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Dilated Cardiomyopathy Phenotype With Global (Four-Chamber) Involvement in a Cat: Echocardiographic, Pathological,
Giovanni Romito1, Alessandra Costa1, Maria Morini1
1Department of Veterinary Medical Sciences, Alma Mater Studiorum-University of Bologna, Ozzano dell'Emilia, Italy.
Insights
A rare case of feline dilated cardiomyopathy (DCM) was diagnosed in an Exotic Shorthair cat. Postmortem findings revealed characteristic cardiac abnormalities, supporting this rare diagnosis in cats.
Area of Science:
- Veterinary Cardiology
- Feline Medicine
- Cardiovascular Pathology
Background:
- Dilated cardiomyopathy (DCM) is a primary myocardial disease characterized by ventricular dilation and systolic dysfunction.
- While DCM is well-documented in humans and dogs, it is considered rare in cats, with hypertrophic cardiomyopathy being more prevalent.
- This case presents a unique instance of DCM in a feline patient, necessitating detailed investigation.
Purpose of the Study:
- To document and characterize a rare case of feline dilated cardiomyopathy (DCM) with biventricular and biatrial involvement.
- To correlate antemortem echocardiographic findings with postmortem pathological and immunohistochemical results.
- To contribute to the understanding of DCM in cats, a condition rarely observed.
Main Methods:
- Echocardiography was performed to assess cardiac structure and function, revealing a dilated cardiomyopathy phenotype.
- Comprehensive diagnostic tests, including thoracic radiographs, blood work, and specific biomarker analysis, were conducted to rule out secondary causes.
- Postmortem examination included gross pathology, histopathology, and immunohistochemistry to evaluate myocardial structure and protein expression.
Main Results:
- Echocardiography showed biventricular dilation, biatrial dilatation, left atrial dysfunction with spontaneous echocontrast, and signs of right-sided congestive heart failure.
- Postmortem examination revealed myofiber thinning with a wavy appearance in the ventricles and adipose tissue replacement in the atria.
- Immunohistochemistry demonstrated abnormal expression of desmin, vimentin, and connexin 43 in the myocardium.
Conclusions:
- A diagnosis of feline dilated cardiomyopathy with biventricular and biatrial involvement was confirmed through extensive antemortem and postmortem investigations.
- The pathological findings closely resembled those seen in canine and human DCM, including the attenuated wavy fiber pattern.
- This case highlights the importance of considering DCM in cats presenting with specific echocardiographic findings, despite its rarity.
Abstract:
An 8-year-old castrated male Exotic Shorthair cat was referred due to the onset of abdominal effusion. Echocardiography revealed a dilated cardiomyopathy phenotype affecting both ventricles, associated with biatrial dilatation, left atrial dysfunction with spontaneous echocontrast, and right-sided congestive heart failure. Additional diagnostic tests (thoracic radiographs, complete blood cell count, serum biochemistry, assessment of thyroid status, cardiac troponin I and plasma taurine concentrations, and urinalysis) ruled out secondary conditions able to cause a similar echocardiographic phenotype. Despite prompt initiation of cardiac therapy (furosemide, pimobendan, clopidogrel, and rivaroxaban) and subsequent hospitalization for further medical support, the cat's clinical condition deteriorated, ultimately leading to euthanasia. Postmortem examination revealed extensive areas of myofiber thinning with a wavy appearance in both ventricles, closely resembling the attenuated wavy fiber pattern described in dogs affected by dilated cardiomyopathy. Additionally, multifocal replacement of myofibers by adipose tissue was found in both atria. Immunohistochemical analysis showed abnormal expression patterns of desmin, vimentin, and connexin 43, similar to those previously reported in humans and dogs with dilated cardiomyopathy. Given the thorough antemortem and postmortem investigations and the associated findings, a rare case of feline dilated cardiomyopathy with biventricular and biatrial involvement was diagnosed.
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