Cardiac amyloidosis: a challenging diagnosis

Cardiovascular involvement of amyloidosis is present in 90% of cases, which is frequently associated with the primary form of the disease (AL amyloidosis). Clinical manifestations are represented by heart failure due to restrictive myocardiopathy and electrical impulse conduction abnormalities, whic...

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Main Authors: Graziele Cristina Palancio Morais, Marjorie Moreira Arruda, José Carlos de Aguiar Bonadia, Geanete Pozzan
Format: Article
Language:English
Published: University of São Paulo 2014-12-01
Series:Autopsy and Case Reports
Subjects:
Online Access:http://www.revistas.usp.br/autopsy/article/view/98461
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author Graziele Cristina Palancio Morais
Marjorie Moreira Arruda
José Carlos de Aguiar Bonadia
Geanete Pozzan
author_facet Graziele Cristina Palancio Morais
Marjorie Moreira Arruda
José Carlos de Aguiar Bonadia
Geanete Pozzan
author_sort Graziele Cristina Palancio Morais
collection DOAJ
description Cardiovascular involvement of amyloidosis is present in 90% of cases, which is frequently associated with the primary form of the disease (AL amyloidosis). Clinical manifestations are represented by heart failure due to restrictive myocardiopathy and electrical impulse conduction abnormalities, which are clinically remarkable in up to 50% of the cases. The prognosis of patients with systemic amyloidosis is directly associated with the presence of cardiac involvement, such that survival does not usually exceed 4 months after the onset of heart failure signs and symptoms. The authors report a case of primary systemic amyloidosis, diagnosed only at autopsy, with severe cardiac involvement.
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spelling doaj.art-d77dca8f1133498cadbcf691a55cbcf12022-12-22T03:10:16ZengUniversity of São PauloAutopsy and Case Reports2236-19602014-12-014410.4322/acr.%y.9846188479Cardiac amyloidosis: a challenging diagnosisGraziele Cristina Palancio Morais0Marjorie Moreira Arruda1José Carlos de Aguiar Bonadia2Geanete Pozzan3Department of Pathological Sciences – Faculdade de Ciências Médicas – Santa Casa de Misericórdia de São Paulo - São Paulo/SPDepartment of Pathological Sciences – Faculdade de Ciências Médicas – Santa Casa de Misericórdia de São Paulo - São Paulo/SPDepartment of Pathological Sciences – Faculdade de Ciências Médicas – Santa Casa de Misericórdia de São Paulo - São Paulo/SPDepartment of Pathological Sciences – Faculdade de Ciências Médicas – Santa Casa de Misericórdia de São Paulo - São Paulo/SPCardiovascular involvement of amyloidosis is present in 90% of cases, which is frequently associated with the primary form of the disease (AL amyloidosis). Clinical manifestations are represented by heart failure due to restrictive myocardiopathy and electrical impulse conduction abnormalities, which are clinically remarkable in up to 50% of the cases. The prognosis of patients with systemic amyloidosis is directly associated with the presence of cardiac involvement, such that survival does not usually exceed 4 months after the onset of heart failure signs and symptoms. The authors report a case of primary systemic amyloidosis, diagnosed only at autopsy, with severe cardiac involvement.http://www.revistas.usp.br/autopsy/article/view/98461AmyloidosisCardiomyopathyRestrictiveAutopsy
spellingShingle Graziele Cristina Palancio Morais
Marjorie Moreira Arruda
José Carlos de Aguiar Bonadia
Geanete Pozzan
Cardiac amyloidosis: a challenging diagnosis
Autopsy and Case Reports
Amyloidosis
Cardiomyopathy
Restrictive
Autopsy
title Cardiac amyloidosis: a challenging diagnosis
title_full Cardiac amyloidosis: a challenging diagnosis
title_fullStr Cardiac amyloidosis: a challenging diagnosis
title_full_unstemmed Cardiac amyloidosis: a challenging diagnosis
title_short Cardiac amyloidosis: a challenging diagnosis
title_sort cardiac amyloidosis a challenging diagnosis
topic Amyloidosis
Cardiomyopathy
Restrictive
Autopsy
url http://www.revistas.usp.br/autopsy/article/view/98461
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AT marjoriemoreiraarruda cardiacamyloidosisachallengingdiagnosis
AT josecarlosdeaguiarbonadia cardiacamyloidosisachallengingdiagnosis
AT geanetepozzan cardiacamyloidosisachallengingdiagnosis