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手外科医生和淀粉样变性病专家警告:以正中神经分支为病因的转甲状腺素蛋白相关性淀粉样变性病导致双侧腕管综合征。病例报告及文献综述。

Hand surgeons and amyloidosis specialists warning: transthyretin-associated amyloidosis with bifid median nerve as a cause of bilateral carpal tunnel syndrome. A case report and literature review.

作者信息

Triguero Andreu, González-Costello José, López-Marne Silvia, Llop Alfred, Pané Maria, Yun Sergi

机构信息

Department of Orthopaedic Surgery and Traumatology, Bellvitge University Hospital, L'Hospitalet de Llobregat, Barcelona, Spain.

Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.

出版信息

Eur J Orthop Surg Traumatol. 2022 Apr;32(3):575-581. doi: 10.1007/s00590-021-03004-1. Epub 2021 May 29.

Abstract

INTRODUCTION

Approximately 75% of patients with carpal tunnel syndrome (CTS) are diagnosed as idiopathic. Despite this, the presence of an underlying cause such as an anatomical variant or a systemic disease must always be suspected, especially in cases of bilateral presentation without an obvious cause, recurrence or complications. The anatomical variant known as the bifid median nerve (BMN) is a very rare abnormality that can occasionally lead to CTS. On the other hands, transthyretin-associated amyloidosis (ATTR) is one of the possible causes of bilateral CTS. We report a case where these two very rare pathologies converge as the cause of bilateral CTS and a review of the literature.

CASE REPORT

We report a 71-year-old male with prior history of lumbar canal stenosis, bilateral trigger finger, rupture of the supraspinatus muscle tendon and of the long portion of the right biceps brachial. He also had 8-year-old bilateral CTS that recurred after CTS surgery. He was surgically re-intervened and was diagnosed incidentally with BMN and an ultrasound of the other hands also showed BMN. Because of all the prior musculoskeletal history, a biopsy of the transverse carpal ligament was taken showing ATTR deposits that led to the diagnosis of cardiac ATTR wild type.

CONCLUSIONS

This case highlights the natural history of the multiple musculoskeletal manifestations related to ATTR and the importance of performing intraoperative biopsies in patients with CTS surgery as this can lead to early diagnosis of cardiac ATTR.

摘要

引言

大约75%的腕管综合征(CTS)患者被诊断为特发性。尽管如此,必须始终怀疑存在潜在病因,如解剖变异或全身性疾病,特别是在双侧发病且无明显病因、复发或并发症的情况下。被称为双叉正中神经(BMN)的解剖变异是一种非常罕见的异常情况,偶尔可导致CTS。另一方面,转甲状腺素蛋白相关淀粉样变性(ATTR)是双侧CTS的可能病因之一。我们报告一例这两种非常罕见的病理情况共同导致双侧CTS的病例,并对文献进行综述。

病例报告

我们报告一名71岁男性,既往有腰椎管狭窄、双侧扳机指、冈上肌腱和右肱二头肌长头肌腱断裂病史。他还患有8年的双侧CTS,在CTS手术后复发。他接受了再次手术干预,术中偶然诊断为BMN,对其双手进行超声检查也显示存在BMN。鉴于所有既往肌肉骨骼病史,对腕横韧带进行活检,发现ATTR沉积,从而诊断为心脏野生型ATTR。

结论

本病例突出了与ATTR相关的多种肌肉骨骼表现的自然病程,以及在CTS手术患者中进行术中活检的重要性,因为这可导致心脏ATTR的早期诊断。

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