The post What Is Bone Marrow? We Dig In on This Efficient Producer of Stem Cells appeared first on University Health News.
]]>Our bone marrow produces stem cells that mature into red blood cells (200 billion every day), white blood cells (up to 100 billion), and platelets (400 billion). Below, we’ll delve into each, describing their role and what can go wrong, along with symptoms and treatment. (Also, click here to read our post When Do You Need a Bone Marrow Test?)
Bone marrow produces stem cells that can become red blood cells, whose job is to distribute oxygen and carbon dioxide to the body’s cells, tissues, and organs. They have a life expectancy of between 100 and 120 days, and they become less active and more fragile with age. About 1 percent of the body’s red blood cells are removed every day by a type of white blood cell.
Condition | Treatment |
Iron deficiency | Iron supplements |
Pernicious anemia | High-dose B12 supplements |
Aplastic anemia | Transfusions, bone marrow transplant |
Autoimmune hemolytic anemia | Immune suppressants (e.g., prednisone) |
Sickle cell anemia | Blood transfusions, pain meds, bone marrow transplant |
Five different kinds of white blood cells are produced by bone marrow to fight infections and outside forces like smoke and dust. When you have an infection, the number of white blood cells increases significantly. White blood cells make up only 1 percent of our blood, and a drop of blood contains between 7,000 and 25,000 white blood cells. Think of them as your bodyguards who have a lifespan of only one to three days.
Condition | Treatment |
Acute myeloid leukemia | Chemotherapy, targeted drug therapy, stem cell transplant |
Chronic lymphoid leukemia | Chemotherapy, rituximab, bendamustine, ibrutinib, alemtuzumab with rituximab |
Chronic myelomonocyctic leukemia | Azacytidine, decitabine, hydroxyurea, stem cell transplant, transfusions, antibiotics |
We need platelets to help blood clot and stop bleeding. A normal platelet count is 150,000 to 450,000 per microliter of blood. The risk for spontaneous bleeding develops if a platelet count falls below 10,000 to 20,000. Each platelet has a lifespan of seven days. When a blood vessel is damaged, it sends a message that is picked up by platelets, which rush to the affected area and repair it.
In some cases, the problem is simply platelet dysfunction. It is caused by diseases (kidney disease, Lupus, multiple myeloma), infection, or certain drugs (aspirin, NSAIDS, other antiplatelet medications).
Condition | Treatment |
Thrombocytopenia | Change in medications, blood/platelet transfusions, corticosteroids, splenectomy |
Thrombocythemia | Observation, hydroxyurea, anagrelide, interferon |
Thrombocytosis | Low-dose aspirin, hydroxyurea, anagrelide, interferon, plateletpherisis |
Multiple myeloma occurs in plasma cells that originate in bone marrow. They make antibodies that guard against bacteria. People who have multiple myeloma have plasma cells that don’t reproduce normally. Instead, they become cancerous, divide, and grow out of control, often appearing in several places in the body. The cause is unknown. Bone damage is the primary effect of the disease.
Multiple myeloma is treated by chemotherapy, stem cell transplant, radiation, and surgery.
BONE MARROW TRANSPLANTS
A bone marrow transplant, also called a stem cell transplant, might be used to treat diseases such as leukemia, anemia, multiple myeloma, lymphoma, and immune deficiencies. It can come from the patient or from a donor. It can replace diseased bone marrow or help re-start the immune system, and it can come from bone marrow, blood vessels, and umbilical cord blood collected after birth.
Although life-saving and safe for some, bone marrow transplants carry serious and perhaps fatal risks for others.
Lymphomas are cancer cells in the lymphatic system that can develop in multiple locations, including in bone marrow. You’ll recognize them by their names—non-Hodgkin lymphoma and Hodgkin lymphoma. Both affect white blood cells, the only difference being a specific type of cell present in Hodgkin’s lymphoma.
Lymphomas are not preventable, but survival rates with treatment are good. It includes biologic therapy (drugs that trigger the immune system to attack cancer cells), antibody therapy (to counteract antigens), chemotherapy and radiation (to kill cells), steroids, and surgery.
Bone marrow is life-giving and essential, but also vulnerable and at times malfunctioning. Getting regularly scheduled physical exams that include blood tests is the best way to guard against and get early treatment for bone marrow disorders.
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]]>The post Leukemia Symptoms: Know the Signs appeared first on University Health News.
]]>In general terms, leukemia is cancer of your body’s blood-forming tissues, such as the bone marrow. Signs of leukemia vary, depending on the type of cancer you have; in some cases, leukemia causes no symptoms early on.
Since many leukemia symptoms are vague and may be caused by other conditions—cancerous and non-cancerous—it’s important to have them evaluated by your physician. A prompt, accurate diagnosis means an earlier start to treatment that may save your life.
Leukemia results in overproduction of cancerous white blood cells that don’t function properly. Eventually, leukemia cells crowd out and inhibit the formation of normal red blood cells, platelets, and healthy white blood cells, which fight infection.
Acute forms of leukemia include two main subtypes: acute lymphocytic leukemia and acute myeloid leukemia. The acute forms progress more rapidly and, left untreated, can result in death in weeks or months. However, some acute leukemias may respond more favorably to treatment and, in many cases, can be cured.
Chronic leukemias tend to advance more slowly and may not cause problems until later stages—oftentimes, patients can live for many years—but they tend to be more difficult to cure than acute forms. The two main subtypes are chronic lymphocytic leukemia and chronic myeloid leukemia.
Leukemia symptoms vary depending on whether you have an acute or chronic form of the disease. Early acute leukemia symptoms may resemble those of the flu, and include fever, achy joints, fatigue, and swollen lymph glands.
As acute leukemia progresses and platelet production wanes, clotting problems may develop, causing easier bruising or bleeding, or the formation of tiny red spots on the skin known as petechiae. Declines in healthy white blood cells may reduce your ability to fight infections.
Many people with chronic leukemias, particularly those in the early stages, have no symptoms and are diagnosed incidentally on the basis of an elevated white blood cell count on blood tests performed for another reason. Chronic lymphocytic leukemia symptoms include fever, dizziness, fatigue, infections, excessive sweating, night sweats, swollen lymph glands, loss of appetite and related weight loss, and excessive bruising and bleeding.
Chronic myeloid leukemia symptoms include fever, fatigue, night sweats, weight loss, and bone pain. Also, patients with either form of chronic leukemia may develop a sense of fullness in the belly, even after eating little food, as well as pain or pressure in the upper left side of the abdomen caused by an enlarged spleen.
Your physician will review your medical history, perform a physical exam to look for leukemia symptoms, and order blood tests to measure levels of white blood cells and platelets. If the test results are abnormal, your doctor may recommend a bone marrow biopsy to help identify the type of leukemia you have and to guide treatment decisions. In some cases, a lumbar puncture may be necessary to determine if leukemia cells have spread to the cerebrospinal fluid, which nourishes the spinal cord and brain.
All people with chronic myeloid leukemia and about one-quarter of adults with acute lymphocytic leukemia have a genetic abnormality known as BCR-ABL, which leads to production of a protein that promotes cancer growth. As such, if testing reveals that you have one of these forms of leukemia, your doctor will probably order genetic testing to identify BCR-ABL. This testing is important because your physician can prescribe treatments that specifically target BCR-ABL and its related protein.
Originally published in 2016, this post is regularly updated.
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