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In This Topic
Blood Disorders
Anemia
Overview of Anemia
Causes
Symptoms and Diagnosis
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Chapters in Blood Disorders
  • Biology of Blood
  • Symptoms and Diagnosis of Blood Disorders
  • Blood Transfusion
  • Iron Overload
  • Anemia
  • Blood Clotting Process
  • Bleeding and Clotting Disorders
  • Bleeding Due to Abnormal Blood Vessels
  • Platelet Disorders
  • White Blood Cell Disorders
  • Plasma Cell Disorders
  • Leukemias
  • Lymphomas
  • Myeloproliferative Disorders
  • Spleen Disorders
Topics in Anemia
  • Overview of Anemia
  • Anemia Due to Excessive Bleeding
  • Iron Deficiency Anemia
  • Vitamin Deficiency Anemia
  • Anemia of Chronic Disease
  • Autoimmune Hemolytic Anemia
  • Sickle Cell Disease
  • Hemoglobin C, S-C, and E Diseases
  • Thalassemias
     
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    Overview of Anemia

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    Anemia is a condition in which the number of red blood cells or the amount of hemoglobin (the protein that carries oxygen in them) is low.

    Red blood cells contain hemoglobin, a protein that enables them to carry oxygen from the lungs and deliver it to all parts of the body. When the number of red blood cells is reduced or the amount of hemoglobin in them is low, the blood cannot carry an adequate supply of oxygen. An inadequate supply of oxygen in the tissues produces the symptoms of anemia.

    Causes

    The causes of anemia are numerous, but most can be grouped within three major mechanisms that produce anemia:

    • Blood loss (excessive bleeding)
    • Inadequate production of red blood cells
    • Excessive destruction of red blood cells

    Anemia may be caused by excessive bleeding. Bleeding may be sudden, as may occur in an injury or during surgery. Often, bleeding is gradual and repetitive, typically from abnormalities in the digestive or urinary tract or heavy menstrual periods. Chronic bleeding typically leads to low levels of iron, which leads to worsening anemia.

    Anemia may also result when the body does not produce enough red blood cells. Many nutrients are needed for red blood cell production. The most critical are iron, vitamin B12, and folate (folic acid), but the body also needs trace amounts of vitamin C, riboflavin, and copper, as well as a proper balance of hormones, especially erythropoietin (a hormone that stimulates red blood cell production). Without these nutrients and hormones, production of red blood cells is slow and inadequate, or the red blood cells may be deformed and unable to carry oxygen adequately. Chronic disease also may affect red blood cell production. In some circumstances, the bone marrow space may be invaded and replaced (for example, by leukemia, lymphoma, or metastatic cancer), resulting in decreased production of red blood cells.

    Anemia may also result when too many red blood cells are destroyed. Normally, red blood cells live about 120 days. Scavenger cells in the bone marrow, spleen, and liver detect and destroy red blood cells that are near or beyond their usual life span. If red blood cells are destroyed prematurely (hemolysis), the bone marrow tries to compensate by producing new cells faster. When destruction of red blood cells exceeds their production, hemolytic anemia results. Hemolytic anemia is relatively uncommon compared with the anemia caused by excessive bleeding and decreased red blood cell production.

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    Common Causes of Anemia

    Mechanism

    Examples

    Chronic excessive bleeding

    Bladder tumors

    Cancer in the digestive tract

    Heavy menstrual bleeding

    Hemorrhoids

    Kidney tumors

    Nosebleeds

    Polyps in the digestive tract

    Ulcers in the stomach or small intestine

    Sudden excessive bleeding

    Injuries

    Childbirth

    A ruptured blood vessel

    Surgery

    Decreased red blood cell production

    Aplastic anemia

    Chronic disorders

    Folate deficiency

    Iron deficiency

    Leukemia

    Lymphoma

    Metastatic cancer

    Myelodysplasia (abnormalities in bone marrow tissue)

    Myelofibrosis

    Multiple myeloma

    Vitamin B12 deficiency

    Vitamin C deficiency

    Increased red blood cell destruction

    Autoimmune reactions against red blood cells

    An enlarged spleen

    Glucose-6-phosphate dehydrogenase (G6PD) deficiency

    Hemoglobin C disease

    Hemoglobin E disease

    Hemoglobin S-C disease

    Hereditary elliptocytosis

    Hereditary spherocytosis

    Mechanical damage to red blood cells

    Paroxysmal nocturnal hemoglobinuria

    Sickle cell disease

    Thalassemia

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    More About Some Causes of Anemia

    Cause

    Mechanism

    Treatment

    Comments

    Enlarged spleen

    An enlarged spleen traps and destroys too many red blood cells.

    The disorder that caused the spleen to enlarge is treated.

    Sometimes the spleen must be removed surgically.

