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358 Possible Causes for Hematocrit Decreased, Thrombocytopenic Purpura

  • HELLP Syndrome

    The laboratory investigations before death revealed evidence of hemolysis, which is decreased hematocrit, elevated lactate dehydrogenase (865 U/L), and low platelet count[] CONCLUSION: Thrombotic thrombocytopenic purpura can mimic HELLP syndrome late in gestation.[] […] normal: decreased serum haptoglobin levels may be present indicating HELLP) [2] Liver Enzymes: As high as 4,000 U per L [2] Platelets: As low as 6,000 per mm 3 ( anything[]

  • Anemia

    Hemolytic anemia This type of anemia includes sickle cell anemia, thrombotic thrombocytopenic purpura (TTP), hemolytic uremic syndrome, aortic valve prosthesis, disseminated[] Throughout fetal life, erythrocytes decrease in size and increase in number: hematocrit increases from 30% to 40% during the second trimester to 50% to 63% at term.[] Helmet cells and schistocytes are found in microangiopathic hemolysis (eg, thrombotic thrombocytopenic purpura [TTP], immune thrombocytopenic purpura [ITP], hemolytic-uremic[]

  • Chronic Immune Thrombocytopenic Purpura

    Hematuria is an uncommon manifestation of chronic immune thrombocytopenic purpura.[] Immune thrombocytopenic purpura is a disorder affecting all age groups.[] purpura.[]

  • Immune Thrombocytopenic Purpura

    Immune thrombocytopenic purpura (ITP), also called primary immune thrombocytopenia or idiopathic thrombocytopenic purpura, is an autoimmune disease affecting thrombocytes.[] Incidences of immune thrombocytopenic purpura occur in 1 in every 1000-10,000 pregnancies accounting for 3% of all thrombocytopenic pregnancies.[] Chronic idiopathic thrombocytopenic purpura Idiopathic thrombocytopenia purpura (itp) Idiopathic thrombocytopenic purpura Idiopathic thrombocytopenic purpura, (itp), chronic[]

  • Autoimmune Hemolytic Anemia

    The differential white blood count shows a decrease in most types of cells but not lymphocytes .[] An elevated CRP has been recently recognized as an important prognostic marker in patients with immune thrombocytopenic purpura and this case suggests a need to evaluate its[] DIC (disseminated intravascular coagulation)and TTP (thrombotic thrombocytopenic purpura) - DIC (disseminated intravascular coagulation)and TTP (thrombotic thrombocytopenic[]

  • Cerebral Thrombotic Thrombocytopenic Purpura

    KEYWORDS: Cerebral microbleeds; MRI; ischemic stroke; thrombotic thrombocytopenic purpura[] He also had melena with rapid decline in hematocrit and was treated with single dose of IVIg 75 g.[] Key words: Thrombotic thrombocytopenic purpura, generalized tonic clonic seizer, cerebral venus sinus thrombosis[]

  • Atypical Hemolytic Uremic Syndrome

    Since the last review in 2007 of thrombotic thrombocytopenic purpura (TTP) and microangiopathic hemolytic anemia in the Clinics, further understanding of the nature of TTP[] hematocrit and hemoglobin and thrombocytopenia ; schistocytes on peripheral blood smears, elevated LDH, low haptoglobin, elevated indirect bilirrubin, elevated reticulocytes[] Thrombotic thrombocytopenic purpura (TTP) and atypical hemolytic uremic syndrome (aHUS) are thrombotic microangiopathies (TMAs) that can present in pregnancy.[]

  • Disseminated Intravascular Coagulation

    We report on 3 male neonates with hereditary ADAMTS13 deficiency (Upshaw Schulman syndrome, USS), the inherited form of thrombotic thrombocytopenic purpura (TTP). 2 presented[] In contrast, disseminated intravascular microthrombosis (DIT) occurs in thrombotic thrombocytopenic purpura (TTP) and TTP-like syndrome due to ADAMTS13 deficiency or insufficiency[] Our investigations subsequently excluded thrombotic thrombocytopenic purpura and Shiga toxin-producing Escherichia coli-induced HUS.[]

  • Microangiopathic Hemolytic Anemia

    The similarity of the mother's illness to thrombotic thrombocytopenic purpura and of the daughter's to adult hemolytic uremic syndrome suggests that these diseases are variants[] Our understanding of the pathogenesis of idiopathic thrombotic thrombocytopenic purpura (TTP) has increased, but remains incomplete, particularly with respect to cases of[] The similarity of the mother’s illness to thrombotic thrombocytopenic purpura and of the daughter’s to adult hemolytic uremic syndrome suggests that these diseases are variants[]

  • Hypersplenism

    Splenectomy is one of the primary choices of treatment in immune thrombocytopenic purpura. However, the disease may relapse despite splenectomy.[] METHODS: From Aug 2014 to Dec 2014, four children with hypersplenism and three children with idiopathic thrombocytopenic purpura were treated in our hospital.[] Primary causes are idiopathic thrombocytopenic purpura, congenital hemolytic anaemia and primary splenic neutropenia or pancytopenia.[]

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