Friday, August 15, 2014

Polycythemia Vera




Polycythemia vera is a disease in which too many red blood cells are made in the bone marrow.
In polycythemia vera, the blood becomes thickened with too many red blood cells. The number of white blood cells and platelets may also increase. These extra blood cells may collect in the spleen and cause it to swell. The increased number of red blood cells, white blood cells, or platelets in the blood can cause bleeding problems and make clots form in blood vessels. This can increase the risk of strokeor heart attack. In patients who are older than 65 years or who have a history of blood clots, the risk of stroke or heart attack is higher. Patients also have an increased risk of acute myeloid leukemia orprimary myelofibrosis.
Possible signs of polycythemia vera include headaches and a feeling of fullness below the ribs on the left side.
Polycythemia vera often does not cause early symptoms. It is sometimes found during a routine blood test. Symptoms may occur as the number of blood cells increases. Other conditions may cause the same symptoms. Check with your doctor if you have any of the following problems:
  • A feeling of pressure or fullness below the ribs on the left side.
  • Headaches.
  • Double vision or seeing dark or blind spots that come and go.
  • Itching all over the body, especially after being in warm or hot water.
  • Reddened face that looks like a blush or sunburn.
  • Weakness.
  • Dizziness.
  • Weight loss for no known reason.
Special blood tests are used to diagnose polycythemia vera.

In addition to a complete blood countbone marrow aspiration and biopsy, and cytogenetic analysis, aserum erythropoietin test is used to diagnose polycythemia vera. In this test, a sample of blood is checked for the level of erythropoietin (a hormone that stimulates new red blood cells to be made


Primary myelofibrosis is a disease in which abnormal blood cells and fibers build up inside the bone marrow.
The bone marrow is made of tissues that make blood cells (red blood cellswhite blood cells, andplatelets) and a web of fibers that support the blood-forming tissues. In primary myelofibrosis (also called chronic idiopathic myelofibrosis), large numbers of blood stem cells become blood cells that do not mature properly (blasts). The web of fibers inside the bone marrow also becomes very thick (likescar tissue) and slows the blood-forming tissue’s ability to make blood cells. This causes the blood-forming tissues to make fewer and fewer blood cells. In order to make up for the low number of blood cells made in the bone marrow, the liver and spleen begin to make the blood cells.
Possible signs of primary myelofibrosis include pain below the ribs on the left side and feeling very tired.
Primary myelofibrosis often does not cause early symptoms. It is sometimes found during a routineblood test. The following symptoms may be caused by primary myelofibrosis or by other conditions. Check with your doctor if you have any of the following problems:
  • Feeling pain or fullness below the ribs on the left side.
  • Feeling full sooner than normal when eating.
  • Feeling very tired.
  • Shortness of breath.
  • Easy bruising or bleeding.
  • Petechiae (flat, red, pinpoint spots under the skin that are caused by bleeding).
  • Fever.
  • Night sweats.
  • Weight loss.
Certain factors affect prognosis (chance of recovery) and treatment options for primary myelofibrosis.
Prognosis (chance of recovery) depends on the following:

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