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The role of echocardiography and (99m)Tc-HDP scintigraphy in non-invasive diagnosis of cardiac amyloidosis: A case series and literature review

RATIONALE: Cardiac amyloidosis, considered for the last years to be a rare disease, is one of the determinants of HFpEF. The non-specific clinical presentation and the difficulties related to endomyocardial biopsy have made cardiac amyloidosis an underdiagnosed clinical entity. Improvement of non-in...

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Autores principales: Costache, Irina Iuliana, Buburuz, Ana Maria, Crisu, Daniela, Statescu, Ana Maria, Ungureanu, Carmen, Aursulesei, Viviana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756609/
https://www.ncbi.nlm.nih.gov/pubmed/31567998
http://dx.doi.org/10.1097/MD.0000000000017256
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author Costache, Irina Iuliana
Buburuz, Ana Maria
Crisu, Daniela
Statescu, Ana Maria
Ungureanu, Carmen
Aursulesei, Viviana
author_facet Costache, Irina Iuliana
Buburuz, Ana Maria
Crisu, Daniela
Statescu, Ana Maria
Ungureanu, Carmen
Aursulesei, Viviana
author_sort Costache, Irina Iuliana
collection PubMed
description RATIONALE: Cardiac amyloidosis, considered for the last years to be a rare disease, is one of the determinants of HFpEF. The non-specific clinical presentation and the difficulties related to endomyocardial biopsy have made cardiac amyloidosis an underdiagnosed clinical entity. Improvement of non-invasive diagnostic techniques and the development of new therapies increased clinical awareness for this form of restrictive cardiomyopathy. We here summarize echocardiography and (99m)Tc-HDP scintigraphy findings in 6 cases of cardiac amyloidosis and review the literature data of this progressive and fatal cardiomyopathy. PATIENTS CONCERNS: The main clinical manifestations were fatigue, low exercise tolerance and edemas. The right heart failure symptoms usually dominated the clinical picture. DIAGNOSES: All cases were evaluated by echocardiography; 3 cases were further examined by bone scintigraphy and 4 cases a peripheral biopsy was performed. Electrocardiography showed low-voltage QRS complexes and “pseudo-infarct” pattern in the precordial leads, contrary to the echocardiographic aspect, which revealed thickening of ventricle walls. Biatrial dilation and diastolic disfunction were observed. Impaired systolic function was detected in advanced stages of the disease. (99m)Tc-HDP scintigraphy revealed cardiac uptake of radiopharmaceutical and managed to confirm the diagnosis in 1 case of cardiac amyloidosis in which salivary gland biopsy was negative. INTERVENTIONS: The treatment was based on managing fluid balance, with the mainstream therapy represented by diuretics. Neurohormonal agents, usually used in heart failure treatment were avoided, due to poor tolerance and worsening of disease course. The management of these 6 cases was challenging due to the refractory manifestation of congestive heart failure. OUTCOMES: During follow-up, 4 of the 6 patients from the current study died in the first year after the final diagnosis was established. LESSONS: Nuclear imaging of cardiac amyloidosis has a revolutionary development nowadays. Bone scintigraphy presents promising results for identifying patients at early stages of disease and to differentiate between cardiac amyloidosis types. Further studies are necessary for the standardization of imaging protocol and development of non-invasive diagnostic tools, especially in assessing the response to treatment and disease progression, for which little is known.
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spelling pubmed-67566092019-10-07 The role of echocardiography and (99m)Tc-HDP scintigraphy in non-invasive diagnosis of cardiac amyloidosis: A case series and literature review Costache, Irina Iuliana Buburuz, Ana Maria Crisu, Daniela Statescu, Ana Maria Ungureanu, Carmen Aursulesei, Viviana Medicine (Baltimore) 3400 RATIONALE: Cardiac amyloidosis, considered for the last years to be a rare disease, is one of the determinants of HFpEF. The non-specific clinical presentation and the difficulties related to endomyocardial biopsy have made cardiac amyloidosis an underdiagnosed clinical entity. Improvement of non-invasive diagnostic techniques and the development of new therapies increased clinical awareness for this form of restrictive cardiomyopathy. We here summarize echocardiography and (99m)Tc-HDP scintigraphy findings in 6 cases of cardiac amyloidosis and review the literature data of this progressive and fatal cardiomyopathy. PATIENTS CONCERNS: The main clinical manifestations were fatigue, low exercise tolerance and edemas. The right heart failure symptoms usually dominated the clinical picture. DIAGNOSES: All cases were evaluated by echocardiography; 3 cases were further examined by bone scintigraphy and 4 cases a peripheral biopsy was performed. Electrocardiography showed low-voltage QRS complexes and “pseudo-infarct” pattern in the precordial leads, contrary to the echocardiographic aspect, which revealed thickening of ventricle walls. Biatrial dilation and diastolic disfunction were observed. Impaired systolic function was detected in advanced stages of the disease. (99m)Tc-HDP scintigraphy revealed cardiac uptake of radiopharmaceutical and managed to confirm the diagnosis in 1 case of cardiac amyloidosis in which salivary gland biopsy was negative. INTERVENTIONS: The treatment was based on managing fluid balance, with the mainstream therapy represented by diuretics. Neurohormonal agents, usually used in heart failure treatment were avoided, due to poor tolerance and worsening of disease course. The management of these 6 cases was challenging due to the refractory manifestation of congestive heart failure. OUTCOMES: During follow-up, 4 of the 6 patients from the current study died in the first year after the final diagnosis was established. LESSONS: Nuclear imaging of cardiac amyloidosis has a revolutionary development nowadays. Bone scintigraphy presents promising results for identifying patients at early stages of disease and to differentiate between cardiac amyloidosis types. Further studies are necessary for the standardization of imaging protocol and development of non-invasive diagnostic tools, especially in assessing the response to treatment and disease progression, for which little is known. Wolters Kluwer Health 2019-09-20 /pmc/articles/PMC6756609/ /pubmed/31567998 http://dx.doi.org/10.1097/MD.0000000000017256 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 3400
Costache, Irina Iuliana
Buburuz, Ana Maria
Crisu, Daniela
Statescu, Ana Maria
Ungureanu, Carmen
Aursulesei, Viviana
The role of echocardiography and (99m)Tc-HDP scintigraphy in non-invasive diagnosis of cardiac amyloidosis: A case series and literature review
title The role of echocardiography and (99m)Tc-HDP scintigraphy in non-invasive diagnosis of cardiac amyloidosis: A case series and literature review
title_full The role of echocardiography and (99m)Tc-HDP scintigraphy in non-invasive diagnosis of cardiac amyloidosis: A case series and literature review
title_fullStr The role of echocardiography and (99m)Tc-HDP scintigraphy in non-invasive diagnosis of cardiac amyloidosis: A case series and literature review
title_full_unstemmed The role of echocardiography and (99m)Tc-HDP scintigraphy in non-invasive diagnosis of cardiac amyloidosis: A case series and literature review
title_short The role of echocardiography and (99m)Tc-HDP scintigraphy in non-invasive diagnosis of cardiac amyloidosis: A case series and literature review
title_sort role of echocardiography and (99m)tc-hdp scintigraphy in non-invasive diagnosis of cardiac amyloidosis: a case series and literature review
topic 3400
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756609/
https://www.ncbi.nlm.nih.gov/pubmed/31567998
http://dx.doi.org/10.1097/MD.0000000000017256
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