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Aplastic Anemia

Aplastic Anemia – General Information

Aplastic Anemia is an infrequent illness which is described as a nonaccomplishment of the bone connective tissue to produce enough cells in order to assure a normal circulation. This disorder is neither inherited nor acquired at birth, but it appears during the patient’s life and it is known to be an autoimmune disorder.  In what concerns a morphologic evaluation, the bone connective tissue is composed of hematopoietic substances, which tend to become unresponsive at some point and cause this particular disease. Aplastic Anemia affects a small number of people: there were reported about 4 or 5 cases in a million people. The difference between Europe and the USA is not even noticeable, but a higher rate can be observed in poorer countries and areas, such as Thailand and Bangkok. The most cases are known to develop in Japan, about 20 cases in one million people. From this data, we can assume that the evolution and the appearance of the disease depends on the environmental factors and natural conditions of life, such as a high exposure to toxic products and substances. Aplastic Anemia can even lead to death; this may happen if the patient does not benefit of any kind of treatment and if he develops some other major problems, like infections or severe bleeding. However, the mortality rate is significantly minor in contrast with other medical problems. There are no certain results in what concerns those who are more likely to develop the disease: the race or the sex of the sufferers does not change the possibility to experience such a disease.

Aplastic Anemia – Symptoms

The symptoms and signs of Aplastic Anemia are totally connected to the level of the deficiency of the blood cells. The most severe problem which can appear is the blood cancer, but there are also other symptoms which can develop, depending on which of the cells are insufficient. This way, if there appears an insufficiency of the red blood cells, the symptoms which develop are:
  • Tiredness
  • Shortness of breath
  • Fatigue
  • Paleness
  • Beating noise in the ears
  • Headaches
  • If there is an insufficiency of white blood cells, the patient can experience the following problems:
  • Infections, located in the chest or skin
  • Persistent or recurrent sore throat
  • In other cases, there can appear an insufficiency of platelets, which is characterized by:
  • Gum bleeding
  • Prolonged periods
  • Nose bleed
  • Skin infection
  • Prominent red spots on the legs
  • Blood assaults in the mouth
The clinical manifestations of those who suffer from Aplastic Anemia start with insidious problems, which consist of bleeding, development of infections in certain areas and high fever. Physical examination can display other signs of this disease, like tachycardia, pallor or thrombocytopenia. A small number of patients can experience jaundice or hepatitis.  After the doctor diagnoses the patient with this disease, he must be informed about the medical history of the sufferer; he must also look for certain evident problems, such as short stature, skin pigmentation, mental retardation, microcephaly, skeletal abnormalities. Furthermore, he should examine the hands and the nails for evidence of dyskeratosis congenita.

Aplastic Anemia – Treatment

If you are suspect of developing Aplastic Anemia, your doctor may recommend you to take one of the following tests:

  • Blood cell testing, especially in order to determine the level of hemoglobin and red cells
  • Biochemical profile: a Coombs test, determination of the level of bilirubin, lactic dehydrogenase, transaminase and an analysis of the kidney functionality
  • Serologic tests for viral agents, such as HIV
  • An autoimmune- disorder evaluation
  • The Ham test
  • Histo-compatibility tests, conducted in order to establish potential donors, especially in the case of young sufferers.
  • Diepoxubutane incubation.
  • All these examinations must be performed as soon as possible, as the patient’s life depends on them; furthermore, after he receives the results, the doctor should rapidly choose the best way of treating the patient. The medical care available for the sufferers of Aplastic Anemia consists of:

Transfusions: this is the first action when a person is diagnosed with this disease; the transfusion will establish the patient’s condition and will keep him in a normal condition until other measures will be taken. The transfusion should be made from others than relatives, as in the case of family members the antigens may interfere and cause more serious problems. If the transfusion is not vital, the doctor should consult with a specialist in Aplastic Anemia before choosing such a procedure.

Treatment of infections: must be made quickly, as the infections can result into death. The risk agents include indwelling catheters, prolonged neutropenia and fungal infections. The most common treatment for infections is the administration of antibiotics and, in special conditions, the administration of antifungal agents, especially in what concerns the patients who experience high and persistent fever. Furthermore, the doctor should find an appropriate donor and he must assure that there will be no side effects.

Immunosuppressive therapy: this procedure is needed if no appropriate donor was found or if the sufferer is an old person. The response of such intervention is though quite slow and the patient will need permanent observation for at least two months. In most of the cases, the patients observe an improvement and, within a year, they can renounce at transfusions. The negative part is the fact that most often there appear relapses and the sufferers need another intervention. The studies show that, in some cases, a higher dosage can prove more effective and it can assure long-term benefits; however, the doctors do not recommend such a treatment. In what concerns surgical care for Aplastic Anemia, all the patients need a venous catheter before any therapy is administrated.

Other medications may be prescribed by your personal doctor, depending on your response to therapy and medical interventions. All the patients should be treated by a specialized person; if that is not possible; than they must assure that their doctor consults permanently an expert. Even if a patient receives the appropriate care for Aplastic Anemia, there can appear some complications, such as: bleeding, minor infections or graft failure. In order to prevent such complications, the patients should maintain their personal hygiene.


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