A patient with pulmonary hypertension: a rare case of AL amyloidosis involving the heart and external auditory canal
Author:
Affiliation:
1. Petrozavodsk State University, Petrozavodsk; Baranov Republican Hospital
2. Baranov Republican Hospital
Abstract
Publisher
Silicea - Poligraf, LLC
Reference19 articles.
1. Humbert M, Kovacs G, Hoeper MM, et al. 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension. Eur Heart J. 2022;43(38):3618-731. doi:10.1093/eurheartj/ehac237.
2. Donnelly J, Hanna M.Cardiac amyloidosis: An update on diagnosis and treatment. Cleve Clin J Med. 2017;84(12 Suppl 3):12-26. doi:10.3949/ccjm.84.s3.02.
3. Muchtar E, Dispenzieri A, Magen H, et al. Systemic amyloidosis from A (AA) to T (ATTR): a review. J Intern Med. 2021;289(3):268-92. doi:10.1111/joim.13169.
4. Tereshchenko SN, Zhirov IV, Moiseeva OM, et al. Practical guidelines for the diagnosis and treatment of transthyretin amyloid cardiomyopathy (ATTR-CM or transthyretin cardiac amyloidosis). Terapevticheskii Arkhiv. 2022;94(4):584-95. (In Russ.) doi:10.26442/00403660.2022.04.201465.
5. Kittleson MM, Ruberg FL, Ambardekar AV, et al. 2023 ACC Expert Consensus Decision Pathway on Comprehensive Multidisciplinary Care for the Patient With Cardiac Amyloidosis: A Report of the American College of Cardiology Solution Set Oversight Committee. J Am Coll Cardiol. 2023;81(11):1076-126. doi:10.1016/j.jacc.2022.11.022.
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