肾移植受者感染SARS-CoV-2后播散性组织胞浆菌病、肺结核和巨细胞病毒病

Case Reports in Transplantation Pub Date : 2022-08-28 eCollection Date: 2022-01-01 DOI:10.1155/2022/8042168
Carvallo-Venegas Mauricio, Fuentes-López Elsa Angélica, Andrade-Ortega Antonio de Jesús, Torres-Baranda José Rodrigo, Carrasco-Carrizosa Aldo, Cerrillos-Gutierrez José Ignacio, Andrade-Sierra Jorge
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引用次数: 1

摘要

摘要:感染SARS-CoV-2可增加肾移植受者(RTR)发生急性移植物功能障碍(AGD)的风险,同时出现机会性感染的风险也增加。目前对RTR患者SARS-CoV-2感染期间的免疫抑制管理尚无共识。案例演示。来自亲属活体供体的一名35岁男性RTR患者出现SARS-CoV-2感染(2021年1月)。两个月后,尽管改变了免疫抑制方案(他克莫司(TAC)减少50%,随着症状缓解而停用霉酚酸(MMF)),患者仍出现肺结核、呼吸道合胞病毒(RSV)引起的肺炎、巨细胞病毒(CMV)肺炎和组织浆菌病(HP)。治疗开始使用抗结核药物、更昔洛韦、抗生素和两性霉素B脂质体,并暂停使用免疫抑制剂,但患者的演变是灾难性的,结果是致命的。结论:我们建议在covid -19后的RTR中,应逐步恢复免疫抑制方案,同时严格警惕观察高流行的合并感染(TB、HP和CMV)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Disseminated Histoplasmosis, Pulmonary Tuberculosis, and Cytomegalovirus Disease in a Renal Transplant Recipient after Infection with SARS-CoV-2.

Disseminated Histoplasmosis, Pulmonary Tuberculosis, and Cytomegalovirus Disease in a Renal Transplant Recipient after Infection with SARS-CoV-2.

Disseminated Histoplasmosis, Pulmonary Tuberculosis, and Cytomegalovirus Disease in a Renal Transplant Recipient after Infection with SARS-CoV-2.

Disseminated Histoplasmosis, Pulmonary Tuberculosis, and Cytomegalovirus Disease in a Renal Transplant Recipient after Infection with SARS-CoV-2.

Introduction: Infection with SARS-CoV-2 increases the risk of acute graft dysfunction (AGD) in renal transplant recipients (RTR), and the risk of concurrently presenting with opportunistic infections is also increased. There is no current consensus on the management of immunosuppression during SARS-CoV-2 infection in RTR. Case Presentation. A 35-year-old male RTR from a living related donor presented with SARS-CoV-2 infection (January 2021). Two months later, despite alterations to his immunosuppression regimen (tacrolimus (TAC) was reduced by 50%, and the mycophenolic acid (MMF) was suspended with the remission of symptoms), the patient presented with pulmonary tuberculosis, pneumonia due to respiratory syncytial virus (RSV), cytomegalovirus (CMV) pneumonitis, and histoplasmosis (HP). Management was initiated with antituberculosis medications, ganciclovir, antibiotics, and liposomal amphotericin B, and the immunosuppressants were suspended, yet the patient's evolution was catastrophic and the outcome fatal.

Conclusion: We recommend that in RTR post-COVID-19, the immunosuppression regimen should be gradually reinstated along with strict vigilance in observing for highly prevalent coinfections (TB, HP, and CMV).

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