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156 Possible Causes for Hypercellular Bone Marrow, Primary Myelofibrosis

  • Leukemia

    Bone marrow aspirate showed hypercellularity with increased myelopoiesis and markedly suppressed megakaryopoiesis giving an impression of acute myeloid leukemia and was confirmed[] […] description ICD-O3 code Myeloproliferative neoplasms Chronic myelogenous leukaemia, BCR-ABL1 positive 9975/3 Chronic neutrophilic leukaemia 9963/3 Polycythaemia vera 9950/3 Primary[] Another important feature of bone marrow samples is its cellularity. Normal bone marrow contains hematopoietic (blood-forming) cells and fat cells.[]

  • Polycythemia Vera

    bone marrow 5.[] Megakaryocytic morphology also differed between primary myelofibrosis JAK2 V617F and essential thrombocythemia JAK2 V617F.[] Based on the presence of severe hypercellularity of the bone marrow and positivity for the JAK2V617F mutation, we finally diagnosed the patient with PV.[]

  • Chronic Myeloid Leukemia

    marrow biopsy: Moderately hypercellular bone marrow biopsy with numerous megakaryocytes Increased reticulin fibers (reticulin stain) Marked hypercellularity Myeloblastic[] myelofibrosis (PMF).[] Table 5 2001 WHO criteria for prefibrotic stage primary myelofibrosis Table 6 2001 WHO criteria for fibrotic stage primary myelofibrosis Table 7 Proposed revised WHO criteria[]

  • Chronic Phase of Chronic Myeloid Leukemia

    "Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations[] marrow biopsy: Moderately hypercellular bone marrow biopsy with numerous megakaryocytes Increased reticulin fibers (reticulin stain) Marked hypercellularity Myeloblastic[] myelofibrosis (PMF), and polycythemia vera (PV).[]

  • Myeloproliferative Disease

    The chronic myeloproliferative diseases are characterized by relatively effective hematopoiesis, which results in a hypercellular bone marrow and elevation of one or more[] Most of the remaining minority of patients with primary myelofibrosis and essential thrombocythemia have a mutation in the CALR or MPL genes.[] Bone marrow histology shows hypercellularity in most of these disorders. In the case of myelofibrosis, bone marrow fibrosis is demonstrated on the reticulin stain.[]

  • Paroxysmal Nocturnal Hemoglobinuria

    These patients tend to have a normocellular to hypercellular bone marrow with erythroid hyperplasia, an elevated reticulocyte count, a large population of PNH cells (usually[] Thrombosis is the leading cause of death, but others may die of complications of bone marrow failure, renal failure, myelodysplastic syndrome, and leukemia.[]

  • Chronic Neutrophilic Leukemia

    bone marrow with predominant neutrophilic granulopoiesis (M:E is 20:1 or more), the number of myeloblasts and promyelocytes is not increased, myelocytes and mature neutrophils[] In this study, we clarify the difference in serum G-CSF levels between patients with primary myelofibrosis (PMF, myelofibrosis with myeloid metaplasia; MMM) and those with[] Keywords: Myeloproliferative neoplasm, polycythemia vera, essential thrombocythemia, primary myelofibrosis, chronic idiopathic myelofibrosis, myeloid metaplasia, chronic neutrophilic[]

  • Secondary Polycythemia

    The renal biopsy revealed membranous nephropathy, and the bone marrow biopsy disclosed hypercellular marrow with mild panhyperplasia.[] The diagnosis and management of polycythemia vera, essential thrombocythemia, and primary myelofibrosis in the JAK2 V617F era.[] Bone marrow is hypercellular with prominent megakaryocytes. Serum erythropoietin level is usually low. Blood viscosity is increased.[]

  • Myelodysplasia

    bone marrow Hello all, On my BMB report, for the bone marrow, it states "hypercellular ... 3 days, 8 hours ago CENTERS OF EXCELLENCE Would you like your treatment center[] primary MDS (often RAEB2 ) with fibrosis and therapy related myeloid neoplasms with fibrosis Primary Myelofibrosis, Fibrotic Phase MDS with Fibrosis Post-Polycythemia Vera[] The primary morphologic finding is that of dysplasia in a cytopenic patient and, typically, a hypercellular bone marrow.[]

  • Acute Panmyelosis with Myelofibrosis

    (AMKL-MF), primary myelofibrosis (PMF) and myelodysplastic syndrome with myelofibrosis (MDS-MF) in order to provide the keys to the differential diagnosis of bone marrow[] marrow aspirate was unsuccessful but bone marrow biopsy ( Figure 2 ) revealed hypercellular bone marrow with panmyeloid proliferation.[] ) myelophthisic anemia ( D61.82 ) myelophthisis ( D61.82 ) primary myelofibrosis ( D47.1 ) Use Additional code, if applicable, for associated therapy-related myelodysplastic[]

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