The pathology of amyloidosis in classification: a review

MM Picken - Acta haematologica, 2020 - karger.com
Background: The amyloidoses are a rare and heterogeneous group of disorders that are
characterized by the deposition of abnormally folded proteins in tissues ultimately leading to …

Atrial fibrillation in the setting of cardiac amyloidosis–A review of the literature

G Bazoukis, A Saplaouras, P Efthymiou… - Journal of …, 2024 - Elsevier
Cardiac amyloidosis (CA) is related to the aggregation of insoluble fibrous deposits of
misfolded proteins within the myocardium. Transthyretin amyloidosis (ATTR) and …

[HTML][HTML] 2023 Expert Consensus of the Taiwan Society of Cardiology on the Diagnosis and Treatment of Cardiac Amyloidosis

CC Wang, WT Chang, YH Lin, BH Tzeng… - Acta Cardiologica …, 2023 - ncbi.nlm.nih.gov
Cardiac amyloidosis is one form of systemic amyloidosis caused by abnormal amyloid fibrils
deposited in the extracellular space of the myocardium causing heart failure because of …

New oral anticoagulants vs. vitamin K antagonists among patients with cardiac amyloidosis: prognostic impact

E Cariou, K Sanchis, K Rguez, V Blanchard… - Frontiers in …, 2021 - frontiersin.org
Background: Atrial arrhythmia (AA) is common among patients with cardiac amyloidosis
(CA), who have an increased risk of intracardiac thrombus. The aim of this study was to …

[HTML][HTML] Distinctive Deposition Patterns of Sporadic Transthyretin-Derived Amyloidosis in the Atria: A Forensic Autopsy-Based Study

S Ichimata, Y Hata, K Yoshida, K Hirono… - International Journal of …, 2024 - mdpi.com
Left-to-right differences in the histopathologic patterns of transthyretin-derived amyloid
(ATTR) deposition in the atria of older adults have not yet been investigated. Hence, this …

[HTML][HTML] Histopathological and Immunohistochemical Characteristics of Different Types of Cardiac Amyloidosis

ZV Gioeva, LM Mikhaleva, NA Gutyrchik… - International Journal of …, 2024 - mdpi.com
Cardiac involvement is the most important factor determining prognosis in patients with
systemic amyloidosis. This retrospective observational study of 98 patients with amyloidosis …

Cardiac amyloidosis: a clinical and pathological review

JJ Maleszewski - Diagnostic Histopathology, 2022 - Elsevier
Amyloidosis is a broad class of diseases all of which result in deposition of misfolded
extracellular protein that result in organ dysfunction. Once considered a rare condition …

Transthyretin derived amyloid deposits in the atrium and the aortic valve: insights from multimodality evaluations and mid-term follow up

A Okada, T Kakuta, N Tadokoro, E Tateishi… - BMC Cardiovascular …, 2023 - Springer
Background Recent studies have reported atrial involvement and coexistence of aortic
stenosis in transthyretin (ATTR) cardiac amyloidosis (CA). However, pathological reports of …

Coexisting transthyretin and atrial natriuretic peptide amyloid on left atrium in transthyretin amyloid cardiomyopathy

N Kuyama, S Takashio, K Nakamura… - Journal of Cardiology …, 2024 - Elsevier
Atrial amyloidosis is primarily caused by atrial natriuretic peptide (ANP) amyloid deposition.
The main precursor protein causing cardiac amyloidosis is transthyretin (TTR), also known …

Clinical implications of atrial natriuretic peptide amyloidosis

C Hyer, C Campbell, R Kahwash - BMJ Case Reports CP, 2021 - casereports.bmj.com
A 74-year-old woman with a history of diastolic heart failure and refractory atrial fibrillation
(AF) presented with unstable angina for coronary artery bypass grafting. Routine …