Blood Dieseases
Blood disorders can affect any of the three
main components of blood:
- Red blood cells, which carry oxygen to the body's tissues
- White blood cells, which fight infections
- Platelets, which help blood to clot
Blood disorders can also affect the liquid portion
of blood, called plasma.
Recommended Related to Blood Disorders
Understanding Hemophilia -- the Basics
Hemophilia refers to a group of inherited disorders
that cause abnormal bleeding. The bleeding occurs because part of the blood --
called plasma -- has too little of a protein that helps blood clot. Symptoms of
hemophilia range from increased bleeding after trauma, injury, or surgery to
sudden bleeding with no apparent cause. There are two types of hemophilia:
Hemophilia A -- also called classic hemophilia -- is most common and occurs in
about 85% of people with hemophilia. Hemophilia B...
Treatments and prognosis for blood diseases vary,
depending on the blood condition and its severity.
Blood Disorders Affecting
Red Blood Cells
Blood disorders that affect red blood cells include:
Anemia : People with
anemia have a low number of red blood cells. Mild anemia often causes no
symptoms. More severe anemia can cause fatigue, pale skin, and
shortness of breath with exertion.
Iron-deficiency anemia: Iron is
necessary for the body to make red blood cells. Low iron intake and loss of
blood due to menstruation are the most common causes of iron-deficiency
anemia. Treatment includes iron pills, or rarely, blood transfusion.
Anemia of chronic disease: People
with chronic kidney disease or other chronic diseases tend to develop
anemia. Anemia of chronic disease does not usually require treatment.
Injections of a synthetic hormone (Epogen, Procrit) to stimulate the
production of blood cells or blood transfusions may be necessary in some people
with this form of anemia.
Pernicious anemia (B12 deficiency): An
autoimmune condition that prevents the body from absorbing enough B12 in the
diet. Besides anemia, nerve damage(neuropathy) can eventually result. High
doses of B12 prevent long-term problems.
Aplastic anemia: In people with
aplastic anemia, the bone marrow does not produce enough blood cells, including
red blood cells. A viral infection, drug side effect, or an autoimmune
condition can cause aplastic anemia. Blood transfusions, and even a bone marrow
transplant, may be required to treat aplastic anemia.
Autoimmune hemolytic anemia: In
people with this condition, an overactive immune system destroys the body's own
red blood cells, causing anemia. Medicines that suppress the immune system,
such as prednisone, may be required to stop the process.
Thalassemia: This is a genetic
form of anemia that mostly affects people of Mediterranean heritage. Most
people have no symptoms and require no treatment. Others may need regular blood
transfusions to relieve anemia symptoms.
Sickle cell anemia: A genetic
condition that affects mostly African-Americans. Periodically, red blood cells
change shape, and block blood flow. Severe pain and organ damage can occur.
Polycythemia vera : The body
produces too many blood cells, from an unknown cause. The excess red blood
cells usually create no problems but may cause blood clots in some
people.
Malaria: A mosquito's bite
transmits a parasite into a person's blood, where it infects red blood cells.
Periodically, the red blood cells rupture, causing fever, chills, and
organ damage. This blood infection is most common in Africa; those
traveling to Africa are at risk and should take preventive measures. Malaria
was eradicated from the U.S. in the 1940s.
Blood
disorders that affect white blood cells include:
Lymphoma : A form of blood cancer that
develops in the lymph system. In lymphoma, a white blood cell becomes
malignant, multiplying and spreading abnormally. Hodgkin's lymphoma and non-Hodgkin's
lymphoma are the two major groups of lymphoma. Treatment with chemotherapy and/or radiation can
extend life with lymphoma, and sometimes cure it.
Leukemia : A form of blood
cancer in which a white blood cell becomes malignant and multiplies inside bone
marrow. Leukemia may be acute (rapid and severe) or chronic (slowly
progressing). Chemotherapy and/or stem cell transplantation (bone
marrow transplant) can treat leukemia, and sometimes result in a cure.
Multiple myeloma: A blood cancer in
which a white blood cell called a plasma cell becomes malignant. The plasma
cells multiply and release damaging substances that eventually cause organ
damage. Multiple myeloma has no cure, but stem cell transplant and/or chemotherapy can
allow people to live for years with the condition.
Myelodysplastic syndrome: A
family of blood cancers that affect the bone marrow. Myelodysplastic syndrome
often progresses very slowly, but may suddenly transform into a severe
leukemia. Treatments usually include blood transfusions and chemotherapy. Stem
cell transplant can sometimes cure younger people with myelodysplastic
syndrome.
Blood Disorders Affecting Platelets
Blood disorders that affect the platelets include:
Thrombocytopenia : A
low number of platelets in the blood. Numerous conditions cause
thrombocytopenia; most do not result in abnormal bleeding.
Idiopathic thrombocytopenic
purpura: A condition causing a persistently low number
of platelets in the blood, due to an unknown cause. Usually there are no
symptoms, yet abnormal bruising, small red spots on the skin (petechiae), or
abnormal bleeding can result.
Heparin -induced
thrombocytopenia: A low platelet count caused by a reaction against
heparin, a blood thinner given to most people who are hospitalized to prevent
blood clots.
Thrombotic thrombocytopenic
purpura: A rare blood disorder causing small blood clots to
form in blood vessels throughout the body. Platelets are used up in the
process, causing a low platelet count.
Essential thrombocytosis (primary
thrombocythemia): The body produces too many platelets, due to an unknown
cause. The platelets do not work properly, resulting in excessive clotting,
bleeding, or both.
Blood Disorders Affecting Blood Plasma
Blood disorders that affect blood plasma include:
Sepsis : An
infection somewhere in the body spreads into the blood. Symptoms include fever,
rapid breathing, respiratory failure, and low blood pressure.
Hemophilia : A
genetic deficiency of certain proteins that help blood to clot. There are
multiple forms of hemophilia, ranging in severity from mild to
life-threatening.
von Willebrand disease: von
Willebrand factor is a protein in blood that helps blood to clot. In von
Willebrand disease, the body either produces too little of the protein, or
produces a protein that doesn't work well. The condition is inherited, but most
people with von Willebrand disease have no symptoms and don't know they have
it. Some people with von Willebrand disease will have excessive bleeding after
an injury or during surgery.
Hypercoaguable state
(hypercoagulable state): A tendency for the blood to
clot too easily. Most affected people have only a mild excess tendency to clot,
and may never be diagnosed. Some people develop repeated episodes of blood
clotting throughout life, requiring them to take a daily blood thinning medicine.
Deep venous thrombosis: A
blood clot in a deep vein, usually in the leg. A deep venous thrombosis can
dislodge and travel through the heart to the lungs, causing a
pulmonary embolism.
Disseminated intravascular
coagulation (DIC): A condition that causes tiny blood
clots and areas of bleeding throughout the body simultaneously. Severe
infections, surgery, or complications of pregnancy are conditions
that can lead to DIC.
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