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Case Report: AL Amyloidosis Severe Restrictive Cardiomyopathy Associated With Multiple Myeloma—Diagnostic Difficulties

BACKGROUND: Cardiac AL amyloidosis as a complication of multiple myeloma (MM) is a formidable life-threatening condition. The first-line therapy for both MM and systemic AL amyloidosis is proteasome inhibitors (PIs). Unfortunately, the use of PIs may lead to cardiovascular toxicity development, whic...

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Autores principales: Kirichenko, Yulia Y., Ilgisonis, Irina S., Nakhodnova, Elena S., Sokolova, Irina Y., Bochkarnikova, Olga V., Kardanova, Sabina A., Lyapidevskaya, Olga V., Privalova, Elena V., Ershov, Vladimir I., Belenkov, Yurii N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235537/
https://www.ncbi.nlm.nih.gov/pubmed/35770217
http://dx.doi.org/10.3389/fcvm.2022.862409
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author Kirichenko, Yulia Y.
Ilgisonis, Irina S.
Nakhodnova, Elena S.
Sokolova, Irina Y.
Bochkarnikova, Olga V.
Kardanova, Sabina A.
Lyapidevskaya, Olga V.
Privalova, Elena V.
Ershov, Vladimir I.
Belenkov, Yurii N.
author_facet Kirichenko, Yulia Y.
Ilgisonis, Irina S.
Nakhodnova, Elena S.
Sokolova, Irina Y.
Bochkarnikova, Olga V.
Kardanova, Sabina A.
Lyapidevskaya, Olga V.
Privalova, Elena V.
Ershov, Vladimir I.
Belenkov, Yurii N.
author_sort Kirichenko, Yulia Y.
collection PubMed
description BACKGROUND: Cardiac AL amyloidosis as a complication of multiple myeloma (MM) is a formidable life-threatening condition. The first-line therapy for both MM and systemic AL amyloidosis is proteasome inhibitors (PIs). Unfortunately, the use of PIs may lead to cardiovascular toxicity development, which requires specific cardio-oncology supervision. CASE REPORT: A 57-year-old woman was admitted to a university hospital with clinical manifestation of progressive chronic heart failure. The patient had hypertension and no history of diabetes mellitus, myocardial infarction (MI), stroke, and arrhythmias. After a series of laboratory and instrumental examination methods, MM complicated by cardiac AL amyloidosis was proved. Upon specific cardio-oncology examination (NT-proBNP 4,274 pg/ml), ECHO showed systolic dysfunction, motion abnormalities in LV basal and middle segments, and a typical depositional myocardium pattern (“luminescence”); cardiac MRI revealed restrictive cardiomyopathy and specific hyperenhancement of the ventricles and atria; 24-h ECG showed QS-pattern in leads V1–V3 and unstable ventricular tachycardia (VT) paroxysms. Cardio-oncology consultation showed baseline cardiovascular risk was very high (≥20%), and cardioprotective therapy [iACE/ARBs, beta-blockers (BB), statins] was administered. The patient underwent VCD (bortezomib; cyclophosphamide; dexamethasone) chemotherapy (CMT) program. By the time of publication, the patient had received four CMT courses with a positive oncohematological and cardiovascular effect. CONCLUSION: In this clinical case, we described a complication of MM, which was rare according to the severity and manifestation with restrictive cardiomyopathy due to secondary cardiac amyloidosis. The case's features were difficulties in verifying the underlying disease and its own complication, and the complexity of patient management according to modern principles of cardio-oncology.
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spelling pubmed-92355372022-06-28 Case Report: AL Amyloidosis Severe Restrictive Cardiomyopathy Associated With Multiple Myeloma—Diagnostic Difficulties Kirichenko, Yulia Y. Ilgisonis, Irina S. Nakhodnova, Elena S. Sokolova, Irina Y. Bochkarnikova, Olga V. Kardanova, Sabina A. Lyapidevskaya, Olga V. Privalova, Elena V. Ershov, Vladimir I. Belenkov, Yurii N. Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Cardiac AL amyloidosis as a complication of multiple myeloma (MM) is a formidable life-threatening condition. The first-line therapy for both MM and systemic AL amyloidosis is proteasome inhibitors (PIs). Unfortunately, the use of PIs may lead to cardiovascular toxicity development, which requires specific cardio-oncology supervision. CASE REPORT: A 57-year-old woman was admitted to a university hospital with clinical manifestation of progressive chronic heart failure. The patient had hypertension and no history of diabetes mellitus, myocardial infarction (MI), stroke, and arrhythmias. After a series of laboratory and instrumental examination methods, MM complicated by cardiac AL amyloidosis was proved. Upon specific cardio-oncology examination (NT-proBNP 4,274 pg/ml), ECHO showed systolic dysfunction, motion abnormalities in LV basal and middle segments, and a typical depositional myocardium pattern (“luminescence”); cardiac MRI revealed restrictive cardiomyopathy and specific hyperenhancement of the ventricles and atria; 24-h ECG showed QS-pattern in leads V1–V3 and unstable ventricular tachycardia (VT) paroxysms. Cardio-oncology consultation showed baseline cardiovascular risk was very high (≥20%), and cardioprotective therapy [iACE/ARBs, beta-blockers (BB), statins] was administered. The patient underwent VCD (bortezomib; cyclophosphamide; dexamethasone) chemotherapy (CMT) program. By the time of publication, the patient had received four CMT courses with a positive oncohematological and cardiovascular effect. CONCLUSION: In this clinical case, we described a complication of MM, which was rare according to the severity and manifestation with restrictive cardiomyopathy due to secondary cardiac amyloidosis. The case's features were difficulties in verifying the underlying disease and its own complication, and the complexity of patient management according to modern principles of cardio-oncology. Frontiers Media S.A. 2022-06-13 /pmc/articles/PMC9235537/ /pubmed/35770217 http://dx.doi.org/10.3389/fcvm.2022.862409 Text en Copyright © 2022 Kirichenko, Ilgisonis, Nakhodnova, Sokolova, Bochkarnikova, Kardanova, Lyapidevskaya, Privalova, Ershov and Belenkov. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Kirichenko, Yulia Y.
Ilgisonis, Irina S.
Nakhodnova, Elena S.
Sokolova, Irina Y.
Bochkarnikova, Olga V.
Kardanova, Sabina A.
Lyapidevskaya, Olga V.
Privalova, Elena V.
Ershov, Vladimir I.
Belenkov, Yurii N.
Case Report: AL Amyloidosis Severe Restrictive Cardiomyopathy Associated With Multiple Myeloma—Diagnostic Difficulties
title Case Report: AL Amyloidosis Severe Restrictive Cardiomyopathy Associated With Multiple Myeloma—Diagnostic Difficulties
title_full Case Report: AL Amyloidosis Severe Restrictive Cardiomyopathy Associated With Multiple Myeloma—Diagnostic Difficulties
title_fullStr Case Report: AL Amyloidosis Severe Restrictive Cardiomyopathy Associated With Multiple Myeloma—Diagnostic Difficulties
title_full_unstemmed Case Report: AL Amyloidosis Severe Restrictive Cardiomyopathy Associated With Multiple Myeloma—Diagnostic Difficulties
title_short Case Report: AL Amyloidosis Severe Restrictive Cardiomyopathy Associated With Multiple Myeloma—Diagnostic Difficulties
title_sort case report: al amyloidosis severe restrictive cardiomyopathy associated with multiple myeloma—diagnostic difficulties
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235537/
https://www.ncbi.nlm.nih.gov/pubmed/35770217
http://dx.doi.org/10.3389/fcvm.2022.862409
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