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210 Possible Causes for Hypercellular Bone Marrow, Thromboembolism

  • Paroxysmal Nocturnal Hemoglobinuria

    KEYWORDS: Paroxysmal nocturnal hemoglobinuria; Venous thromboembolism[] 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[] Table 2 Sites of pretreatment thromboembolism events Main outcome measure.[]

  • Myeloproliferative Disease

    BACKGROUND: Splenectomy is a risk factor for both portal-vein and chronic thromboembolic pulmonary hypertension.[] The chronic myeloproliferative diseases are characterized by relatively effective hematopoiesis, which results in a hypercellular bone marrow and elevation of one or more[] Bone marrow histology shows hypercellularity in most of these disorders. In the case of myelofibrosis, bone marrow fibrosis is demonstrated on the reticulin stain.[]

  • Polycythemia Vera

    BACKGROUND: Patients with polycythemia vera (PV) are at increased risk of thromboembolic events (TEs), which are key contributors to reduced overall survival compared with[] bone marrow 5.[] We present a 62-year-old male in a hypercoagulable state due to primary polycythemia vera (PV) developed TAMT and catastrophic thromboembolisms despite aggressive medical[]

  • Secondary Polycythemia

    KEYWORDS: obesity; phlebotomy; polycythemia; venous thromboembolism[] The renal biopsy revealed membranous nephropathy, and the bone marrow biopsy disclosed hypercellular marrow with mild panhyperplasia.[] Bone marrow is hypercellular with prominent megakaryocytes. Serum erythropoietin level is usually low. Blood viscosity is increased.[]

  • Chronic Myeloid Leukemia

    […] efficacy in patients with refractory CML, but is associated with an increased risk of arterial hypertension, sometimes severe, and serious arterial occlusive and venous thromboembolic[] marrow biopsy: Moderately hypercellular bone marrow biopsy with numerous megakaryocytes Increased reticulin fibers (reticulin stain) Marked hypercellularity Myeloblastic[] […] tyrosine kinase inhibitor treatment, the main goal was to reduce the leukocyte count to postpone delivery beyond the number of weeks considered severely premature and avoid thromboembolic[]

  • Ayerza Syndrome

    Computerized tomography: Useful in chronic thromboembolic pulmonary arterial hypertension. Magnetic resonance imaging (MRI).[] "Chronic thromboembolic pulmonary hypertension". Circulation. 113 (16): 2011–20. doi : 10.1161/CIRCULATIONAHA.105.602565. PMC 4357025. PMID 16636189.[] Primary and thromboembolic pulmonary hypertension, quantitative pathological study, J. Path., v. 110, No. 4, p. 273, 1973, bibliogr.; Barrett A. M. a. Cole L.[]

  • Chronic Phase of Chronic Myeloid Leukemia

    marrow biopsy: Moderately hypercellular bone marrow biopsy with numerous megakaryocytes Increased reticulin fibers (reticulin stain) Marked hypercellularity Myeloblastic[] A bone marrow biopsy and aspiration demonstrated a hypercellular marrow with no other significant morphologic abnormalities.[] marrow Early myeloid cells (eg, myeloblasts, myelocytes, metamyelocytes, nucleated red blood cells) Bone marrow findings Ph chromosome (a reciprocal translocation of chromosomal[]

  • Sickle Cell Disease

    Abstract Patients with sickle cell disease (SCD) experience initial and recurrent venous thromboembolism (VTE) more commonly and at a younger age than the general population[] We herein report an unusual SCD case, complicated by chronic thromboembolic disorder, who developed severe TR and an accelerated progression of PH.[] Homozygous individuals are likely at increased risk for thromboembolic complications.[]

  • Primary Myelofibrosis

    During initial stages of the disease, thrombocytosis accounts for symptoms like thrombosis and thromboembolism.[] A biopsy of the lytic lesion was done, revealing hypercellular bone marrow with hyperplastic granulopoiesis associated with megakaryocytic proliferation and atypia, accompanied[] (A) Other cancers, including (B) skin carcinoma, (C) development of myelofibrosis and (D) thromboembolic events (lethal or not) according to the treatment received.[]

  • Autoimmune Hemolytic Anemia

    OBJECTIVE: To investigate the risk of venous thromboembolism (VTE) among patients with autoimmune hemolytic anemia (AIHA).[] Subsequently, the patient underwent a bone marrow biopsy that showed a hypercellular marrow with erythroid hyperplasia, but no evidence of dysplasia or lymphoma.[] BACKGROUND: The risk of venous thromboembolism (VTE) during warm autoimmune hemolytic anemia (wAIHA) is apparent in several published series.[]

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