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

  • Polycythemia Vera

    Symptoms may include: Abnormal and heavy bleeding due to a cut or a nosebleed Intense and frequent bone pain and/or muscle pain Headaches, lightheadedness or gastrointestinal[] bone marrow 5.[] Keywords: Erythromelalgia - essential thrombocythemia - polycythemia vera - myeloproliferative disorders - thrombosis[]

  • Myeloproliferative Disease

    Symptoms Signs  Fatigue  Malaise  Early satiety  Weight loss  Fever  Abdominal painBone pain  Pruritis  Splenomegaly  Abnormal blood counts  Abnormal peripheral[] Image shows: PV bone marrow (hypercellular) Picture of normal bone marrow for comparison Myeloproliferative Disorders: -Polycythemia Vera (PV) * Peripheral blood findings[] Essential thrombocythemia (ET) was suspected by a sustained increase in platelet count ( 400 x 10(9)/l) and slight splenomegaly on echogram.[]

  • 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

    pain,... )[] marrow biopsy: Moderately hypercellular bone marrow biopsy with numerous megakaryocytes Increased reticulin fibers (reticulin stain) Marked hypercellularity Myeloblastic[] Table 3 2001 World Health Organization criteria for essential thrombocythemia Table 4 Proposed revised WHO criteria for essential thrombocythemia (ET) In addition, we propose[]

  • Primary Myelofibrosis

    Involved field radiotherapy is most useful for post-splenectomy hepatomegaly, non-hepatosplenic EMH, PMF-associated pulmonary hypertension, and extremity bone pain.[] There is a stepwise evolution from an initial pre/fibrotic early stage, characterized by hypercellular bone marrow with absent or minimal reticulin fibrosis , to an overt[] Megakaryocytic morphology also differed between primary myelofibrosis JAK2 V617F and essential thrombocythemia JAK2 V617F.[]

  • Acute Leukemia

    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[] thrombocythemia and myelodysplastic syndromes (MDS) Previous chemotherapy or radiation treatments for other cancers Symptoms The signs and symptoms of AML are mainly the[]

  • 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.[]

  • Myelofibrosis

    […] vera myelofibrosis, or post-essential thrombocythemia ...[] METHODS: We reported on a case of a patient with MF who presented with weight loss and cachexia associated with severe anemia, fatigue, fever, and bone pain.[] Essential for diagnosis: Tear drop poikilocytosis on peripheral smear Leukoerythroblastic blood picture ,giant abnormal platelets Hypercellular bone marrow with reticulin[]

  • Chronic Neutrophilic Leukemia

    Abstract 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.[] marrow Hypercellular bone marrow biopsy with increased neutrophils showing no overt dysplasia, normal megakaryocytes Hepatosplenomegaly No reactive cause for neutrophilia[] The main MPN entities discussed in this chapter are polycythemia vera, essential thrombocythemia, and primary myelofibrosis.[]

  • Systemic Mastocytosis

    […] patients reported improvement in bone pain after bisphosphonate treatment.[] Bone marrow biopsy.[] Bone marrow trephine biopsy examination (histology and immunohistochemistry for CD117 and CD25) revealed a SM associated with CMN, essential thrombocythemia (ET) type.[]

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