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横纹肌溶解症:文献综述

Rhabdomyolysis: a review of the literature.

作者信息

Poels P J, Gabreëls F J

机构信息

Institute of Neurology, University Hospital, Nijmegen, The Netherlands.

出版信息

Clin Neurol Neurosurg. 1993 Sep;95(3):175-92. doi: 10.1016/0303-8467(93)90122-w.

Abstract

Rhabdomyolysis (lysis of skeletal muscle cells) is a potentially lethal syndrome with a broad spectrum of clinical and biochemical findings. Myalgia, pigmenturia and elevated activity of serum creatine kinase are the common features. Fulminant rhabdomyolysis may be associated with severe metabolic disturbances and involvement of other organ systems. Cardiac arrest, compartment syndrome and acute renal failure are the major complications. The extent of the life-threatening complications of rhabdomyolysis strongly depends on early diagnosis and adequate therapy. As the repair mechanism of striated muscle functions very well, the prognosis of adequately treated rhabdomyolysis is excellent. This article reviews the present state of knowledge of clinical and biochemical diagnosis of rhabdomyolysis, the pathophysiologic background, the classification and the etiological provocative factors.

摘要

横纹肌溶解症(骨骼肌细胞溶解)是一种具有广泛临床和生化表现的潜在致命综合征。肌痛、色素尿和血清肌酸激酶活性升高是其常见特征。暴发性横纹肌溶解症可能与严重的代谢紊乱及其他器官系统受累有关。心脏骤停、骨筋膜室综合征和急性肾衰竭是主要并发症。横纹肌溶解症危及生命的并发症的严重程度很大程度上取决于早期诊断和适当治疗。由于横纹肌的修复机制运行良好,经过适当治疗的横纹肌溶解症预后良好。本文综述了横纹肌溶解症临床和生化诊断、病理生理背景、分类及病因诱发因素的当前知识状况。

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