Amyloidosis Symptoms

Amyloidosis Symptoms And Treatment

Our today topic is amyloidosis symptoms and treatment.What is amyloidosis?What are the causes of it?What are the symptoms and treatments?

What is Amyloidosis?
Amyloidosis is a specific protein called amyloid that accumulates in the organs in excess, causing these organs to become normally inoperable.
Amyloidosis can affect the heart, kidneys, liver, spleen, nervous system, menses and intestines. Although this is a rare disease, it can be fatal. (For example, it affects 4,000 people per year in the USA.)

Amyloidosis can sometimes develop in certain types of cancer, such as multiple myeloma, Hodgkin’s disease, and people suffering from diseases such as the Mediterranean flare (an intestinal disease). Sometimes it can be seen in kidney patients who have been on dialysis for a long time.

Amyloidosis Symptoms And Treatment

There are 3 types of amyloidosis :

Primary Amyloidosis

The most common type of amyloidosis. It has no link to any disease and can affect the heart, lungs, skin, tongue, nerves and intestines.

Secondary Amyloidosis

It is a type of amyloidosis that is associated with chronic diseases such as tuberculosis, rheumatoid arthritis and bone marrow inflammation. It usually affects the kidneys, the spleen, the liver and the intestines.

Hereditary Amyloidosis

It’s amyloidosis that passes through family members. It affects the digestive system with the nervous system.

Amyloidosis Symptoms And Treatment

Amyloidosis Symptoms
The symptoms vary from patient to patient depending on the organ affected by the disease. Some people may not even see the symptoms, which makes diagnosis difficult.

Symptoms can hide themselves when amyloidosis is linked to another disease. The following diseases can be fatal before amyloidosis is found.

These are :

Growing liver
Greater language
Irregular heartbeats
Diarrhea and constipation
Swallowing difficulty
Feeling of fainting and fainting
Weight loss
Numbness in hands and feet
Severe fatigue
Shortness of breath
Deride changes
Swelling of legs and wrists
Amyloidosis depends on the organ that affects the severity. Kidney and heart effects can be fatal.

– When the amyloidosis occurs in the kidneys, the kidneys have the ability to shed blood and the proteins are confused.

– The first symptom of amyloidosis is shortness of breath, and the blood pump level in the advanced level may be impaired.

Amyloidosis Symptoms And Treatment

Other indications of amyloidosis include :

– Burning sensation due to irritation of nerves by amyloid

– Carpal tunnel syndrome causing numbness in the fingers

– Disturbances in the nervous system

– Feeling numb or numb on the toes

– weakness in the limb when the amyloid does not destroy the nerves

Causes of Amyloidosis and Risk Factors
The reason for the production and accumulation of amyloid in tissues is unknown. A person’s amyloidosis is not related to the risk of getting caught (including proteins) or lifestyle or amount of stress.

The disease starts at bone marrow. Bone marrow produces red and white blood cells, clotting cells, and antibodies that protect against body infections. The body breaks them up after they see the antibodies work. amyloidosis occurs when the bone marrow cells produce antibodies that can not be broken down. Antibodies proliferate and eventually accumulate as amyloid in the tissues.

Amyloidosis Symptoms And Treatment

The risk of amyloidosis is higher in people with :

People over 50 years
In those with chronic infection or inflammatory diseases
In family history of amyloidosis
In multiple myeloma cases. Amyloidosis occurs in 10-15% of multiple myeloma patients.
It’s kidney disease and it’s been on dialysis for over 5 years

Diagnosis of Amyloidosis
Blood and urine tests can reveal abnormal protein in the body, but the precise way to diagnose amyloidosis is to do tissue sample analysis at the microscope. Tissue is usually extracted from abdominal fat or rectum. In addition, tissue samples can be taken from the nerves, liver, kidneys and gums. Samples are spotted with a dye entering the amyloid reaction and the results are analyzed on a microscope.

Treatment of Amyloidosis
There is no cure for amyloidosis. If there is a disease that causes amyloidosis, the treatment is aimed at healing this disease so that the amyloidosis is expected to stay in the middle.

Some of the drug types used for amyloidosis are:

– Corticosteroids that prevent inflammation (swelling and tenderness)
– Pain killers

The effects of many drugs on amyloidosis are being investigated. (including drugs used for multiple myeloma)

Amyloidosis Symptoms And Treatment

– A nutritionally rich eating habit satisfies the body’s energy needs adequately. Good nutrition helps to treat many complications that may arise from amyloidosis. Special diets can be passed on to be indicated and depending on which organs the disease affects. For example, if the kidneys are affected, the doctor may recommend less salty diets or diuretics.

– The purpose in secondary amyloidosis is to treat the cause of the disease.

– Amyloidosis can also be caused by kidney transplantation when it affects the kidneys. Dialysis can also be helpful. But amyloid is eventually found in the kidney. Research is also underway to determine whether stem cell embryos can be used to treat affected organs from amyloidosis.

– Amyloidosis can also be done with heart transplantation, which affects the heart. People with amyloid heart disease should be cautious if they are picking up thistle because it can trigger irregular heartbeats. Myocardial amyloidosis is the most common cause of death. This is usually due to irregular heartbeats or heart failure that can not be rectified.

– In some cases of hereditary amyloidosis, kidney transplantation may be beneficial because it allows the mutant protein to get rid of it.

– Amyloidosis is under investigation to find new treatments. One of these is for stem cell transplantation involving the replacement of diseased or destroyed bone marrow using chemotherapy and transplantation of immature blood cells. Cells can be collected from the patient’s own body or from a donor.

Graves’ Disease

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