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96 Possible Causes for Bone Pain, Essential Thrombocythemia, Hypercellular Bone Marrow

  • Myeloproliferative Disease

    Splanchnic vein thrombosis (SVT) is a severe complication of essential thrombocythemia (ET).[] Symptoms Signs  Fatigue  Malaise  Early satiety  Weight loss  Fever  Abdominal painBone pain  Pruritis  Splenomegaly  Abnormal blood counts  Abnormal peripheral[] 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

    Treatments for Symptoms Aspirin can relieve bone pain and burning feelings in your hands or feet that you may have as a result of PV.[] bone marrow 5.[] Keywords: Erythromelalgia - essential thrombocythemia - polycythemia vera - myeloproliferative disorders - thrombosis[]

  • Chronic Phase of Chronic Myeloid Leukemia

    […] marrow to other tissues and organs CML cells with new chromosome abnormalities Symptoms such as Fever Fatigue Shortness of breath Abdominal pain Bone pain Enlarged spleen[] marrow biopsy: Moderately hypercellular bone marrow biopsy with numerous megakaryocytes Increased reticulin fibers (reticulin stain) Marked hypercellularity Myeloblastic[] thrombocythemia have a platelet count greater than 450,000 3 - Myelofibrosis - teardrop poikilocytes and other severe red cell shape, size, and chromicity changes JAK2 (PV[]

  • Chronic Myeloid Leukemia

    While the peripheral blood and bone marrow findings initially suggested essential thrombocythemia, BCR-ABL1 translocation was detected and chronic myeloid leukemia, chronic[] pain,... )[] marrow biopsy: Moderately hypercellular bone marrow biopsy with numerous megakaryocytes Increased reticulin fibers (reticulin stain) Marked hypercellularity Myeloblastic[]

  • Primary Myelofibrosis

    Involved field radiotherapy is most useful for post-splenectomy hepatomegaly, non-hepatosplenic EMH, PMF-associated pulmonary hypertension, and extremity bone pain.[] A biopsy of the lytic lesion was done, revealing hypercellular bone marrow with hyperplastic granulopoiesis associated with megakaryocytic proliferation and atypia, accompanied[] Megakaryocytic morphology also differed between primary myelofibrosis JAK2 V617F and essential thrombocythemia JAK2 V617F.[]

  • Leukemia

    Table 3 Criteria for polycythemia vera (PV) Table 4 Criteria for essential thrombocythemia (ET) Table 5 Criteria for primary myelofibrosis (PMF) Recently, some authorities[] So, it's more generalized bone pain.[] Bone marrow aspirate showed hypercellularity with increased myelopoiesis and markedly suppressed megakaryopoiesis giving an impression of acute myeloid leukemia and was confirmed[]

  • Acute Leukemia

    thrombocythemia and myelodysplastic syndromes (MDS) Previous chemotherapy or radiation treatments for other cancers Symptoms The signs and symptoms of AML are mainly the[] Herein we present a standard risk pediatric acute lymphobiastic leukemia patient who developed myalgia, bone pain, bone marrow aplasia and sinusoidal obstruction syndrome[] ALL : Hypercellular bone marrow Numerous tightly packed lymphoblasts with undetectable cytoplasm, round, irregular, cleaved nuclei, dispersed chromatin, small nucleoli B[]

  • Myelofibrosis

    Conclusions Bone and joint pain is the common symptom of cancer.[] Essential for diagnosis: Tear drop poikilocytosis on peripheral smear Leukoerythroblastic blood picture ,giant abnormal platelets Hypercellular bone marrow with reticulin[] […] vera myelofibrosis, or post-essential thrombocythemia ...[]

  • Secondary Polycythemia

    For example, antihistamines can alleviate itching, and aspirin can soothe burning sensations and bone pain.[] 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.[]

  • Chronic Neutrophilic Leukemia

    A 60-year-old woman who presented with weakness, night sweats, bone pain, easy bruising and weight loss was found to have ecchymoses and hepatosplenomegaly.[] 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[] The main MPN entities discussed in this chapter are polycythemia vera, essential thrombocythemia, and primary myelofibrosis.[]

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