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  2. Pancytopenia - Wikipedia

    en.wikipedia.org/wiki/Pancytopenia

    Pancytopenia is a medical condition in which there is significant reduction in the number of almost all blood cells (red blood cells, white blood cells, platelets, monocytes, lymphocytes, etc.). If only two parameters from the complete blood count are low, the term bicytopenia can be used.

  3. Cytopenia - Wikipedia

    en.wikipedia.org/wiki/Cytopenia

    Pancytopenia – when all three types of blood cells; red blood cells, white blood cells, and platelets, are all deficient. This is a life-threatening disorder that is a characteristic of aplastic anemia. [3]

  4. Ataxia-pancytopenia syndrome - Wikipedia

    en.wikipedia.org/wiki/Ataxia-pancytopenia_syndrome

    Ataxia-pancytopenia syndrome, also known as myelocerebellar dysfunction, was first described by Frederick Pei Li in 1978. The father and all five of his children developed ataxia and hematologic cytopenias of varying severity during their first to third decades of life.

  5. Reticulocytopenia - Wikipedia

    en.wikipedia.org/wiki/Reticulocytopenia

    If pancytopenia is present, bone marrow failure [4] must be considered and evaluation for bone marrow failure syndromes or aplastic anemia must be pursued. Treatment is dependent on the etiology and may include replacement of blood products as patients can develop severe anemia.

  6. Congenital amegakaryocytic thrombocytopenia - Wikipedia

    en.wikipedia.org/wiki/Congenital_amegakaryocytic...

    Type I-CAMT is more severe and is characterized by low platelet counts and an early progression of bone marrow aplasia associated with pancytopenia. [ 1 ] The second type of Congenital amegakaryocytic thrombocytopenia is milder and presents with a transient increase of platelet counts during the first year of life.

  7. Primary myelofibrosis - Wikipedia

    en.wikipedia.org/wiki/Primary_myelofibrosis

    The decrease in hematopoietic tissue impairs the patient's ability to generate new blood cells, resulting in progressive pancytopenia, a shortage of all blood cell types. However, the proliferation of fibroblasts and deposition of collagen is a secondary phenomenon, and the fibroblasts themselves are not part of the abnormal cell clone.

  8. Hemophagocytic lymphohistiocytosis - Wikipedia

    en.wikipedia.org/wiki/Hemophagocytic_lymphohist...

    This is a rare autosomal recessive disorder characterized by partial albinism, hepatosplenomegaly, pancytopenia, hepatitis, immunologic abnormalities, and lymphohistiocytosis. Most cases have been diagnosed between 4 months and 7 years of age, with a mean age of about 17 months. [citation needed]

  9. Subleukemic leukemia - Wikipedia

    en.wikipedia.org/wiki/Subleukemic_leukemia

    Pancytopenia is a disease where an individual has lower than average numbers of red and white blood cells, as well as platelets. This condition can lead to leukemia or other blood diseases. The prevalence of subleukemic leukemia in individuals with pancytopenia is currently known to be between 3-12%.