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抗组胺药诱发的横纹肌溶解症中肌酸激酶水平大幅升高。

Massively elevated creatine kinase levels in antihistamine-induced rhabdomyolysis.

作者信息

Ramakrishna Karan N, Shah Amish, Martinez-Balzano Carlos D

机构信息

Department of Medicine, State University of New York Upstate Medical UniversitySyracuseNew York.

Division of Pulmonology/Critical Care, Department of Medicine, State University of New York Upstate Medical UniversitySyracuseNew York.

出版信息

Proc (Bayl Univ Med Cent). 2019 Nov 19;33(1):44-46. doi: 10.1080/08998280.2019.1688624. eCollection 2020 Jan.

Abstract

Rhabdomyolysis is the destruction of skeletal muscle tissue with release of intracellular components into the circulation. Elevation of creatine kinase levels in serum is indicative of muscle damage and is associated with acute kidney injury. Antihistamines are a rare cause of nontraumatic rhabdomyolysis. Herein we describe a case of intentional ingestion of diphenhydramine resulting in rhabdomyolysis with subsequent elevation in creatine kinase levels exceeding 2 million IU/L. Aggressive intravenous volume expansion rapidly lowered creatine kinase levels and improved renal function.

摘要

横纹肌溶解症是指骨骼肌组织遭到破坏,细胞内成分释放进入血液循环。血清中肌酸激酶水平升高表明存在肌肉损伤,且与急性肾损伤相关。抗组胺药是导致非创伤性横纹肌溶解症的罕见原因。在此,我们描述一例故意摄入苯海拉明导致横纹肌溶解症的病例,随后肌酸激酶水平升高超过200万国际单位/升。积极的静脉补液迅速降低了肌酸激酶水平并改善了肾功能。

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Massively elevated creatine kinase levels in antihistamine-induced rhabdomyolysis.抗组胺药诱发的横纹肌溶解症中肌酸激酶水平大幅升高。
Proc (Bayl Univ Med Cent). 2019 Nov 19;33(1):44-46. doi: 10.1080/08998280.2019.1688624. eCollection 2020 Jan.
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Antihistamine-induced rhabdomyolysis.抗组胺药引起的横纹肌溶解症。
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本文引用的文献

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Seven-Digit Creatine Kinase in Acute Rhabdomyolysis in a Child.儿童急性横纹肌溶解症中的七位数肌酸激酶
Child Neurol Open. 2017 Jan 4;4:2329048X16684396. doi: 10.1177/2329048X16684396. eCollection 2017 Jan-Dec.
3
Rhabdomyolysis and acute kidney injury.横纹肌溶解症与急性肾损伤。
N Engl J Med. 2009 Jul 2;361(1):62-72. doi: 10.1056/NEJMra0801327.
5
Rhabdomyolysis: an evaluation of 475 hospitalized patients.横纹肌溶解症:对475例住院患者的评估
Medicine (Baltimore). 2005 Nov;84(6):377-385. doi: 10.1097/01.md.0000188565.48918.41.

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