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  2. Primary myelofibrosis - Wikipedia

    en.wikipedia.org/wiki/Primary_myelofibrosis

    Diagnosis is made on the basis of bone marrow biopsy. Fibrosis grade 2 or 3 defines overt PMF whereas grade 0 or 1 defines prefibrotic primary myelofibrosis. [citation needed] A physical exam of the abdomen may reveal enlargement of the spleen, the liver, or both. [3] Bone marrow biopsy shows fibrosis of the bone marrow.

  3. Prefibrotic primary myelofibrosis - Wikipedia

    en.wikipedia.org/wiki/Prefibrotic_primary_myelo...

    The bone marrow histology should demonstrate the following: [2] A proliferation and atypia of the bone marrow cells that produce platelets (megakaryocytes) Reticulin fibrosis which doesn't exceed grade 1. Grade 2 or 3 is a diagnostic criteria for primary myelofibrosis. Age-adjusted cellularity

  4. Myelodysplastic syndrome - Wikipedia

    en.wikipedia.org/wiki/Myelodysplastic_syndrome

    The prognosis depends on the type of cells affected, the number of blasts in the bone marrow or blood, and the changes present in the chromosomes of the affected cells. [3] The average survival time following diagnosis is 2.5 years. [ 4 ]

  5. Fibrous dysplasia of bone - Wikipedia

    en.wikipedia.org/wiki/Fibrous_dysplasia_of_bone

    Bone pain is a common complication of fibrous dysplasia. It may present at any age, but most commonly develops during adolescence and progresses into adulthood. [7] Bone marrow stromal cells in fibrous dysplasia produce excess amounts of the phosphate-regulating hormone fibroblast growth factor-23 (FGF23), leading to loss of phosphate in the ...

  6. Acute panmyelosis with myelofibrosis - Wikipedia

    en.wikipedia.org/wiki/Acute_panmyelosis_with_mye...

    Bone biopsy shows abnormal megakaryocytes, macrocytic erythropoiesis, and defects in neutrophil production and fibrosis of the marrow (myelofibrosis).. Clinically, patients present with reduction in the count of all blood cells (pancytopenia), very few blasts in the peripheral blood, and no or little spleen enlargement (splenomegaly).

  7. Myelophthisic anemia - Wikipedia

    en.wikipedia.org/wiki/Myelophthisic_anemia

    Myelophthisic anemia (or myelophthisis) is a severe type of anemia found in some people with diseases that affect the bone marrow. Myelophthisis refers to the displacement of hemopoietic bone-marrow tissue [1] by fibrosis, tumors, or granulomas. The word comes from the roots myelo-, which refers to bone marrow, and phthisis, shrinkage or atrophy.

  8. Myeloproliferative neoplasm - Wikipedia

    en.wikipedia.org/wiki/Myeloproliferative_neoplasm

    Myeloproliferative neoplasms (MPNs) are a group of rare blood cancers in which excess red blood cells, white blood cells or platelets are produced in the bone marrow. Myelo refers to the bone marrow, proliferative describes the rapid growth of blood cells and neoplasm describes that growth as abnormal and uncontrolled.

  9. Hypereosinophilic syndrome - Wikipedia

    en.wikipedia.org/wiki/Hypereosinophilic_syndrome

    While some HES patients have eosinophilia in conjunction with known myeloid malignancies, others do not have a known malignancy but do have laboratory or bone marrow abnormalities, such as thrombocytopenia, anemia, hepatosplenomegaly, and eosinophil-related tissue damage and fibrosis, that are frequently associated with myeloproliferative ...