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Summary of Abnormal Red Blood Cell Morphologies and Disease States



  • Before we start with the abnormal morphologies, let’s talk about normal morphology of Red Blood Cells.
  • Normal mature RBC are biconcave, round discs that are about 6 – 8 in diameter, which is only slightly smaller than the normal small mature lymphocytes ( about 6 – 10 in diameter).
  • The term used to indicate red blood cells of normal size and shape is normocytic. The term used to indicate a normal color or central pallor (i.e., normal hemoglobin content) is normochromic
  • Normocytic and Normochromic RBC
  • Hypochromic: Erythrocytes that demonstrate a central pale area that becomes larger and paler as the hemoglobin content diminishes

  1. Iron Deficiency
  2. Sideroblastic Anaemia
  3. Thalassaemia
  • Hypochromic RBC

    Anisochromic: indicates the presence of both normochromic and Hypochromic

  • Anisochromic (Normochromic plus Hypochromic)

  • Polychromasia: Changeable terms used to indicate the increased presence of non-nucleated immature erythrocytes (Polychromatophilic erythrocytes) that contain residual RNA which gives a blue-gray tint to the red cells. These cells, which remain after ejection of the nucleus from the orthochromatic erythroblast are slightly larger than mature erythrocytes. After exposure to a supravital stain, the cytoplasm organelles of these cells clump into an easily recognized blue-staining reticulum and the cells is called a reticulocytes.




    • Polychromasia
      Anisocytosis:  is a “generic” term used to indicate variation in shape of erythrocytes (e.g. oval, pear-shaped, teardrop-shaped, saddle-shaped, helmet-shaped, sickle-shaped, and irregularly shaped).
    Anisocytosis

    Microcytosis: abnormally small erythrocytes (i.e., less than 6 in diameter). compare with the size for small lymphocyte.
    • Found with Hypochromic
    Microcytosis

    Macrocytosis: abnormally large erythrocytes (i.e., less than 8 in diameter).
    • Megaloblastic Anaemia
    • High reticulocytes count
    • Liver disease
    • Myelodysplastic syndrome
    Macrocytosis
    Target Cells (Codocytes): erythrocytes that are thinner than normal which show a peripheral rim of hemoglobin with a dark central hemoglobin-containing area. A pale unstained ring containing less hemoglobin separates the central and peripheral zones and gives the cell a target appearance.
    • Liver Disease
    • Hemoglobinopathies
    • Thalassaemia
    • Sideroblastic anemia
      Target Cells

Spherocytes: are nearly spherical erythrocytes which are nearly spherical erythrocytes which usually have a diameter smaller than normal. They lack the central pale area due to their spherical shape.
  • Hemolytic anemia
  • Post transfusion
  • Hereditary sphercocytosis
  • Spherocytes


Tear-Drop Cells:
  • Severe Anaemia
  • Myloproliferative disorders
Teardrop cells (dacrocytes)

Elliptocytes and Ovalocytes: are interchangeable terms used to indicate ovalshaped erythrocytes.
  • Hereditary elliptocytosis
  • Iron-deficiency anaemia
  • Thalassaemia
Elliptocytes

Stomatocytes:
  • Acute alcoholism
  • Malignancies
  • Stomatocytes

Helmet Cells:
  • G6PD deficiency
  • Pulmonary emboli


Helmet Cells (Keratocytes)


Schistocytes: are fragmented red cell segments that are the result of some hemolytic process. These segments can be a variety of shapes but helmet cells and triangularly-shaped cells are particularly characteristic.
  • Disseminated intra-vascular coagulopathy (DIC)
  • Thrombotic Thrombocytopenia purpura (TTP)
  • Hemolytic uremic syndrome (HUS)
Schistocytes


Sickle cells (drepanocyes): are interchangeable terms used to indicate sickle-like forms of erythrocytes (crescent-shaped, irregular spines, filaments, holly-leaf appearance) noted when RBC containing HbS are subjected to reduction in oxygen tension or pH.
  • Sickle cell anaemia
  • Sickle thalassaemia

Sickle Cells


Acanthocytes (Spur Cell):
  • Congenital abetalipoproteinemia
  • Vitamin E deficiency
  • Alcohol intoxication
  • Post-splenectomy
Acanthocytes



Burr Cells:
  • Liver disease
  • Renal disease
  • Severe burns
  • Bleeding gastric ulcers
  • Maybe artifact
  • Acanthocyte vs Echinocyte


Echinocyte (Burr Cell)






Howell-Jelly: are intracellular particles which are smooth, round remnants of nuclear chromatin (DNA. Usually, only one per cell is seen but, occasionally, there may be more than one
  • Megaloblastic anaemia
  • Mylodysplastic
Howell-Jolly Bodies



Heinz Bodies

Heinz Bodies

Cabot Rings



Cabot Rings



A – Cabot ring
B – Howell-Jolly body



Basophilic Stippling: is the term used to indicate the presence of irregular basophilic granules in the cytoplasm of erythrocytes. The granules are composed of unstable RNA and may be fine of coarse.
  • Lead Poisoning
  • Thalassaemia
  • Significant anaemia
  • Dyserythropoiesis
Basophilic Stippling


Hemoglobin C crystals:  are hexagonal crystals that may be found in individuals with HbC syndromes. The crystals may intracellular or extra-cellular.

Hemoglobin C crystals


Pappenheimer Bodies:  are intracellular inorganic iron-containing granules that may be ob-served on Wright’s stained peripheral blood smears.

Pappenheimer Bodies


Rouleaux formation: describes an aggregation of erythrocytes that are aligned one upon the other, resembling stacks of coins
  • High level of circulating acute-phase proteins.
  • with High ESR rate.
  • autoimmune conditions
  • myeloma
Rouleaux formation


Agglutination of red cells:  is caused by agglutinins and resembles Rouleaux but is more irregular with round clumps rather than linear Rouleaux







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