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409 Possible Causes for Hepatomegaly, Polycythemia Vera

  • Myeloproliferative Disease

    […] mice from two independent transgenic lines and from backcrosses into either the FVB or the C57BL/6 strains succumbed to a similar disease characterized by splenomegaly, hepatomegaly[ncbi.nlm.nih.gov] Polycythemia vera, essential thrombocythemia, and idiopathic myelofibrosis are clonal myeloproliferative disorders arising from a multipotent progenitor.[ncbi.nlm.nih.gov] Splenomegaly, hepatomegaly as well as fatigue, malaise or weight loss may appear in advanced stages.[orpha.net]

  • Primary Myelofibrosis

    The patient, a 62-year-old female, having had primary myelofibrosis for 13 years and a splenectomy 4 years before, was admitted because of high fever, hepatomegaly, thrombocythemia[ncbi.nlm.nih.gov] Megakaryocytes are the "hallmark" of Philadelphia chromosome-negative myeloproliferative neoplasms, such as essential thrombocythemia, polycythemia vera, and primary myelofibrosis[ncbi.nlm.nih.gov] […] manifestations depend on the type of blood cell affected and may include anemia, pallor, splenomegaly, hypermetabolic state, petechiae, ecchymosis, bleeding, lymphadenopathy, hepatomegaly[orpha.net]

  • Polycythemia Vera

    Symptoms of Budd-Chiari syndrome include pain in the upper right part of the abdomen, an abnormally enlarged liver (hepatomegaly), yellowing of the skin and the whites of[rarediseases.org] How is polycythemia vera treated?[symptoma.com] […] women) Plethora Pruritus after bathing Splenomegaly Weight loss Weakness Sweating Less Common Bruising/epistaxis Budd-Chiari syndrome Erythromelalgia Gout Hemorrhagic events Hepatomegaly[aafp.org]

  • Essential Thrombocythemia

    PHYSICAL EXAMINATION • Unremarkable • 40-50% present with splenomegaly • 20% present with hepatomegaly 12.[slideshare.net] This review provides our current management strategy of patients with polycythemia vera and ET. Copyright 2016 Elsevier Inc. All rights reserved.[ncbi.nlm.nih.gov] In some cases the liver may also be enlarged (hepatomegaly). Other symptoms include weight loss and generalised itching.[leukaemia.org.au]

  • Chronic Phase of Chronic Myeloid Leukemia

    Hepatomegaly. Enlarged lymph nodes are also a possibility. Anaemia can produce a hyperdynamic circulation. Easy bruising. Fever. Gout due to rapid cell turnover.[patient.info] "Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations[en.wikipedia.org]

  • Budd-Chiari Syndrome

    Budd-Chiari Syndrome (BCS) is a hepatic venous outflow tract obstruction and involves abdominal pain, hepatomegaly and high-gradient ascites.[ncbi.nlm.nih.gov] Polycythemia vera is a Philadelphia chromosome-negative myeloproliferative disorder with incidence of 1% under the age of 25.[ncbi.nlm.nih.gov] A 10-month-old boy presented with ascites, right pleural effusion, and hepatomegaly after consumption of herbal drinks for 3 months.[ncbi.nlm.nih.gov]

  • Post-Polycythemia Vera Myelofibrosis

    Presence of diabetes or another neoplasia was associated with higher ROS levels (p 0.05), splenomegaly, hepatomegaly, and peripheral blasts with lower HoloTC levels (p 0.005[ncbi.nlm.nih.gov] Post-polycythemia vera myelofibrosis is a condition in which polycythemia vera, a disorder of excessive red cell production, triggers malignant transformation of hematopoietic[symptoma.com] If hepatomegaly occurs, patients might also have variceal bleeding related to portal hypertension or ascites. B.[clinicaladvisor.com]

  • Familial Myelofibrosis

    In case of hepatomegaly, the liver extends to more than 3 cm below the right costal margin of the newborn.[symptoma.com] 雑誌名 Blood Advances 巻 : 1 ページ : 1001-1015 DOI 関連する報告書 査読あり / オープンアクセスとしている / 国際共著/国際学会である [雑誌論文] The 2016 WHO diagnostic criteria for polycythemia vera renders an accurate[kaken.nii.ac.jp] For instance, polycythemia vera may be inherited in an autosomal dominant manner and predisposes to myelofibrosis.[symptoma.com]

  • Ayerza Syndrome

    In the cardiovascular examination there was jugular venous distension, hepatomegaly, hepatojugular reflux, ascites and oedema of lower limbs.[err.ersjournals.com] vera but resulting from primary pulmonary arteriosclerosis or primary pulmonary hypertension and characterized by plexiform lesions of arterioles.[medical-dictionary.thefreedictionary.com] Term: Pronunciation: ah-yār′shah Definition: sclerosis of the pulmonary arteries in chronic cor pulmonale; associated with severe cyanosis, it is a condition resembling polycythemia[rxmed.info]

  • Acute Myelocytic Leukemia

    Multivariate analysis showed that grades 1 or 2 GVHD (P .008) and no hepatomegaly at diagnosis (P .014) were associated with improved relapse-free survival (RFS).[ncbi.nlm.nih.gov] Abstract A t(11;20)(p15;q11) is a rare but recurrent chromosomal aberration, reported in one case of polycythemia vera and a few cases of de novo acute myelocytic leukemia[ncbi.nlm.nih.gov] vera and myeloproliferative disorders (for example, chronic myelogenous leukemia ) Some birth defects and disorders, such as Down syndrome Being male Although there is no[webmd.com]

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