Cardiomyopathy (WHO/ISFC 1995 classification)

Cardiomyopathy

(WHO/ISFC 1995 classification) • Apical non-obstructive hypertrophic cardiomyopathy (Yamaguchi hypertrophy) - Ganzer Fall bei Radiopaedia

Jha P, Apical non-obstructive hypertrophic cardiomyopathy (Yamaguchi hypertrophy). Case study, Radiopaedia.org (Accessed on 07 Dec 2022) https://doi.org/10.53347/rID-16177 • CC by-nc-sa 3.0 (modified)

Cardiomyopathy

(WHO/ISFC 1995 classification) • Dilated cardiomyopathy - Ganzer Fall bei Radiopaedia

Jha P, Dilated cardiomyopathy. Case study, Radiopaedia.org (Accessed on 07 Dec 2022) https://doi.org/10.53347/rID-16203 • CC by-nc-sa 3.0 (modified)

Cardiomyopathy

(WHO/ISFC 1995 classification) • Tachycardia-induced cardiomyopathy - Ganzer Fall bei Radiopaedia

Ranadive A, Tachycardia-induced cardiomyopathy. Case study, Radiopaedia.org (Accessed on 07 Dec 2022) https://doi.org/10.53347/rID-56426 • CC by-nc-sa 3.0 (modified)

Cardiomyopathy

(WHO/ISFC 1995 classification) • Hypertrophic cardiomyopathy with cor triatriatum - Ganzer Fall bei Radiopaedia

Tatco V, Hypertrophic cardiomyopathy with cor triatriatum. Case study, Radiopaedia.org (Accessed on 07 Dec 2022) https://doi.org/10.53347/rID-44339 • CC by-nc-sa 3.0 (modified)

Cardiomyopathy

(WHO/ISFC 1995 classification) • Active right ventricular cardiac sarcoidosis - Ganzer Fall bei Radiopaedia

Elgendy A, Active right ventricular cardiac sarcoidosis. Case study, Radiopaedia.org (Accessed on 07 Dec 2022) https://doi.org/10.53347/rID-55596 • CC by-nc-sa 3.0 (modified)

Cardiomyopathy

(WHO/ISFC 1995 classification) • Post-partum cardiomyopathy - Ganzer Fall bei Radiopaedia

Knipe H, Post-partum cardiomyopathy. Case study, Radiopaedia.org (Accessed on 07 Dec 2022) https://doi.org/10.53347/rID-47443 • CC by-nc-sa 3.0 (modified)

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Cardiomyopathy classification separates the various cardiomyopathies into several subtypes. Cardiomyopathy is defined as a "disease of the myocardium with associated cardiac dysfunction".

It was initially classified according to the 1995 World Health Organization / International Society and Federation of Cardiology (WHO/ISFC) system as follows:

dilated cardiomyopathy
hypertrophic cardiomyopathy
restrictive cardiomyopathy
arrhythmogenic right ventricular cardiomyopathy
specific cardiomyopathy
non-classified cardiomyopathies which include
- fibroelastosis
- mildly dilated cardiomyopathy
- non-compacted myocardium
- mitochondrial cardiomyopathy

This has since been revised in 2006 by the American Heart Association (AHA) as follows :

primary cardiomyopathies predominantly involving the heart
- genetic
  - hypertrophic cardiomyopathy
    - cardiomyopathy from primary cardiac glycogen storage diseases (PRKAG2 cardiac syndrome, Danon disease)
  - arrhythmogenic right ventricular cardiomyopathy
  - left ventricular non-compaction
  - cardiomyopathy from conduction defects
  - cardiomyopathies from ion channelopathies (e.g. long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, short QT syndrome)
  - cardiomyopathies from mitochondrial myopathies
- mixed
  - dilated cardiomyopathy
  - restrictive cardiomyopathy
- acquired
  - inflammatory cardiomyopathy (i.e. myocarditis)
  - stress-induced cardiomyopathy (i.e. Takotsubo cardiomyopathy)
  - cardiomyopathy in peripartum and postpartum cardiomyopathy
  - tachycardia-induced cardiomyopathy
  - cardiomyopathy in infants of diabetic mothers
secondary cardiomyopathies (these conditions can have multi-organ involvement)
- infiltrative conditions - cardiomyopathy from
  - cardiac amyloidosis
  - Gaucher disease
  - Hurler disease
  - Hunter disease
- cardiomyopathy from storage conditions
  - cardiomyopathy in hemochromatosis
  - Fabry disease
  - systemic glycogen storage disease (e.g. Pompe disease)
  - Niemann-Pick disease
- cardiomyopathy from toxic agents
  - drugs, heavy metals, chemicals
- cardiomyopathy from endomyocardial causes
  - endomyocardial fibrosis
  - Loeffler endocarditis
- cardiomyopathy from systemic inflammatory conditions
  - cardiac sarcoidosis
- cardiomyopathy from underlying systemic autoimmune conditions
- cardiomyopathy from endocrine conditions
- cardiomyopathy from neuromuscular conditions
- cardiomyopathy from underlying nutritional conditions
  - beriberi
  - pellagra
  - scurvy
  - selenium deficiency
  - carnitine deficiency
- cardiomyopathy from underlying electrolyte imbalances
  - potassium
  - magnesium
  - phosphate
- cardiomyopathy related to cancer treatment
  - doxorubicin cardiotoxicity
  - cyclophosphamide cardiotoxicity
  - radiation cardiotoxicity