Suppr超能文献

伴有颞动脉累及的 AL 淀粉样变性模拟巨细胞动脉炎。

AL amyloidosis with temporal artery involvement simulates giant-cell arteritis.

机构信息

Department of Internal Medicine, CHU de Caen, 14000 Caen, France.

出版信息

Joint Bone Spine. 2012 Mar;79(2):195-7. doi: 10.1016/j.jbspin.2011.09.007. Epub 2011 Dec 28.

Abstract

Light-chain (AL) amyloidosis may present with features suggesting vasculitis, including giant-cell arteritis (GCA). We describe a case of an 80-year-old man, who initially presented with bilateral jaw claudication, bi-temporal headache and arthralgia, however a temporal-artery biopsy then revealed AL amyloidosis. A diagnosis of AL amyloidosis complicating multiple myelome simulates GCA and polymyalgia rheumatica was established. The patient was successfully treated with melphalan and dexamethasone: the free kappa light chains decreased, the patient's jaw claudication and headache disappeared. Then we discuss similarities between GCA and AL amyloidosis and potential confusion in diagnosis. We suggest that, in patients with clinical features of GCA without any temporal-artery typical findings, specimens are stained with Congo red, which then results in a different diagnosis and treatment.

摘要

轻链(AL)淀粉样变性症可能表现出类似于血管炎的特征,包括巨细胞动脉炎(GCA)。我们描述了一例 80 岁男性患者,他最初表现为双侧下颌跛行、双颞部头痛和关节痛,但颞动脉活检后发现为 AL 淀粉样变性症。AL 淀粉样变性症并发多发性骨髓瘤模拟 GCA 和风湿性多肌痛的诊断成立。该患者成功接受了美法仑和地塞米松治疗:游离 κ 轻链减少,患者的下颌跛行和头痛消失。然后我们讨论了 GCA 和 AL 淀粉样变性症之间的相似之处以及诊断方面的潜在混淆。我们建议,对于具有 GCA 临床特征但无任何颞动脉典型表现的患者,应使用刚果红染色标本,从而得出不同的诊断和治疗方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验