Tacrolimus-induced neurotoxicity from bipolar disorder to status epilepticus under the therapeutic serum level: a case report

Abstract Background Tacrolimus is a macrolide immunosuppressant widely used to prevent rejection after solid organ transplantation. In general, adverse events of tacrolimus occur more often as the concentration of tacrolimus in the blood increases. We report the case of a 39-year-old man who develop...

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Autores principales: Bora Jin, Ga Yeon Kim, Sang-Myung Cheon
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Publicado: BMC 2021
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Acceso en línea:https://doaj.org/article/535c7bd1cae9452081f5b75b8174a32e
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spelling oai:doaj.org-article:535c7bd1cae9452081f5b75b8174a32e2021-11-21T12:09:35ZTacrolimus-induced neurotoxicity from bipolar disorder to status epilepticus under the therapeutic serum level: a case report10.1186/s12883-021-02479-z1471-2377https://doaj.org/article/535c7bd1cae9452081f5b75b8174a32e2021-11-01T00:00:00Zhttps://doi.org/10.1186/s12883-021-02479-zhttps://doaj.org/toc/1471-2377Abstract Background Tacrolimus is a macrolide immunosuppressant widely used to prevent rejection after solid organ transplantation. In general, adverse events of tacrolimus occur more often as the concentration of tacrolimus in the blood increases. We report the case of a 39-year-old man who developed a variety of adverse events despite in the therapeutic level of tacrolimus in the blood. Case presentation A 39-year-old man underwent liver transplantation for liver cirrhosis due to alcoholic liver disease. The postoperative immunosuppressant consisted of tacrolimus (5 mg) and mycophenolate (500 mg) twice daily. Five months after taking tacrolimus, he presented with talkativeness, which gradually worsened. Brain magnetic resonance imaging performed 10 months after tacrolimus administration revealed a hyperintense lesion affecting the middle of the pontine tegmentum on T2WI. The blood concentration of tacrolimus was 7.2 ng/mL (therapeutic range 5–20 ng/mL). After 21 months, he exhibited postural tremor in both the hands. Twenty-four months after taking tacrolimus, he showed drowsy mentality, intention tremor, and dysdiadochokinesia. Electroencephalography presented generalized high-voltage rhythmic delta waves; therefore, tacrolimus was discontinued in suspicion of tacrolimus-induced neurotoxicity, and anticonvulsive treatment was started. The level of consciousness gradually improved, and the patient was able to walk independently with mild ataxia. Conclusion This case shows that tacrolimus-induced neurotoxicity can occur even at normal concentrations. Therefore, if a patient taking tacrolimus exhibits psychiatric or neurologic symptoms, neurotoxicity should be considered even when the blood tacrolimus is within the therapeutic range.Bora JinGa Yeon KimSang-Myung CheonBMCarticleTacrolimusNeurotoxicityBipolar disorderAtaxiaStatus epilepticusNeurology. Diseases of the nervous systemRC346-429ENBMC Neurology, Vol 21, Iss 1, Pp 1-5 (2021)
institution DOAJ
collection DOAJ
language EN
topic Tacrolimus
Neurotoxicity
Bipolar disorder
Ataxia
Status epilepticus
Neurology. Diseases of the nervous system
RC346-429
spellingShingle Tacrolimus
Neurotoxicity
Bipolar disorder
Ataxia
Status epilepticus
Neurology. Diseases of the nervous system
RC346-429
Bora Jin
Ga Yeon Kim
Sang-Myung Cheon
Tacrolimus-induced neurotoxicity from bipolar disorder to status epilepticus under the therapeutic serum level: a case report
description Abstract Background Tacrolimus is a macrolide immunosuppressant widely used to prevent rejection after solid organ transplantation. In general, adverse events of tacrolimus occur more often as the concentration of tacrolimus in the blood increases. We report the case of a 39-year-old man who developed a variety of adverse events despite in the therapeutic level of tacrolimus in the blood. Case presentation A 39-year-old man underwent liver transplantation for liver cirrhosis due to alcoholic liver disease. The postoperative immunosuppressant consisted of tacrolimus (5 mg) and mycophenolate (500 mg) twice daily. Five months after taking tacrolimus, he presented with talkativeness, which gradually worsened. Brain magnetic resonance imaging performed 10 months after tacrolimus administration revealed a hyperintense lesion affecting the middle of the pontine tegmentum on T2WI. The blood concentration of tacrolimus was 7.2 ng/mL (therapeutic range 5–20 ng/mL). After 21 months, he exhibited postural tremor in both the hands. Twenty-four months after taking tacrolimus, he showed drowsy mentality, intention tremor, and dysdiadochokinesia. Electroencephalography presented generalized high-voltage rhythmic delta waves; therefore, tacrolimus was discontinued in suspicion of tacrolimus-induced neurotoxicity, and anticonvulsive treatment was started. The level of consciousness gradually improved, and the patient was able to walk independently with mild ataxia. Conclusion This case shows that tacrolimus-induced neurotoxicity can occur even at normal concentrations. Therefore, if a patient taking tacrolimus exhibits psychiatric or neurologic symptoms, neurotoxicity should be considered even when the blood tacrolimus is within the therapeutic range.
format article
author Bora Jin
Ga Yeon Kim
Sang-Myung Cheon
author_facet Bora Jin
Ga Yeon Kim
Sang-Myung Cheon
author_sort Bora Jin
title Tacrolimus-induced neurotoxicity from bipolar disorder to status epilepticus under the therapeutic serum level: a case report
title_short Tacrolimus-induced neurotoxicity from bipolar disorder to status epilepticus under the therapeutic serum level: a case report
title_full Tacrolimus-induced neurotoxicity from bipolar disorder to status epilepticus under the therapeutic serum level: a case report
title_fullStr Tacrolimus-induced neurotoxicity from bipolar disorder to status epilepticus under the therapeutic serum level: a case report
title_full_unstemmed Tacrolimus-induced neurotoxicity from bipolar disorder to status epilepticus under the therapeutic serum level: a case report
title_sort tacrolimus-induced neurotoxicity from bipolar disorder to status epilepticus under the therapeutic serum level: a case report
publisher BMC
publishDate 2021
url https://doaj.org/article/535c7bd1cae9452081f5b75b8174a32e
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AT gayeonkim tacrolimusinducedneurotoxicityfrombipolardisordertostatusepilepticusunderthetherapeuticserumlevelacasereport
AT sangmyungcheon tacrolimusinducedneurotoxicityfrombipolardisordertostatusepilepticusunderthetherapeuticserumlevelacasereport
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