About loeffler fibroplastic parietal endocardi...

What is loeffler fibroplastic parietal endocardi...?

General Discussion

Endomyocardial fibrosis (EMF) is a progressive disease of unknown origin (idiopathic) that may seriously affect the heart. Its most obvious feature is a gross change in the makeup of the lining of the heart cavities (the endocardium) of one or both of the lower chambers of the heart (the ventricles) leading to the replacement of normal cells with fibrous tissue (fibrosis). This process is progressive and leads to the narrowing (constriction) of the right or left ventricular cavities. It may involve the valves between the chambers of the heart as well as the tendon-like cords that fix the valves to the ventricles (chordae tendineae). Loeffler's disease is a disease of the heart much like endomyocardial fibrosis. Some clinicians regard it as an early stage of EMF, although this idea remains controversial. Loeffler's disease is a rare disorder of unknown origin, characterized by abnormal increases in the number of particular white blood cells (eosinophilia), and like EMF, gross fibrosis of the endocardium, and inflammation of small blood vessels (arteritis).

What are the symptoms for loeffler fibroplastic parietal endocardi...?

Fever symptom was found in the loeffler fibroplastic parietal endocardi... condition

Wilhelm Loeffler initially described Loeffler's endocarditis in 1936, labeling it ""fibroplastic parietal endocarditis with blood eosinophilia.

  • Endocarditis parietalis fibroplastica is a rare, deadly disease with an unknown cause is a type of subendocardial mural fibrosis that worsens over time. It is linked to peripheral blood eosinophilia, occasionally of leukemoid proportions.
  • Loeffler's endocarditis is an unusual kind of limiting cardiomyopathy characterized by eosinophilia and endomyocardial fibrosis. It is most typically manifested as diastolic dysfunction or valvular anomalies resulting from eosinophilic infiltration and degranulation.
  • The clinical signs of Loeffler endocarditis generally reflect the numerous underlying illnesses that cause eosinophil dysfunction, as well as the significantly disparate rates of heart damage development.
  • Before cardiac problems are diagnosed, people may experience signs of a common cold, breathing problems, rhinitis, urticarial, or another allergy illness.
  • Cardiac symptoms include potentially fatal disorders, including cardiogenic shock or unexpected death caused by Irregular heartbeats.
  • Yet, the initial cardiac indications and symptoms of the condition are more typically the same as those found in other kinds of cardiomyopathy: Additional cardiac irregularities, signs of these arrhythmias like chest Palpitations, Dizziness, Lightheadedness, and Fainting; and symptoms of heart failure such as weariness, edema (Swelling) of the lower extremities, and breathlessness.
Symptoms
Common cold,Asthma,Rhinitis,Urticarial, or other allergic disorder, Chest Palpitations,Dizziness,Light headedness,Fainting
Conditions
Poor heart contractility,Irregular pulse and heart rate,Asthma,Rhinitis,Urticarial
Drugs
Diuretics,Digoxin,Angiotensin-converting enzyme (ACE) inhibitor angiotensin II receptor blockers,Beta-adrenergic blockers,Aldosterone antagonists

What are the causes for loeffler fibroplastic parietal endocardi...?

Variations in the KCNE1 and KCNQ1 genomes cause Jervell and Lange-Nielsen syndrome. These genes encode proteins that perform together to produce a route across cell membranes.

  • Positively charged potassium atoms ions are transported out of cells via these channels. The flow of potassium ions via these channels is essential for the regular operation of inner ear tissues and heart muscle.
  • KCNQ1 gene mutations cause around 90percent of the overall Jervell and Lange-Nielsen syndrome cases; KCNE1 gene mutations cause the remaining instances. Mutations in these genes disrupt the normal shape and function of potassium channels or restrict channels from forming.
  • These modifications affect the passage of potassium ions in the inner ear and cardiac muscle, resulting in hearing loss and the irregular heart rhythms associated with Jervell and Lange-Nielsen syndrome.
  • This disorder is transmitted in an autosomal recessive fashion, which means that both copies of the gene in each cell are mutated.
  • The parents of a kid with an autosomal recessive condition are usually unaffected but carry one copy of the faulty gene. Some KCNQ1 or KCNE1 mutant carriers have a long QT interval and concomitant heart problems, yet their hearing is normal.
Symptoms
Common cold,Asthma,Rhinitis,Urticarial, or other allergic disorder, Chest palpitations,Dizziness,Light headedness,Fainting
Conditions
Poor heart contractility,Irregular pulse and heart rate,Asthma,Rhinitis,Urticarial
Drugs
Diuretics,Digoxin,Angiotensin-converting enzyme (ACE) inhibitor angiotensin II receptor blockers,Beta-adrenergic blockers,Aldosterone antagonists

What are the treatments for loeffler fibroplastic parietal endocardi...?

