Histiocytoid cardiomyopathy

Histiocytoid cardiomyopathy

Definition

Histiocytoid cardiomyopathy is an arrhythmogenic disorder characterized by cardiomegaly, severe cardiac arrhythmias or sudden death, and the presence of histiocyte-like cells within the myocardium.

Also known as Arachnocytosis of the myocardium, congenital cardiomyopathy, foamy myocardial transformation of infancy, histiocytoid cardiomyopathy, infantile cardiomyopathy with histiocytoid change, infantile xanthomatous cardiomyopathy, isolated Cardiac lipidosis, myocardial hamartoma, oncocytic cardiomyopathy, Purkinje cell hamartoma — per MONDO

Also identified as

Affected Organs

Organ Involvement Source
Cardiovascular system Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Cardiovascular system Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Heart Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Heart Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Respiratory system Disease Has Associated Anatomic Site NCIT · CC BY 4.0