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肝移植后他克莫司诱发的腹水

Tacrolimus-induced Ascites after Liver Transplant.

作者信息

Hosseini M, Aliakbarian M, Akhavan-Rezayat K, Shadkam O, Milani S

机构信息

Department of Internal Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Surgical Oncology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

Int J Organ Transplant Med. 2018;9(2):102-104. Epub 2018 May 1.

PMID:30834095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6390981/
Abstract

Massive post-transplantation ascites is a rare but serious condition following liver transplantation. Although, many etiologies are suggested as the cause of this complication, in some cases the definitive etiology remains unknown. Drug-induced post-transplantation ascites is one of the possible etiologies. In this study we present a case of ascites caused by tacrolimus in the post-liver transplantation period. A 49-year-old man with hepatitis B virus cirrhosis underwent liver transplantation and received tacrolimus, mycophenolate and prednisolone, as the immunosuppressive regimen. Progressive ascites developed after 10 days, in spite of a normal liver function. Various studies, including liver biopsy, were performed but we could not find any etiology for this complication. The tacrolimus was switched to rapamune. Ascites was completely disappeared and up to the last follow-up visit, the patient remained asymptomatic for more than two years. We concluded that after ruling out other etiologies, tacrolimus as a rare cause of post-transplantation ascites should be taken into account. The treatment is discontinuation of the drug.

摘要

肝移植后大量腹水是肝移植后一种罕见但严重的病症。尽管有许多病因被认为是这种并发症的原因,但在某些情况下,确切病因仍不明。药物性肝移植后腹水是可能的病因之一。在本研究中,我们报告一例肝移植术后由他克莫司引起腹水的病例。一名49岁的乙肝肝硬化男性接受了肝移植,并接受他克莫司、霉酚酸酯和泼尼松龙作为免疫抑制方案。尽管肝功能正常,但10天后出现进行性腹水。进行了包括肝活检在内的各种检查,但我们未能找到该并发症的任何病因。将他克莫司换为雷帕鸣。腹水完全消失,直至最后一次随访,患者在两年多时间里一直无症状。我们得出结论,在排除其他病因后,应考虑他克莫司作为肝移植后腹水的罕见病因。治疗方法是停用该药物。

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Tacrolimus-induced Ascites after Liver Transplant.肝移植后他克莫司诱发的腹水
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引用本文的文献

1
Hepatic sinusoidal obstruction syndrome induced by tacrolimus following liver transplantation: Three case reports.肝移植后他克莫司诱发的肝窦阻塞综合征:三例报告
World J Clin Cases. 2022 Dec 26;10(36):13408-13417. doi: 10.12998/wjcc.v10.i36.13408.
2
Approach to persistent ascites after liver transplantation.肝移植后持续性腹水的处理方法
World J Hepatol. 2022 Sep 27;14(9):1739-1746. doi: 10.4254/wjh.v14.i9.1739.

本文引用的文献

1
Tacrolimus as a Rare Cause of Pericardial Effusion in a Renal Transplant Recipient.他克莫司作为肾移植受者心包积液的罕见病因。
Heart Views. 2017 Oct-Dec;18(4):145-148. doi: 10.4103/HEARTVIEWS.HEARTVIEWS_6_17.
2
Reversible sinusoidal obstruction syndrome associated with tacrolimus following liver transplantation.肝移植后与他克莫司相关的可逆性窦性阻塞综合征
World J Gastroenterol. 2015 May 28;21(20):6422-6. doi: 10.3748/wjg.v21.i20.6422.
3
The calcineurin inhibitor tacrolimus activates the renal sodium chloride cotransporter to cause hypertension.钙调磷酸酶抑制剂他克莫司激活肾脏钠氯共转运蛋白,导致高血压。
Nat Med. 2011 Oct 2;17(10):1304-9. doi: 10.1038/nm.2497.
4
Intractable ascites without mechanical vascular obstruction after orthotopic liver transplantation: etiology and clinical outcome of sinusoidal obstruction syndrome.原位肝移植后无机械性血管阻塞的难治性腹水:窦阻塞综合征的病因和临床转归。
Clin Transplant. 2010 Jan-Feb;24(1):139-48. doi: 10.1111/j.1399-0012.2009.00971.x. Epub 2009 Feb 12.
5
A retrospective study of conversion from tacrolimus-based to sirolimus-based immunosuppression in orthotopic liver transplant recipients.一项关于原位肝移植受者从基于他克莫司的免疫抑制转换为基于西罗莫司的免疫抑制的回顾性研究。
Exp Clin Transplant. 2008 Jun;6(2):113-7.
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Transpl Int. 2005 Oct;18(10):1215-7. doi: 10.1111/j.1432-2277.2005.00204.x.
7
AUC-guided dosing of tacrolimus prevents progressive systemic overexposure in renal transplant recipients.以AUC为指导的他克莫司给药可防止肾移植受者全身性暴露过度进展。
Kidney Int. 2005 Jun;67(6):2440-7. doi: 10.1111/j.1523-1755.2005.00352.x.
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Sirolimus in liver transplantation.
Transplant Proc. 2003 May;35(3 Suppl):193S-200S. doi: 10.1016/s0041-1345(03)00234-3.
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Ascites.
Clin Liver Dis. 2000 Feb;4(1):151-68, vii. doi: 10.1016/s1089-3261(05)70101-x.
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Ascites after liver transplantation.肝移植后的腹水
Liver Transpl. 2000 Mar;6(2):157-62. doi: 10.1002/lt.500060219.