Loeffler fibroplastic parietal endocarditis is a rare form of endocarditis, a condition where bacteria grow on the inner linings of your heart. The disease can cause serious complications, so it's important to know what treatments are available. Treatment for Loefler fibroplastic parietal endocarditis includes antibiotics and surgery. There are several different types of antibiotics you can use to treat this condition, but they all share one common goal: killing bacteria that may be in your body. They don't kill any other kind of cells in your body, so they're considered "targeted therapy." If your doctor thinks that surgery may be necessary because the infection has spread too far, they will recommend it as part of your treatment plan. In some cases, surgery may be needed if the infection has caused a hole or tear in one or more heart valves or if there is an abscess (an area where pus forms) on the heart wall or valve leaflets themselves. If you have undergone cardiac catheterization (inserting small tubes into blood vessels) during diagnosis or treatment for another condition such as coronary artery disease (CAD), then there is also an increased risk for developing endocarditis. The surgery can be done in one of two ways: 1. A heart valve transplant. This is done when the infection affects only one valve, and a new valve from another source can be used to replace it. 2. A homograft replacement procedure, which involves taking a healthy section of tissue from another part of your body and using it to patch up the damaged area on your heart. The symptoms of Loefler fibroplastic parietal endocarditis include: -Shortness of breath -Pressure in the chest -Irregular heartbeat (arrhythmia) -Fever

What are the risk factors for loeffler fibroplastic parietal endocardi...?

Loeffler fibroplastic parietal endocarditis is a rare disease that results from the accumulation of fibroblast-like cells in the parietal layer of the heart. The condition can be fatal if left untreated, but there are several risk factors that can increase your likelihood of developing this disease. The first risk factor for loeffler fibroplastic parietal endocarditis is being an older adult. People over 65 are at an increased risk because their immune systems become weaker with age, which makes them less able to fight off infection. They also have a higher chance of having had previous infections that can cause scarring of the heart valves, which increases your risk of developing loeffler fibroplastic parietal endocarditis. Another risk factor is having a history of rheumatic fever or rheumatic heart disease (RHD). RHD is an autoimmune disorder caused by streptococcal bacteria that infect your heart valves and create inflammation in those areas. This inflammation can lead to scarring and thickening of your heart valves, which increases your risk for developing loeffler fibroplastic parietal endocarditis later on in life. The risk factors for loeffler fibroplastic parietal endocarditis include: -Having a previous history of endocarditis (infection of the inner lining of the heart chambers or valves) -Having certain types of heart disease like mitral valve prolapse or rheumatic fever -Taking certain medications like steroids or anticoagulants -A history of intravenous drug use -Diabetes mellitus -Previous surgery on the heart

Is there a cure/medications for loeffler fibroplastic parietal endocardi...?

Restrictive cardiomyopathy, also known as fibroplastic parietal endocarditis with blood eosinophilia, is associated with impaired relaxation and diastolic filling of the heart.

  • Eosinophils infiltrate the endomyocardium in an abnormal infiltration, causing tissue damage from degranulation that ultimately results in fibrosis.
  • In other words, since the severity of initial eosinophilia directly correlates with the severity of acute myocarditis, patients with low to moderate levels of eosinophilia may only experience low-grade endomyocarditis that is not always clinically evident. However, this inflammation eventually still results in progressive fibrosis.
  • The patient is only diagnosed with fibrosis after developing symptoms. At this point, there are few options for management, and typically only two options left: Heart failure medications and Surgical intervention.
  • Due to mitral regurgitation, Loeffler endocarditis patients typically require mitral valve replacement.
  • A biological valve is preferred over a mechanical valve due to the high incidence of mechanical valve thrombosis. The mitral valve may be switched with a mechanical or biological prosthetic valve.
  • Since Loeffler endocarditis can be fatal, it must be diagnosed and treated immediately.
  • Individuals with a history of hypereosinophilia should be closely watched for the onset of thrombosis and fibrotic, restrictive cardiomyopathy.
  • Surgical intervention may be necessary to stop morbidity and mortality if the disease is discovered later in the disease process and fibrotic disease has already begun to develop.
  • Treatment with steroids and cytotoxic drugs can be helpful if the disease is discovered early.
Symptoms
Common cold,Asthma,Rhinitis,Urticarial, or other allergic disorder, Chest palpitations,Dizziness,Light headedness,Fainting
Conditions
Poor heart contractility,Irregular pulse and heart rate,Asthma,Rhinitis,Urticarial
Drugs
Diuretics,Digoxin,Angiotensin-converting enzyme (ACE) inhibitor angiotensin II receptor blockers,Beta-adrenergic blockers,Aldosterone antagonists

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