    Symptoms tend to be mild.

    Often, an enlarged spleen also traps platelets and white blood cells, thus reducing their number in the bloodstream.

    Mechanical damage to red blood cells

    Abnormalities in blood vessels (such as an aneurysm), an artificial or damaged heart valve, or extremely high blood pressure can break normal red blood cells apart.

    The cause of the damage is identified and corrected.

    The kidneys eventually filter the damaged red blood cells out of the blood but may be damaged by them.

    The spleen also filters the damaged red cells out of the blood.

    Paroxysmal nocturnal hemoglobinuria

    The immune system destroys red blood cells.

    Hemoglobin from these damaged cells is concentrated in urine during the night, resulting in dark, reddish urine in the morning.

    Corticosteroids and a new antibody drug, eculizumabSome Trade Names
    SOLIRIS
    , help relieve symptoms, but the only cure is allogeneic bone marrow transplantation.

    People with blood clots may need to take an anticoagulant.

    Bone marrow transplantation may be needed.

    People may have severe stomach cramps and clotting in the large veins of the abdomen and legs.

    Symptoms often occur in episodes (paroxysmally).

    Hereditary spherocytosis

    Red blood cells become misshapen and rigid, getting trapped and destroyed in the spleen.

    Treatment is usually not needed, but severe anemia may require removal of the spleen.

    This hereditary disorder can also cause bone abnormalities, such as a tower-shaped skull.

    Hereditary elliptocytosis

    Red blood cells are oval or elliptical in shape rather than the normal disk shape.

    Severe anemia may require removal of the spleen.

    The anemia is usually mild and requires no treatment.

    Glucose-6-phosphate dehydrogenase (G6PD) deficiency

    The G6PD enzyme is missing from red blood cell membranes.

    Without this enzyme, red blood cells are more likely to break apart when the person is stressed by triggers such as fever, infection, diabetic crisis, or certain drugs such as aspirinSome Trade Names
    BAYER
    and sulfa drugs.

    Anemia can be prevented by preventing or avoiding things that trigger it.

    This hereditary disorder almost always affects males.

    About 10% of black males and a smaller percentage of white people of Mediterranean origin have the disorder.

    Symptoms and Diagnosis

    Symptoms vary depending on the severity of the anemia and how rapidly it develops. Some people with mild anemia, particularly when it develops slowly, have no symptoms at all. Other people may experience symptoms only with physical exertion. More severe anemia may produce symptoms even when people are resting. Symptoms are more severe when mild or severe anemia develops rapidly, such as with bleeding that occurs when a blood vessel ruptures.

    Mild anemia often causes fatigue, weakness, and paleness. In addition to these symptoms, more severe anemia may produce faintness, dizziness, increased thirst, sweating, a weak and rapid pulse, and rapid breathing. Severe anemia may produce painful lower leg cramps during exercise, shortness of breath, and chest pain, especially if people already have impaired blood circulation in the legs or certain types of lung or heart disease.

    Sometimes anemia is detected before people notice symptoms, when routine blood tests are done.

    Low levels of hemoglobin and a low hematocrit (the percentage of red blood cells in the total blood volume) found in a blood sample confirm the anemia. Other tests, such as examining a blood sample under a microscope and less often examining a sample taken from the bone marrow, help determine the cause of the anemia.

    Spotlight on Aging

    Many disorders that cause anemia, especially cancer, tend to be more common among older people. Thus, many older people develop anemia. Iron deficiency anemia, usually due to abnormal bleeding, is the most common anemia among older people.

    Symptoms of anemia are basically the same in older people as in younger people. However, older people may not look pale. Also, even when anemia is mild, older people are more likely to become confused, depressed, agitated, or listless than younger people. They may also become unsteady and have difficulty walking. These problems can interfere with being able to live independently. However, some older people with mild anemia have no symptoms at all, particularly when anemia develops gradually, as it often does in older people.

    In older people, anemia caused by vitamin B12 deficiency may be mistaken for dementia because this type of anemia may affect the nerves and mental function.

    Having anemia may shorten the life expectancy of older people. Thus, identifying the cause and correcting it are particularly important.

    Last full review/revision June 2008 by Alan E. Lichtin, MD

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    Pronunciations

    aneurysm

    aplastic anemia

    corticosteroid

    dehydrogenase

    dementia

    elliptocytosis

    erythropoietin

    fibrosis

    glucose-6-phosphate dehydrogenase

    hematocrit

    hemoglobin

    hemolysis

    hemolytic

    hemolytic anemia

    lymphoma

    multiple myeloma

    myelofibrosis

    paroxysmal nocturnal hemoglobinuria

    polyp

    spherocytosis

    thalassemia

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    Next: Anemia Due to Excessive Bleeding

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