performed in our Clinical Unit dedicated to hereditary amyloidosis between July 2009 and October 2013, we selected patients who fulfilled neurophysiological criteria for CTS, had been submitted to CTRS and whose TCL was available for pathology. Clinical registries were reviewed and amyloid detection in the ligaments was performed using Congo-red staining.

RESULTS

We included 16 patients: three males (18.8%), mean age = 46.1 years old, all with V30M mutation. At the time of surgery, four patients were considered asymptomatic and 12 symptomatic carriers, five of them late-onset ATTRm (onset age >50 years old). In all but one patient, the CTS preceded the polyneuropathy. Amyloid detection in the TCL was positive in 14 patients (87.5%).

DISCUSSION/CONCLUSIONS: In most patients, CTS preceded or was contemporary to the polyneuropathy and amyloid detection in TCL was positive. The detection of amyloid in TCL may add specificity to CTS as an early manifestation of the disease but more studies are needed.

摘要

简介

腕管综合征(CTS)是遗传性ATTR 淀粉样变性(ATTRm)的非特异性表现。在特发性 CTS 中,已发现野生型 TTR(WT-ATTR)的淀粉样蛋白沉积在横腕韧带(TCL)中。我们回顾性研究了一组接受腕管松解术(CTRS)的 ATTRm 和 CTS 患者。

方法

从 2009 年 7 月至 2013 年 10 月在我们专门用于遗传性淀粉样变性的神经传导研究中,我们选择了符合 CTS 神经生理学标准、已接受 CTRS 治疗且 TCL 可用于病理检查的患者。回顾临床记录,并使用刚果红染色检测韧带中的淀粉样蛋白。

结果

我们纳入了 16 名患者:3 名男性(18.8%),平均年龄为 46.1 岁,均携带 V30M 突变。在手术时,4 名患者无症状,12 名患者为有症状的携带者,其中 5 名患者为迟发性 ATTRm(发病年龄>50 岁)。除了一名患者外,所有患者的 CTS 均先于多发性神经病。14 名患者(87.5%)的 TCL 中检测到淀粉样蛋白。

讨论/结论:在大多数患者中,CTS 先于或与多发性神经病同时发生,并且 TCL 中检测到淀粉样蛋白呈阳性。在 TCL 中检测到淀粉样蛋白可能会增加 CTS 作为疾病早期表现的特异性,但需要更多的研究。

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