Multiple myeloma

Multiple myeloma is a disorder in which plasma cells are produced in an uncontrolled and invasive (malignant) fashion. Plasma cells develop from lymphocytes, a type of white blood cell. They are found primarily in the bone marrow and lymph nodes.

Plasma cells are responsible for helping the body fight infection. They produce antibodies that circulate in the blood and recognize markers, called antigens, on the cells of invading organisms like bacteria. These antibodies defend the body against foreign organisms.

Multiple myeloma occurs when the plasma cells in the bone marrow begin reproducing uncontrollably. While normal bone marrow contains less than 5% plasma cells, bone marrow in a patient with multiple myeloma contains over 10% plasmacells.

Multiple myeloma tends to be a disease of the elderly. The average patient is68 years old when diagnosed. During the last 10 years, doctors have seen anincrease in cases of multiple myeloma occurring at younger ages, but patientsare usually over age 40. Men have a slightly increased chance of having multiple myeloma, and African-Americans are twice as likely as Caucasians to develop the disease.

Although the exact cause of multiple myeloma has not been determined, researchers believe that it may be linked to exposure to certain environmental substances such as radiation and chemicals.

Bone pain is an extremely common symptom among patients with multiple myeloma. About 70% of all patients report bone pain as their first symptom. This pain is caused by plasma cells growing in number within the bone marrow, replacing normal marrow and putting pressure on the bone. Plasma cells also producechemicals called osteoclast activating factors (OAF). OAF encourage special cells called osteoclasts to break down bone. In healthy people this process isbalanced by the building up of new bone by cells called osteoblasts. In multiple myeloma, however, excess OAF are produced and bone is eaten away by overly active osteoclasts. Bones become weak (causing osteoporosis) and may break.

The antibodies that are over-produced in multiple myeloma function abnormally. Furthermore, other types of antibodies are under produced. Destruction of circulating antibodies also increases. This results in an increased chance ofdeveloping serious bacterial infections. The most common types of infectionsinclude pneumonia and kidney infections.

Abnormalities in the structure and function of kidney cells are extremely common in multiple myeloma. About half of all patients have kidney problems. These problems occur because of high levels of calcium in the blood (due to bonebreaking down), protein build-up, and increased circulating uric acid. Increased strain on the kidney to eliminate large amounts of the broken down products of antibodies and proteins may cause kidney damage or kidney failure.

Other problems are common in multiple myeloma. Because plasma cells take up space within the bone marrow, other cells normally produced there decrease andare sometimes defective in shape and function. Red blood cells decrease, resulting in anemia in about 80% of all people with multiple myeloma.

Circulating antibodies may interfere with clotting, resulting in an increasedrisk of bleeding. Abnormally thick blood may interfere with blood circulation anywhere in the body, but particularly in the fingers, toes, ears, and nose. Blood thickening may also cause headache, fatigue, and vision problems. Excess calcium in the blood may cause patients to feel weak, depressed, and confused. Sometimes, the plasma cells create a tumor called a plasmacytoma. Plasmacytomas may press on bone, causing fractures. Fractured bones may place unusual pressure on nearby nerves, resulting in nerve damage, pain, burning, tingling, and weakness of the affected muscle.

Diagnosis of multiple myeloma involves examination of blood, urine, bone marrow, and bones. Blood tests will reveal abnormalities, including anemia with abnormal red blood cells. Blood calcium will be high in about 33% of all patients. A specialized test called electrophoresis can be used to show an increased amount of antibodies in the blood and urine.

Examination of the bone marrow requires a test called a bone marrow aspiration. A long, thin needle is placed into the hip, and a sample of bone marrow iswithdrawn. In multiple myeloma, the bone marrow has a significantly increased percentage of plasma cells, usually well over 10%.

Because the treatments for multiple myeloma can be very damaging, and becausethe disease often progresses slowly, many patients are not treated until measurements of antibodies in the blood reach a particularly high level. Chemotherapy agents used in multiple myeloma include melphalan, cyclophosphamide, chlorambucil, and prednisone. These may be given over four to seven days in four to six week intervals. Chemotherapy may be given for several years. The disease usually recurs within a year after treatment has stopped. Chemotherapy can be given again, but each time the disease reappears it is less responsiveto treatment.

Bone pain is often treated with radiation directed at the problem area. Highblood levels of calcium may respond to treatment with prednisone. High bloodlevels of uric acid may improve with allopurinol. When anemia causes symptoms, blood transfusions may be necessary.

One general recommendation for alternative cancer treatment includes dietarysupplementation with beta-carotene, vitamin B6, vitamin C, vitaminE, selenium, and zinc as antioxidant protection. Other recommendations include reducing stress through techniques such as biofeedback training, guided imagery, and meditation. These same techniques are useful for pain relief.

About 15% of patients with multiple myeloma die within three months of diagnosis. About 60% of all patients respond to treatment and live for an average of two and a half to three years after diagnosis. About 23% of all patients die of other illnesses associated with advanced age.

User Contributions:

Hi - My mom-in-law survived this cancer for 10 yrs...she could have been still with us, had she taken the treatment properly. She did not get sciatica per se, but she had pain and numbness in her legs.
This is how her painkilers progressed:
Regular Tylenol or Advil-> Tylenol Arthirits-> Tylenol 3-> Oxycontin.

From my experience, I suggest start with one, monitor yourself for two days. If you are still in pain, go to next level and monitor. She was in hospital for a month just to figure out which medication in what quantity works for her,so that she is mobile, no pain and have better quality of life. And i have seen her fighting and adjusting herself to make work with those medications. The phase was tough on her, but she managed it pretty well. I wish you good luck. Take care.

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