IntroductionThis study examined the role of echocardiographic and cardiac histomorphology parameters in predicting mortality in patients with cardiac AL amyloidosis.MethodsPatients with endomyocardial biopsy-proven cardiac AL amyloidosis treated at MD Anderson Cancer Center between 6/2011 and 6/2020 were identified. Stored echocardiographic images and endomyocardial biopsy samples were processed for myocardial strain analysis and a detailed histomorphology characterization.ResultsOf 43 patients; 44% were women and 63% white. Median age was 65 years; 51% underwent stem cell transplantation (SCT). Thirty patients (70%) died during follow up (median follow up: 4.1 years). Lower LA strain (ConclusionLower LA strain independently predicted morta...
Background: Clinical recognition of cardiac involvement and cardiac response to therapy is an import...
ObjectivesThe aim of the study was to determine whether longitudinal left ventricular (LV) function ...
BACKGROUND: Light chain (AL) and transthyretin (ATTR) amyloid fibrils are deposited in the extracell...
Objectives: The aim was to determine the role of assessing right ventricular (RV) function, using st...
BACKGROUND: The prognostic value of Doppler myocardial imaging, including myocardial velocity imagi...
. These authors contributed equally to this work. Objectives: Since diastolic abnormalities are typi...
AIM: Amyloidosis is a systemic disease, related to different underlying causes, with frequent cardia...
Objectives: Since diastolic abnormalities are typical findings of cardiac amyloidosis (CA), we hypot...
Objectives: Since diastolic abnormalities are typical findings of cardiac amyloidosis (CA), we hypot...
Primary light-chain (AL) amyloidosis is a plasma cell dyscrasia associated with the deposition of im...
Cardiac amyloidosis (CA) is of poor prognosis and has three main causes: light chain (AL), hereditar...
BACKGROUND: Patients with AL amyloidosis often present with signs of congestive heart failure. AIM: ...
Background: T1 mapping allows quantitative assessment of “diffuse” deposition of amyloid protein in ...
BACKGROUND: Prognosis in light-chain (AL) and transthyretin (ATTR) amyloidosis is influenced by card...
Primary light-chain (AL) amyloidosis is a plasma cell dyscrasia associated with the deposition of im...
Background: Clinical recognition of cardiac involvement and cardiac response to therapy is an import...
ObjectivesThe aim of the study was to determine whether longitudinal left ventricular (LV) function ...
BACKGROUND: Light chain (AL) and transthyretin (ATTR) amyloid fibrils are deposited in the extracell...
Objectives: The aim was to determine the role of assessing right ventricular (RV) function, using st...
BACKGROUND: The prognostic value of Doppler myocardial imaging, including myocardial velocity imagi...
. These authors contributed equally to this work. Objectives: Since diastolic abnormalities are typi...
AIM: Amyloidosis is a systemic disease, related to different underlying causes, with frequent cardia...
Objectives: Since diastolic abnormalities are typical findings of cardiac amyloidosis (CA), we hypot...
Objectives: Since diastolic abnormalities are typical findings of cardiac amyloidosis (CA), we hypot...
Primary light-chain (AL) amyloidosis is a plasma cell dyscrasia associated with the deposition of im...
Cardiac amyloidosis (CA) is of poor prognosis and has three main causes: light chain (AL), hereditar...
BACKGROUND: Patients with AL amyloidosis often present with signs of congestive heart failure. AIM: ...
Background: T1 mapping allows quantitative assessment of “diffuse” deposition of amyloid protein in ...
BACKGROUND: Prognosis in light-chain (AL) and transthyretin (ATTR) amyloidosis is influenced by card...
Primary light-chain (AL) amyloidosis is a plasma cell dyscrasia associated with the deposition of im...
Background: Clinical recognition of cardiac involvement and cardiac response to therapy is an import...
ObjectivesThe aim of the study was to determine whether longitudinal left ventricular (LV) function ...
BACKGROUND: Light chain (AL) and transthyretin (ATTR) amyloid fibrils are deposited in the extracell...