Coexistence of Light Chain and Transthyretin Cardiac Amyloidosis.
cardiac amyloidosis
endomyocardial biopsy
light chain
transthyretin
Journal
JACC. Case reports
ISSN: 2666-0849
Titre abrégé: JACC Case Rep
Pays: Netherlands
ID NLM: 101757292
Informations de publication
Date de publication:
03 Apr 2024
03 Apr 2024
Historique:
received:
22
01
2024
revised:
07
02
2024
accepted:
12
02
2024
medline:
11
3
2024
pubmed:
11
3
2024
entrez:
11
3
2024
Statut:
epublish
Résumé
Although most patients with cardiac amyloidosis are diagnosed with either light chain (AL) or transthyretin (ATTR) disease, coexisting amyloid subtypes can occur. We present three cases of coexisting AL and ATTR cardiac amyloidosis and demonstrate the importance of clinical history and endomyocardial biopsy in diagnosis of this rare entity.
Identifiants
pubmed: 38465284
doi: 10.1016/j.jaccas.2024.102285
pii: S2666-0849(24)00066-4
pmc: PMC10918558
doi:
Types de publication
Case Reports
Langues
eng
Pagination
102285Informations de copyright
© 2024 The Authors.
Déclaration de conflit d'intérêts
The authors have reported that they have no relationships relevant to the contents of this paper to disclose.