Suppr超能文献

[临床神经病学中的肌肉肥大(作者译)]

[Muscular hypertrophy in clinical neurology (author's transl)].

作者信息

Verret J M, Lapresle J

出版信息

Acta Neurol Belg. 1981 Jan-Feb;81(1):33-51.

PMID:7223356
Abstract

The authors begin this general review with the pseudohypertrophies due either to an underlying extramuscular process, or to a focal lesion within the muscle, or else to miscellaneous interstitial infiltrates such as those found in cysticercosis, sarcoidosis, amylosis. True hypertrophy is most often observed in the course of muscular dystrophy. It is an usual finding in myopathies, and the prominent symptom of Thomsen disease ; it is the only symptom of hypertrophia musculorum vera and masseters hypertrophy ; it is associated with a peculiar deficit in the "Hereditary Distal Myopathy with Onset in Infancy"; it is a classical symptom of some endocrine myopathies (hypothyroidism and acromegaly). Paradoxically, true hypertrophy may, though very rarely, be encountered in the course of nervous system diseases, most often of the neuritic type : sciatica, hypertrophic neuritis, progressive spinal muscular atrophy. The mechanism of this very unusual muscular reaction remains unknown.

摘要

作者在这篇综述开篇讨论了假性肥大,其病因要么是潜在的肌外病变,要么是肌肉内的局灶性病变,要么是诸如囊尾蚴病、结节病、淀粉样变性等各种间质浸润。真性肥大最常见于肌营养不良病程中。这在肌病中是常见表现,是汤姆森病的突出症状;是真性进行性肌肥大和咬肌肥大的唯一症状;与“婴儿期起病的遗传性远端肌病”中的特殊缺陷相关;是一些内分泌肌病(甲状腺功能减退和肢端肥大症)的典型症状。矛盾的是,真性肥大虽然极为罕见,但可能出现在神经系统疾病病程中,最常见于神经炎类型:坐骨神经痛、肥大性神经炎、进行性脊髓性肌萎缩。这种非常不寻常的肌肉反应机制尚不清楚。

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