AL Amyloidosis

What is AL Amyloidosis?

AL Amyloidosis (also called “primary” amyloidosis) is a blood illness in which a special protein builds up in various parts of the body. This protein, called “M-protein,” is actually made up of pieces from immunoglobulins (also called antibodies) which are naturally in the body and fight off infection. In the case of people with amyloidosis, too many of these disease fighting  pieces are present in blood flow. They can get stuck in almost any organ in the body, such as the brain, the lungs, the liver, the heart, the skin, or the kidneys. As these proteins  build up, they begin to get in the way of the job of whichever organ they are in. Although AL amyloidosis can be assumed  from many of its different symptoms (see below), the only way to know for sure that it is there is to analyze the cells with a biopsy.

Kidney, amyloidosis happens when the irregular proteins described above began to get stuck in in the kidneys.  As the amyloid builds up, the kidneys are no longer able to work properly. The kidneys normally filter and clean the blood, getting rid of the body’s natural waste products as urine. If they are unable to do this, these waste products build up in the blood. This is called kidney failure. Eventually kidney failure can also cause problems with low red blood cell count, high blood pressure, and fluid buildup.

What does it look like?

First, a quick look at the kidney- most people have two kidneys, one on each side of their lower back. All of the blood in your body passes through your kidneys many times during the day, and each time blood goes through some of it gets cleaned by the glomeruli (just one= glomerulus).

This filtering is how your body gets impurities out of  the blood (and removes extra water), and some of the cleaned blood becomes your urine. Urine isn’t red (like blood) because the red blood cells, which give blood its color, are too big to fit through the filters. A glomerulus is just a tiny bag of blood containers through which blood gets filtered, and all of the clean blood (urine) runs into tubes (ureters) which eventually lead to your bladder.

In the affected filter on the right, almost all of these loops have flattened because of all the built up M-protein. Shown above are two glomeruli, or kidney filters, as they look under a microscope. The normal filter is on the left, and the filter damaged by this disease is on the right. See that in the normal filter, there are many open “loops” scattered throughout- these are all small blood vessels seen in a small piece cut from the kidney. 

Amyloidosis-Glom Stain

Shown above is another kidney filter (glomerulus). This time a “stain” has been added that turns the damaged cells bright green.

Amyloidosis-Congo Red

This is another stain that is used in finding disease, called “Congo Red”. This stain turns “bright apple green” when it touches the sick cells.

Amyloidosis-LM and IM

How did I get it?

We don’t yet know why some people get AL amyloidosis, even though 1,000-3,000 new cases are found each year in the US.  About 2/3 of these patients are male, and almost all of them are over the age of 40. Although this type of amyloidosis can occur by itself, it often happens with other blood disorders, such as multiple myeloma and Waldenstrom’s Macroglobulinemia. Both of these are diseases of the type of blood cells that produce antibodies.

What are the symptoms?

Amyloidosis can harm many organs other than the kidney, and its symptoms can therefore be very different.  Some of the most common are listed below, along with the organs involved.

KidneyKidney failure, fluid retention, swelling, shortness of breath
Heart Heart failure, arrhythmias, heart attack
Gastrointestinal Liver/spleen swelling, GI bleeding, malabsorption
Neurologic Pain and numbness
Musculoskeletal Swollen (but weakened) muscles, swollen tongue, joint pain
Blood Bleeding, anemia
Lung Shortness of breath, fluid in the lung
Skin Thickened skin, easy bruising

Amyloidosis can be determined from any of the problems listed above. Both the blood and the urine can also be tested for the M-protein that causes this disorder. However, an actual diagnosis requires a sample of an effected organ. Although this can be any  organ, such as skin or bone marrow, this disease can only be diagnosed by looking at a piece of your kidney.

What are my options for treatment?

Because AL amyloidosis is caused by too many antibodies, which come from blood cells, it is best treated by a doctor who looks at blood and blood cancers (Hematologist/Oncologist). Treatment usually includes some sort of chemotherapy; some of the most common drugs used are- Steroids, Melphalan, and Thalidomide. Sometimes a bone marrow transplant is needed as well.

What are my chances of getting better?

Because primary amyloidosis can affect so many different organs, what it does in the body varies widely from person to person.  The most life threatening problems are usually not in the kidney, but rather with heart problems or infection. Patients most at risk have one or more of the following: 

  • High numbers of circulating plasma cells
  • Significant bone marrow infiltration
  • Heart involvement

Patients that respond to therapy usually have stabilization of their kidney disease as well. When they do not, kidney replacement therapy (dialysis) may become necessary.