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系统性淀粉样变性的肾移植。

Kidney Transplantation in Systemic Amyloidosis.

机构信息

Renal Section, Department of Medicine, Boston University School of Medicine, Boston, MA.

Amyloidosis Center, Boston University School of Medicine, Boston, MA.

出版信息

Transplantation. 2020 Oct;104(10):2035-2047. doi: 10.1097/TP.0000000000003170.

DOI:10.1097/TP.0000000000003170
PMID:32053574
Abstract

The present review discusses current developments and outcomes of renal transplantation in systemic amyloidosis. Amyloidosis can wreak havoc on the architecture and functioning of the kidneys, leading to end-stage renal disease. In recent years, the available treatments, especially for light-chain amyloidosis but also for several of the underlying inflammatory diseases that cause amyloid A amyloidosis have expanded leading to prolonged survival albeit frequently with renal failure. At the same time, there are also increasing numbers of patients diagnosed with one of the inherited forms of amyloidosis for which currently there is no targeted treatment available and, in some cases, renal failure is unavoidable. Due to the complex nature of the pathophysiology and treatment of these diseases, it can be very challenging for the clinician to determine whether or not it is appropriate to refer an affected individual for kidney transplantation. Determining eligibility criteria, as well as peritransplant and posttransplant management, requires a multidisciplinary approach with close monitoring and follow-up.

摘要

本文综述了系统性淀粉样变患者肾移植的最新进展和结局。淀粉样变可破坏肾脏的结构和功能,导致终末期肾病。近年来,治疗方法,尤其是针对轻链淀粉样变的治疗方法,以及引起淀粉样 A 淀粉样变的一些基础炎症性疾病的治疗方法,都有了进展,患者的生存时间得以延长,但常伴有肾衰竭。与此同时,越来越多的遗传性淀粉样变患者被诊断出来,目前尚无针对这些疾病的靶向治疗方法,在某些情况下,肾衰竭是不可避免的。由于这些疾病的病理生理学和治疗方法复杂,临床医生确定是否适合将受影响的个体转至肾移植科可能具有挑战性。确定资格标准,以及移植前和移植后管理,需要多学科方法,密切监测和随访。

相似文献

1
Kidney Transplantation in Systemic Amyloidosis.系统性淀粉样变性的肾移植。
Transplantation. 2020 Oct;104(10):2035-2047. doi: 10.1097/TP.0000000000003170.
2
Renal transplantation in amyloidosis and MIDD.淀粉样变性和线粒体糖尿病中的肾移植
Front Biosci (Elite Ed). 2015 Jan 1;7(1):149-57. doi: 10.2741/724.
3
Trends and causes of hospitalizations in patients with amyloidosis.淀粉样变性患者住院治疗的趋势及原因。
Amyloid. 2019 Sep;26(3):177-178. doi: 10.1080/13506129.2019.1618261. Epub 2019 Jun 7.
4
Systemic Amyloidosis and Kidney Transplantation: An Update.系统性淀粉样变与肾移植:最新进展
Semin Nephrol. 2024 Jan;44(1):151496. doi: 10.1016/j.semnephrol.2024.151496. Epub 2024 Mar 14.
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Amyloidosis and the Kidney: An Update.淀粉样变性与肾脏:更新。
Semin Nephrol. 2022 Nov;42(6):151343. doi: 10.1016/j.semnephrol.2023.151343. Epub 2023 May 4.
6
Emerging therapy in light-chain and acquired transthyretin-related amyloidosis: an Italian single-centre experience in heart transplantation.新型疗法在轻链和获得性转甲状腺素蛋白相关淀粉样变性中的应用:意大利单中心心脏移植经验。
J Cardiovasc Med (Hagerstown). 2021 Apr 1;22(4):261-267. doi: 10.2459/JCM.0000000000001094.
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Outcome of patients with amyloidosis after renal transplantation: a single-center experience.肾移植后淀粉样变性患者的结局:单中心经验
Int J Artif Organs. 2012 Jun;35(6):444-9. doi: 10.5301/ijao.5000091.
8
Among therapy modalities of end-stage renal disease, renal transplantation improves survival in patients with amyloidosis.在终末期肾病的治疗方式中,肾移植可提高淀粉样变性患者的生存率。
Transplant Proc. 2006 Mar;38(2):432-4. doi: 10.1016/j.transproceed.2005.12.051.
9
Renal Involvement in Systemic Amyloidosis Caused by Monoclonal Immunoglobulins.肾脏在单克隆免疫球蛋白引起的系统性淀粉样变性中的作用。
Hematol Oncol Clin North Am. 2020 Dec;34(6):1069-1079. doi: 10.1016/j.hoc.2020.08.002. Epub 2020 Sep 26.
10
Atrial fibrillation and subtype of atrial fibrillation in cardiac amyloidosis: clinical and echocardiographic features, impact on mortality.心脏淀粉样变中心房颤动和心房颤动亚型:临床和超声心动图特征及其对死亡率的影响。
Amyloid. 2019 Sep;26(3):128-138. doi: 10.1080/13506129.2019.1620724. Epub 2019 Jun 7.

引用本文的文献

1
An atypical cause of amyloidosis: a case of combined heavy and light chain amyloidosis.淀粉样变性的一种非典型病因:一例重链和轻链联合淀粉样变性病例
BMC Nephrol. 2025 Jul 1;26(1):332. doi: 10.1186/s12882-025-04226-9.
2
Combined Heart-Kidney Transplantation: Indications, Outcomes, and Controversies.心脏-肾脏联合移植:适应证、结果和争议。
Methodist Debakey Cardiovasc J. 2022 Sep 6;18(4):11-18. doi: 10.14797/mdcvj.1139. eCollection 2022.