ASNC/AHA/ASE/EANM/HFSA/ISA/SCMR/SNMMI expert consensus recommendations for multimodality imaging in cardiac amyloidosis: part 1 of 2—evidence base …

S Dorbala, Y Ando, S Bokhari… - Circulation …, 2021 - Am Heart Assoc
Sharmila Dorbala, MD, MPH, FASNC, Chair*; Yukio Ando, MD, PhD†; Sabahat Bokhari,
MD‡; Angela Dispenzieri, MD § ; Rodney H. Falk, MD*; Victor A. Ferrari, MD∥; Marianna …

Two types of amyloidosis presenting in a single patient: a case series

MH Sidiqi, ED McPhail, JD Theis, S Dasari… - Blood cancer …, 2019 - nature.com
The amyloidoses are a group of disorders with overlapping clinical presentations,
characterized by aggregation and tissue deposition of misfolded proteins. The nature and …

A risk score to diagnose cardiac involvement and provide prognosis information in patients at risk of cardiac light-chain amyloidosis

Y Wu, C Pu, W Zhu, C He, J Fei, H Hu - Frontiers in Cardiovascular …, 2022 - frontiersin.org
Background Cardiac light-chain amyloidosis (AL CA) portends poor prognosis. Contrast
cardiac magnetic resonance (CMR) with late gadolinium enhancement (LGE) imaging is an …

Non‐cardiac biopsy sites with high frequency of transthyretin amyloidosis

S Dasari, A Dispenzieri, S Mansour, P Muppa… - ESC Heart …, 2021 - Wiley Online Library
Aims Cardiac scintigraphy, a non‐invasive technique for diagnosing ATTR cardiac
amyloidosis, lacks specificity in patients with concomitant monoclonal gammopathy (up to …

Case Report: Avoiding misdiagnosis in amyloidosis—navigating transthyretin genopositivity and monoclonal gammopathy in a patient with advanced heart failure and …

X Wu, D Toskic, P Zhou, S Scalia, X Ma… - Frontiers in …, 2024 - frontiersin.org
Background A 63-year-old Black woman presented with progressive exertional dyspnea and
chronic lower back pain. The course and findings in her case are instructive. Case report …

Autopsy case with concurrent transthyretin and immunoglobulin amyloidosis

Y Shintani‐Domoto, K Ishino, H Naiki… - Pathology …, 2022 - Wiley Online Library
An 85‐year‐old man with a history of aortic dissection suddenly fainted, underwent cardiac
heart arrest, and died. An autopsy was performed, but the cause of death was not grossly …

Transthyretin Cardiac Amyloidosis Disguised as Light Chain Amyloidosis or Multiple Myeloma?

AP Stein, EL Matthia, SA Petty, B Stewart… - The American Journal of …, 2024 - Elsevier
Highlights•To appreciate the challenges behind correctly identifying cardiac amyloidosis
subtypes.•To emphasize the essential role of endomyocardial biopsy and mass …

Поражение сердца при сочетанных формах системного амилоидоза

МГ Рыбакова, МТ Власова, ИА Кузнецова… - Архив патологии, 2021 - elibrary.ru
Сердечно-сосудистая система является частой мишенью системного амилоидоза (сА),
наиболее изученными являются AL-сА, дикий (ATTRwt-сА) и мутированный (ATTRmt …

[HTML][HTML] Two Kinds of Cardiac Amyloidosis in One Patient: A Case Report

AL Yu, CH Tsai, CC Chao, CT Shun… - Acta Cardiologica …, 2022 - ncbi.nlm.nih.gov
Amyloidosis is a progressive and debilitating disease that can be systemic or organ-limited.
It results from insoluble homomeric amyloid fibrils, composed of a variety of serum proteins …

Two types of amyloidosis presenting in a single patient: a case series

SM Hasib, ED McPhail, JD Theis… - Blood Cancer …, 2019 - search.proquest.com
The amyloidoses are a group of disorders with overlapping clinical presentations,
characterized by aggregation and tissue deposition of misfolded proteins. The nature and …