Related Experiment Video
Updated: Jun 27, 2026

10:21
Scanning Electron Microscopy of Macerated Tissue to Visualize the Extracellular Matrix
Published on: June 14, 2016
Endomyocardial fibrosis and restrictive cardiomyopathy: pathologic and clinical features
Summary
Restrictive cardiomyopathy (RCM) in cats is poorly defined, often presenting as endomyocardial fibrosis. This condition causes severe scarring, potentially reducing heart chamber volume and leading to diastolic dysfunction.
Area of Science:
- Veterinary Cardiology
- Cardiovascular Pathology
Background:
- Restrictive cardiomyopathy (RCM) is a primary myocardial disorder known for diastolic dysfunction and diverse presentations.
- Clinicopathologic features of RCM in feline species are not well-established.
- A specific form of RCM involves endomyocardial fibrosis.
Purpose of the Study:
- To define the clinicopathologic features of restrictive cardiomyopathy (RCM) in cats.
- To characterize the pathological findings associated with endomyocardial fibrosis in feline RCM.
Main Methods:
- Review of clinicopathologic and histopathologic data from feline cases of restrictive cardiomyopathy.
- Detailed examination of endocardial and myocardial tissues for fibrosis and scarring.
Main Results:
- Endomyocardial fibrosis is a hallmark of feline RCM, characterized by severe endocardial scarring.
- Lesions may diffusely affect the left ventricle or form distinct scars, potentially reducing chamber volume and causing stenosis.
- Severe left atrial enlargement and variable ventricular hypertrophy are common findings.
Conclusions:
- Feline restrictive cardiomyopathy associated with endomyocardial fibrosis presents with distinct clinicopathologic and histopathologic features.
- The condition is characterized by significant endocardial scarring, left atrial enlargement, and potential hemodynamic compromise.
Related Concept Videos
Cardiomyopathy IV: Restrictive Cardiomyopathy
Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...
Myocarditis I: Introduction
Myocarditis is inflammation of the myocardium, which is the muscular layer of the heart.EtiologyMyocarditis has a diverse etiology, including a wide range of infectious and non-infectious causes:Infectious CausesViral: Common viruses include Coxsackie A and B, adenovirus, parvovirus B19, enteroviruses, and influenza A.Bacterial: Examples include infections caused by Streptococcus, Staphylococcus, and Mycoplasma species.Rickettsial: Infections like Rocky Mountain spotted fever can result in...
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Cardiomyopathy II: Dilated Cardiomyopathy
Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
Myocarditis II: Clinical Features and Diagnostic Tests
Myocarditis is an inflammation of the heart muscle. The symptoms vary widely, encompassing asymptomatic presentations to severe, acute manifestations.Clinical PresentationAsymptomatic cases: In some instances, myocarditis may be asymptomatic, with the infection resolving without intervention. These cases often go undetected unless discovered incidentally through diagnostic imaging or tests conducted for other reasons.General Early Symptoms: Early symptoms of myocarditis are non-specific and can...

