肝移植受者中与钙神经蛋白抑制剂相关的后可逆性脑病综合征:三份病例报告和文献综述。

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY
Yu Gong
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引用次数: 0

摘要

背景:后可逆性脑病综合征(PRES)以急性神经功能衰退和 T2-流体衰减反转恢复磁共振成像(MRI)显示的广泛白质病变为特征,越来越多地与钙神经蛋白抑制剂(CNI)相关的神经毒性联系在一起。及时诊断至关重要,因为早期干预,包括调整或停止 CNI 治疗、严格控制血压、皮质类固醇治疗和支持性护理,可显著改善患者的预后。临床上对 CNI 相关 PRES 的认识不断提高,这突出表明了在出现急性神经症状的患者中识别和处理这种疾病的重要性。第一个病例是一名 60 岁的女性,她在术后第 9 天(POD)出现癫痫发作、失语和偏瘫,核磁共振成像显示缺血灶,随后出现广泛的白质病变。更换他克莫司后,她的症状有所改善,随访三年后也未发现明显的磁共振成像异常。第二个病例涉及一名患有自身免疫性肝炎的 54 岁女性,她在 POD24 出现头痛、癫痫发作,并在核磁共振成像中出现广泛的白质脱髓鞘。在改用雷帕霉素并开始使用皮质类固醇后,她的症状得到缓解,并于 POD95 出院。第三个病例是一名患有肝细胞癌的 60 岁女性患者,她在 POD11 出现脑磁共振成像异常,证明她患上了 PRES。转用雷帕霉素和皮质类固醇治疗后,她完全康复,并于 POD22 出院。这些病例突出表明,早期诊断、调整 CNI 和严格管理对于改善患有 CNI 相关 PRES 的肝移植受者的预后至关重要:结论:临床表现结合特征性磁共振成像结果是诊断器官移植受者PRES的关键。然而,当标准治疗无效或磁共振成像结果不典型时,应考虑其他诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Calcineurin inhibitors-related posterior reversible encephalopathy syndrome in liver transplant recipients: Three case reports and review of literature.

Background: Posterior reversible encephalopathy syndrome (PRES), characterized by acute neurological deterioration and extensive white matter lesions on T2-fluid attenuated inversion recovery magnetic resonance imaging (MRI), is increasingly associated with calcineurin inhibitors (CNI)-related neurotoxicity. Prompt diagnosis is crucial, as early intervention, including the modification or discontinuation of CNI therapy, strict blood pressure management, corticosteroid treatment, and supportive care can significantly improve patient outcomes and prognosis. The growing clinical recognition of CNI-related PRES underscores the importance of identifying and managing this condition in patients presenting with acute neurological symptoms.

Case summary: This report describes three cases of liver transplant recipients who developed PRES. The first case involves a 60-year-old woman who experienced seizures, aphasia, and hemiplegia on postoperative day (POD) 9, with MRI revealing ischemic foci followed by extensive white matter lesions. After replacing tacrolimus, her symptoms improved, and no significant MRI abnormalities were observed after three years of follow-up. The second case concerns a 54-year-old woman with autoimmune hepatitis who developed headaches, seizures, and extensive white matter demyelination on MRI on POD24. Following the switch to rapamycin and the initiation of corticosteroids, her symptoms resolved, and she was discharged on POD95. The third case details a 60-year-old woman with hepatocellular carcinoma who developed PRES, evidenced by brain MRI abnormalities on POD11. Transitioning to rapamycin and corticosteroid therapy led to her full recovery, and she was discharged on POD22. These cases highlight the critical importance of early diagnosis, CNI modification, and stringent management in improving outcomes for liver transplant recipients with CNI-related PRES.

Conclusion: Clinical manifestations, combined with characteristic MRI findings, are crucial in diagnosing PRES among organ transplant recipients. However, when standard treatments are ineffective or MRI results are atypical, alternative diagnoses should be taken into considered.

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来源期刊
World Journal of Hepatology
World Journal of Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.10
自引率
4.20%
发文量
172
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