[一名50岁的男子,下肢逐渐衰弱]。

IF 0.4 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Brynhildur Thors, Bjarni Gudmundsson
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引用次数: 0

摘要

Lambert-Eaton肌肉无力综合征(LEMS)是一种罕见的神经系统疾病,由自身免疫抗体攻击突触前神经肌肉接头引起,在某些情况下由潜在的癌症引起。主要的临床发现是四肢无力的波动,三重症状可以帮助医生怀疑这种疾病。诊断的关键是在这组疾病中发现的电生理异常。症状和/或免疫抑制疗法的治疗以及可能的恶性肿瘤的检查都很重要。本文对这种罕见疾病的临床特点、诊断和治疗进行了阐述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A 50 year old man with progressive weakness in lower limbs].

Lambert-Eaton Myasthenic Syndrome (LEMS) is a rare neurological disorder caused by autoimmune antibodies attacking the presynaptic neuromuscular junction, in some cases caused by underlying cancer. The main clinical finding is fluctuating weakness of the extremities and a triad of symtoms can help physicians suspect the disease. A key to the diagnosis are the electrophysiological abnormalities seen in this group of diseases. Treatment with symtomatic and/or immunosuppressive therapy is important as well as a workup for possible malignancy. This article identifies the clinical features, diagnosis and treatment of this uncommon disease.

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来源期刊
Laeknabladid
Laeknabladid MEDICINE, GENERAL & INTERNAL-
CiteScore
0.50
自引率
25.00%
发文量
63
审稿时长
>12 weeks
期刊介绍: Læknablaðið er fræðirit sem birtir vísinda og yfirlitsgreinar og annað efni sem byggir á rannsóknum innan læknisfræði eða skyldra greina. Læknablaðið er gefið út af Læknafélagi Íslands. Blaðið er sent til allra félagsmanna. Það var fyrst gefið út árið 1904 en hefur komið samfellt út frá árinu 1915. Blaðið kemur út 11 sinnum á ári og er prentað í 2000 eintökum. Allt efni Læknablaðsins frá árinu 2000 er aðgengilegt á heimasíðu blaðsins á laeknabladid.is og er aðgangur endurgjaldslaus og öllum opinn.
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