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多发性神经病是原发性系统性淀粉样变性的早期表现。

[Polyneuropathy is an early finding in primary systemic amyloidosis].

作者信息

Romi F, Vedeler C, Tysnes O B, Mørk S, Aarli J A

机构信息

Nevrologisk avdeling, Haukeland Sykehus, Bergen.

出版信息

Tidsskr Nor Laegeforen. 2000 Apr 30;120(11):1291-3.

Abstract

BACKGROUND

Polyneuropathy is associated with several pathological conditions. Amyloidosis is a less common cause of polyneuropathy. Amyloidosis is caused by the accumulation of insoluble protein fibrils (amyloid) in the extracellular matrix. Primary systemic amyloidosis is caused by B-lymphocyte dyscrasia. Polyneuropathy is the first sign of primary systemic amyloidosis in about 20% of the cases, and is characterised by relentless progression, painfulness, and prominent symptoms of autonomic neuropathy.

MATERIAL AND METHODS

We describe three cases of primary systemic amyloidosis that started with polyneuropathy.

RESULTS

The diagnosis of primary systemic amyloidosis is often delayed more than two years after the onset of polyneuropathy. Biopsy of rectum, fat tissue, bone marrow, or peripheral nerve are diagnostic tools.

INTERPRETATION

The survival of non-treated patients is about 18 months after the diagnosis. With chemotherapy the survival is prolonged to approximately 38 months.

摘要

背景

多发性神经病与多种病理状况相关。淀粉样变性是多发性神经病较罕见的病因。淀粉样变性由细胞外基质中不溶性蛋白原纤维(淀粉样蛋白)的积累所致。原发性系统性淀粉样变性由B淋巴细胞异常引起。在约20%的病例中,多发性神经病是原发性系统性淀粉样变性的首发症状,其特征为病情持续进展、疼痛以及明显的自主神经病变症状。

材料与方法

我们描述了3例以多发性神经病起病的原发性系统性淀粉样变性病例。

结果

原发性系统性淀粉样变性的诊断通常在多发性神经病起病后延迟两年以上。直肠、脂肪组织、骨髓或周围神经活检是诊断工具。

解读

未经治疗的患者诊断后生存期约为18个月。化疗可使生存期延长至约38个月。

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