淀粉样变性与腕管综合征:我们能预测发生率吗?

François Saade, Camille Barani, Matthieu Guyard, Matthieu Malatray, Élisabeth Hugon-Vallet, Philippe Schiele
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引用次数: 0

摘要

导言腕管综合征,尤其是双侧腕管综合征,可能与淀粉样蛋白沉积有关,淀粉样蛋白沉积是全身性淀粉样变性的前兆。全身性淀粉样变性会影响多个器官,其中心脏受累的预后最差。诊断往往被延误。目前的治疗方法仅在疾病的早期阶段有效。我们研究的主要目的是评估双侧腕管综合征患者中淀粉样变性的发病率;次要目的是筛查心脏形式:2019年至2023年期间,我们开展了一项单中心前瞻性观察和诊断研究,调查在正中神经开放性神经松解手术中采集的腱鞘样本中淀粉样蛋白沉积的解剖病理。腱鞘活检样本被送往特定实验室进行分析,如果结果呈阳性,则进行分型。如果检测出淀粉样变性,患者将被转诊至专科医生进行具体检查:我们共纳入了 54 名患者,平均年龄为 67 岁(51-89 岁不等):其中男性 16 人,女性 38 人。16例分析结果呈阳性,其中12例为转甲状腺素,4例为非类型:讨论/结论:双侧腕管综合征可预测淀粉样变性。由于手术过程中的滑膜活检简单快捷,因此应在早期发现淀粉样变性。这可能会改变预后,通过筛查和早期特殊治疗提高存活率:证据等级:IV。
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Amyloidosis and carpal tunnel syndrome: can we predict occurrence?

Introduction: Carpal tunnel syndrome, especially when bilateral, may be associated with amyloid deposits, a precursor of systemic amyloidosis. Systemic amyloidosis affects various organs, cardiac involvement having the poorest prognosis. Diagnosis is often delayed. Current treatments are only effective in the early stages of the disease. The primary objective of our study was to evaluate the incidence of amyloidosis in patients with bilateral carpal tunnel syndrome; the secondary aim was to screen for cardiac forms.

Material and methods: Between 2019 and 2023, we conducted a single-center prospective observational and diagnostic study to investigate the anatomical pathology of amyloid deposits in tenosynovial samples taken during open nerve release surgery on the median nerve. The tenosynovial biopsy was sent to a specific laboratory for analysis, and typing if positive. If amyloidosis was detected, the patient was referred to a specialist for a specific work-up.

Results: We included 54 patients, with a mean age of 67 years (range, 51-89 years): 16 men and 38 women. Sixteen analyses were positive, 12 of which were transthyretin and 4 non-typed.

Discussion/conclusion: Bilateral carpal tunnel syndrome was predictive of amyloidosis. As synovial biopsy during surgery is simple and rapid, it should be implemented to identify amyloidosis at an early stage. This could change prognosis, by improving survival through screening and initiation of early specific treatment.

Level of evidence: IV.

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