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Approach to a patient with cardiac amyloidosis.

作者信息

Strouse Christopher, Briasoulis Alexandros, Fonseca Rafael, Jethava Yogesh

机构信息

Department of Internal Medicine, Division of Hematology, Oncology, and Blood and Marrow Transplantation, University of Iowa, Iowa City, IA, USA.

Cardiomyopathy Section, Cardiology Division, University of Iowa, Iowa City, Iowa, USA.

出版信息

J Geriatr Cardiol. 2019 Jul;16(7):567-574. doi: 10.11909/j.issn.1671-5411.2019.07.010.

DOI:10.11909/j.issn.1671-5411.2019.07.010
PMID:31447895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6689519/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/551d/6689519/f534951dc1cd/jgc-16-07-567-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/551d/6689519/f534951dc1cd/jgc-16-07-567-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/551d/6689519/f534951dc1cd/jgc-16-07-567-g001.jpg

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本文引用的文献

1
Grading cardiac response in AL amyloidosis: implications for relapse and survival.
Br J Haematol. 2019 Jul;186(1):144-146. doi: 10.1111/bjh.15717. Epub 2018 Dec 19.
2
Clinical and endoscopic manifestations of gastrointestinal amyloidosis: a case series.胃肠道淀粉样变性的临床和内镜表现：病例系列
Clujul Med. 2018 Oct;91(4):469-473. doi: 10.15386/cjmed-951. Epub 2018 Oct 30.
3
Deferred autologous stem cell transplantation in systemic AL amyloidosis.系统性淀粉样变病中的延迟自体干细胞移植。
用锝-焦磷酸盐（PYP）定量单光子发射计算机断层扫描评估心脏淀粉样变性。
EJNMMI Phys. 2021 Jan 7;8(1):3. doi: 10.1186/s40658-020-00342-7.
4
A key role for comprehensive geriatric assessment in aortic valve replacement.全面老年评估在主动脉瓣置换中的关键作用。
BMJ Case Rep. 2020 Dec 22;13(12):e237031. doi: 10.1136/bcr-2020-237031.
5
Cardiac amyloidosis presenting with recurrent ischaemic strokes.以复发性缺血性中风为表现的心脏淀粉样变性
BMJ Case Rep. 2020 Feb 23;13(2):e231910. doi: 10.1136/bcr-2019-231910.
Blood Cancer J. 2018 Nov 5;8(11):101. doi: 10.1038/s41408-018-0137-9.
4
Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy.特发性甲状腺素运载蛋白淀粉样变心肌病患者的塔法米迪治疗。
N Engl J Med. 2018 Sep 13;379(11):1007-1016. doi: 10.1056/NEJMoa1805689. Epub 2018 Aug 27.
5
Outcome of Patients With Newly Diagnosed Systemic Light-Chain Amyloidosis Associated With Deletion of 17p.新诊断的与17p缺失相关的系统性轻链淀粉样变性患者的预后
Clin Lymphoma Myeloma Leuk. 2018 Nov;18(11):e493-e499. doi: 10.1016/j.clml.2018.07.292. Epub 2018 Jul 25.
6
Impact of Induction Therapy on the Outcome of Immunoglobulin Light Chain Amyloidosis after Autologous Hematopoietic Stem Cell Transplantation.自体造血干细胞移植后诱导治疗对免疫球蛋白轻链淀粉样变性患者结局的影响。
Biol Blood Marrow Transplant. 2018 Nov;24(11):2197-2203. doi: 10.1016/j.bbmt.2018.07.010. Epub 2018 Aug 9.
7
Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis.依洛瑟那治疗遗传性转甲状腺素蛋白淀粉样变性病患者。
N Engl J Med. 2018 Jul 5;379(1):22-31. doi: 10.1056/NEJMoa1716793.
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Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis.用于遗传性转甲状腺素蛋白淀粉样变性的 RNAi 治疗药物 Patisiran
N Engl J Med. 2018 Jul 5;379(1):11-21. doi: 10.1056/NEJMoa1716153.
9
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