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  2. Schistocyte - Wikipedia

    en.wikipedia.org/wiki/Schistocyte

    Peripheral blood smear in patient with thrombotic thrombocytopenic purpura. Typical schistocytes are annotated. A schistocyte or schizocyte (from Greek schistos for "divided" and kytos for "hollow" or "cell") is a fragmented part of a red blood cell. Schistocytes are typically irregularly shaped, jagged, and have two pointed ends. [1]

  3. Spherocytosis - Wikipedia

    en.wikipedia.org/wiki/Spherocytosis

    Spherocytosis is the presence of spherocytes in the blood, i.e. erythrocytes (red blood cells) that are sphere-shaped rather than bi-concave disk shaped as normal. Spherocytes are found in all hemolytic anemias to some degree. Hereditary spherocytosis and autoimmune hemolytic anemia are characterized by having only spherocytes. [1]

  4. Microangiopathic hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Microangiopathic_hemolytic...

    Schistocytes or helmet cells . Diagnosis. Microangiopathic hemolytic anemia results in isolated increase in serum bilirubin levels. Unconjugated hyperbilirubinemia ...

  5. Acanthocyte - Wikipedia

    en.wikipedia.org/wiki/Acanthocyte

    Acanthocytes, from peripheral blood, under light microscopy. Note the irregularly shaped, non-circular cells in the image. Acanthocyte (from the Greek word ἄκανθα acantha, meaning 'thorn'), in biology and medicine, refers to an abnormal form of red blood cell that has a spiked cell membrane, due to thorny projections.

  6. Drug-induced autoimmune hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Drug-induced_autoimmune...

    In some cases, a peripheral blood smear may show schistocytes, anisocytosis, polychromasia, or poikilocytosis. [7] Direct antiglobulin testing is the only way to confirm DIIHA. Direct antiglobulin testing can determine if complement C3 antibody and/or immunoglobulin G is bound to the red blood cell membrane. [4]

  7. Autoimmune hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_hemolytic_anemia

    Spherocytes are found in immunologically mediated hemolytic anemias. [11] Signs of hemolysis that are present in AIHA include low hemoglobin (blood count), alterations in levels of cell markers of hemolysis; including elevated lactate dehydrogenase (LDH) , decreased haptoglobin and elevated unconjugated bilirubin . [ 4 ]

  8. Hereditary spherocytosis - Wikipedia

    en.wikipedia.org/wiki/Hereditary_spherocytosis

    Hereditary spherocytosis is the heritable hemolytic disorder, affecting 1 in 2,000 people of Northern European ancestry. [5] According to Harrison's Principles of Internal Medicine, the frequency is at least 1 in 5,000 within the United States of America. [6]

  9. Poikilocytosis - Wikipedia

    en.wikipedia.org/wiki/Poikilocytosis

    Poikilocytosis is variation in the shapes of red blood cells.Poikilocytes may be oval, teardrop-shaped, sickle-shaped or irregularly contracted. Normal red blood cells are round, flattened disks that are thinner in the middle