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相似文献

1
[Posterior reversible encephalopathy related to tacrolimus in a liver transplanted HIV patient].[一名肝移植HIV患者中与他克莫司相关的后部可逆性脑病]
Gastroenterol Clin Biol. 2010 Jan;34(1):29-34. doi: 10.1016/j.gcb.2009.07.036. Epub 2009 Sep 24.
2
Reversibility of cytotoxic edema in tacrolimus leukoencephalopathy.他克莫司性白质脑病中细胞毒性水肿的可逆性。
Pediatr Neurol. 2010 Nov;43(5):359-62. doi: 10.1016/j.pediatrneurol.2010.05.021.
3
Tacrolimus leukoencephalopathy--is it posterior reversible encephalopathy syndrome?他克莫司白质脑病——它是后部可逆性脑病综合征吗?
Pediatr Neurol. 2011 Mar;44(3):236; author reply 236. doi: 10.1016/j.pediatrneurol.2010.11.016.
4
Leukoencephalopathy syndrome after living-donor liver transplantation.活体肝移植后的白质脑病综合征
Exp Clin Transplant. 2011 Apr;9(2):139-44.
5
Late onset of tacrolimus-related posterior leukoencephalopathy after living donor liver transplantation.活体肝移植后他克莫司相关迟发性后部白质脑病
Liver Transpl. 2003 Sep;9(9):983-5. doi: 10.1053/jlts.2003.50181.
6
Posterior reversible encephalopathy syndrome in the Intensive Care Unit after liver transplant: a comparison of our experience with the existing literature.肝移植术后重症监护病房中后部可逆性脑病综合征:我们的经验与现有文献的比较。
Minerva Anestesiol. 2012 Jul;78(7):847-50. Epub 2011 Jun 23.
7
Epilepsy after neuroimaging normalization in a woman with tacrolimus-related posterior reversible encephalopathy syndrome.一例他克莫司相关性后部可逆性脑病综合征患者神经影像学正常化后的癫痫发作
Epilepsy Behav. 2010 Apr;17(4):558-60. doi: 10.1016/j.yebeh.2010.01.014. Epub 2010 Feb 18.
8
[Reversible posterior leukoencephalopathy syndrome in patients with immunosuppressive treatment: report of four cases].[免疫抑制治疗患者的可逆性后部白质脑病综合征:4例报告]
Rev Med Chil. 2008 Jan;136(1):93-8. Epub 2008 Apr 30.
9
Alternative tacrolimus and sirolimus regimen associated with rapid resolution of posterior reversible encephalopathy syndrome after lung transplantation.肺移植后,他克莫司与西罗莫司替代方案相关联,可迅速缓解后部可逆性脑病综合征。
Pediatr Neurol. 2014 Mar;50(3):272-5. doi: 10.1016/j.pediatrneurol.2013.11.006. Epub 2013 Nov 16.
10
Severe toxic leukoencephalopathy associated with tacrolimus after living donor liver transplantation.活体肝移植后与他克莫司相关的严重中毒性白质脑病。
Acta Neurol Belg. 2015 Mar;115(1):75-6. doi: 10.1007/s13760-014-0302-2. Epub 2014 May 23.

引用本文的文献

1
Posterior Reversible Encephalopathy Syndrome Induced by an Acute Postinfectious Glomerulonephritis.急性感染后肾小球肾炎诱发的后部可逆性脑病综合征
Int J Pediatr. 2021 Mar 3;2021:8850092. doi: 10.1155/2021/8850092. eCollection 2021.

[一名肝移植HIV患者中与他克莫司相关的后部可逆性脑病]

[Posterior reversible encephalopathy related to tacrolimus in a liver transplanted HIV patient].

作者信息

Courand P-Y, Christin F, Ben Cheikh A, Baillon J-J, Ber C-E, Rimmelé T

机构信息

Département d'anesthésie-réanimation, pavillon P réanimation, hôpital Edouard-Herriot, place d'Arsonval, 69003 Lyon, France.

出版信息

Gastroenterol Clin Biol. 2010 Jan;34(1):29-34. doi: 10.1016/j.gcb.2009.07.036. Epub 2009 Sep 24.

DOI:10.1016/j.gcb.2009.07.036
PMID:19781881
Abstract

Tacrolimus-related posterior reversible leukoencephalopathy (PRLE) is a rare complication which should be recognized by clinicians who regularly use immunosuppressive therapy. We report the case of an HIV-positive, hepatitis C-positive liver transplant patient who presented with this complication. Immunosuppression with tacrolimus was started after postsurgery. On the 20th day, the patient suffered two tonic-clonic convulsive attacks against a background of hypertension. Cerebral magnetic resonance imaging and lumbar puncture led to diagnosis of tacrolimus-related PRLE after eliminating other possible diagnoses. Therapeutic management consisted of withdrawing tacrolimus and initiating treatment with antiepileptogenic and antihypertensive drugs, supplemented with magnesium sulphate. The symptoms regressed in the days following withdrawal of tacrolimus and the majority of lesions on magnetic resonance imaging disappeared within two weeks. The aim of which should be to identify patients at risk of developing this complication. This would enable targeted prevention involving magnesium supplementation, strict control of blood pressure and serial monitoring of tacrolimus blood concentrations.

摘要

他克莫司相关的后部可逆性白质脑病(PRLE)是一种罕见的并发症,经常使用免疫抑制疗法的临床医生应认识到这一点。我们报告了一例出现这种并发症的HIV阳性、丙型肝炎阳性的肝移植患者。术后开始使用他克莫司进行免疫抑制治疗。在第20天,患者在高血压背景下发生了两次强直阵挛性惊厥发作。在排除其他可能的诊断后,通过脑磁共振成像和腰椎穿刺诊断为他克莫司相关的PRLE。治疗措施包括停用他克莫司,并开始使用抗癫痫和抗高血压药物进行治疗,辅以硫酸镁。停用他克莫司后的几天内症状消退,磁共振成像上的大多数病变在两周内消失。其目的应该是识别有发生这种并发症风险的患者。这将有助于进行有针对性的预防,包括补充镁、严格控制血压以及连续监测他克莫司血药浓度。