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aplastic anemia
(redirected from Bone marrow aplasia)

   Also found in: Dictionary/thesaurus, Medical, Wikipedia 0.03 sec.

aplastic anemia

 or anemia of bone-marrow failure

Inadequate blood-cell formation by bone marrow. Pancytopenia is the lack of all blood-cell types (erythrocytes, leukocytes, and platelets), but any combination may be missing. Drug, chemical, or radiation exposure most often causes the disease, but about half of all cases have no known cause. It may occur at any age. Acute disease may be quickly severe, even fatal; chronic disease has symptoms including weakness, shortness of breath, headache, fever, and pounding heart. There is usually a waxy pallor. Hemorrhages occur in mucous membranes, skin, and other organs. Lack of white blood cells lowers resistance to infection and becomes the major cause of death. Very low platelet count may lead to severe bleeding. The treatment of choice is bone-marrow transplantation. Otherwise treatment involves avoiding any known toxic agent and giving fluids, glucose, and proteins (often intravenously) as well as blood components and antibiotics.


aplastic anemia [ā′plas·tik ə′nēm·yə]
(medicine)
A blood disorder in which lymphocytes predominate while there is a deficiency of erythrocytes, hemoglobin, and granulocytes.


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The man claimed that doctors went through a series of tests on the child knowing quite well that it was a waste of time since he didn't suffer from bone marrow aplasia.
Within a few days, the patient's symptoms decreased, and she was discharged from hospital on day 41, despite ongoing bone marrow aplasia with antimicrobial and antimycotic prophylaxis, including trimethoprim/ sulfamethoxazole (160 mg/800 mg once daily) and (voriconazole 200 mg twice daily).
The man claimed that doctors went through a series of tests on the child knowing quite well that it was a waste of time since he didn't suffer from bone marrow aplasia.
 
 
 
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