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Tacrolimus toxicity in kidney transplant recipient after wedge liver resection: A case report and review of literature.

World journal of nephrology 2025 Vol.14(4) p. 111723

Naiyarakseree N, Wuttiputhanun T, Townamchai N, Sutherasan M, Avihingsanon Y, Udomkarnjananun S

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[BACKGROUND] Tacrolimus is a key immunosuppressive agent used to prevent allograft rejection in kidney transplant recipients.

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APA Naiyarakseree N, Wuttiputhanun T, et al. (2025). Tacrolimus toxicity in kidney transplant recipient after wedge liver resection: A case report and review of literature.. World journal of nephrology, 14(4), 111723. https://doi.org/10.5527/wjn.v14.i4.111723
MLA Naiyarakseree N, et al.. "Tacrolimus toxicity in kidney transplant recipient after wedge liver resection: A case report and review of literature.." World journal of nephrology, vol. 14, no. 4, 2025, pp. 111723.
PMID 41479815

Abstract

[BACKGROUND] Tacrolimus is a key immunosuppressive agent used to prevent allograft rejection in kidney transplant recipients. Due to its narrow therapeutic index, careful monitoring is essential to avoid adverse effects, particularly neurotoxicity and nephrotoxicity. Hepatic metabolism is an important part of tacrolimus pharmacokinetics. This case report highlights the impact of liver resection on tacrolimus pharmacokinetics in a kidney transplant recipient.

[CASE SUMMARY] A 61-year-old male with end-stage kidney disease underwent a living-unrelated donor kidney transplant at age 46 and has maintained a stable tacrolimus regimen for 15 years. He was later diagnosed with hepatocellular carcinoma and underwent an open wedge liver resection. Despite stable preoperative tacrolimus levels, he developed acute kidney injury and neurotoxicity (manifested as new-onset tremors and headache) postoperatively. Tacrolimus levels rose from 3.4 ng/mL before surgery to 19.5 ng/mL postoperatively, despite no changes in dosage. This increase was most likely due to reduced liver mass and function following resection, in addition to ischemic injury of the remaining liver parenchyma, leading to impaired drug metabolism and acute toxicity. Liver function tests showed transient abnormalities postoperatively, with transaminase levels peaking at 30 times the normal range before gradually returning to normal, coinciding with the decline in tacrolimus levels. The patient's symptoms and acute kidney injury improved as tacrolimus concentration returned to normal.

[CONCLUSION] This is the first reported case of acute tacrolimus neurotoxicity and nephrotoxicity in a kidney transplant recipient following liver resection. It highlights the critical need for vigilant therapeutic drug monitoring of tacrolimus after liver surgery to prevent severe adverse effects.