Haematological Conditions 1
Dr A McLeod

Back to Main Page


Abnormal erythrocytes:
Abnormal erythrocytes:



Erythrocyte Abnormalities

Erythrocyte
Normal Erythrocyte (red cell)
  • 6-8 micrometres diameter, 2 micrometers thick
  • Biconcave shape with lighter-appearing cytoplasm centrally and (usually) no granules.
  • No nucleus
  • Common - approx 4-6 million / mm3 blood
See below left for abnormal erythrocytes - the most important for undergrad exams are in red text.

Abnormal erythrocytes
Abnormal Erythrocytes



Bite Cells
Bite Cells (arrowed)
  • Hypochromic microcytic erythrocytes: occur in certain types of anaemia including iron deficiency anaemia and thallasaemia. They are smaller than normal erythrocytes, usually <6 micrometers diameter.
  • Macrocytes are larger than normal erythrocytes occurring in certain types of anaemia including those caused by B12 or folate deficiency (and others listed here).
  • Normoblasts (or erythroblasts): are the immediate precursors of erythrocytes - at this stage the nucleus is retained as can be seen in the illustration. There are four stages of development.
  • Spherocytes: are red cells with a loss of membrane leading to reduced diameter and decreased surface area but normal volume. They are seen in hereditary spherocytosis, erythroblastosis fetalis and acquired hemolytic anemias. 
  • Stomatocytes: erythrocytes with a loosely folded, mouth-like pale area across the cell. They are seen in hereditary stomatocytosis, lead poisoning and thalassemia trait. 
  • Target cells (or codocytes): have the hemoglobin concentrated in the middle and the periphery of the cell, and thereby resemble targets. They can be seen in hemoglobinopathies, e.g. thalassemias, and iron deficiency anemia. 
  • Teardrop erythrocytes (or dacryocytes): are seen when there is extramedullary erythropoiesis or with marrow disorders or marrow infiltration, such as myelofibrosis or metastatic carcinoma
  • Elliptocytes: occur with several inherited disorders predisposing to haemolytic anaemia They can also be seen in acquired disorders, such as iron defiency anemia, infectious anemias, thalassemia, and in newborn babies. 
  • Sickle cells: are seen in sickle cell anaemia - an autosomally inherited disorder.
  • Acanthocytes: are spherocytical cells with large irregularly placed protrusions.
  • Echinocytes: are red blood cells distorted by exposure to a hypertonic medium.
  • Schizocytes (schistocytes or helmet cells): are fragmented cells showing bizarre poikilocytosis. They can be seen in various forms of microangiopathic haemolytic anemia as well as after injury by mechanical means, e.g. through cardiac valve prostheses. 
  • Bite cells: are indicative of some haemolytic anaemias (e.g. G6DP deficiency). They occur when there is a precipitation of haemoglobin against a portion of the inner membrane (known as a Heinz Body). This is later removed in the spleen leaving a 'bite mark'. Other causes of Heinz bodies (and thus Bite cells) are oxidant drugs and haemolytic anemia associated with severe liver disease. Not all bite cells are as evenly shaped as shown in the top pic - see separate illustration)
  • Howell-Jolly bodies: are the small dark bodies in the illustration. They are nuclear remnants which are present in some normal red cells in the bone marrow but are removed by the spleen during the first few hours the cells spend in the circulatation. This appearance results from absence of splenic function, either following splenectomy, or occasionally due to splenic atrophy.
  • Basophilic stippling: of erythrocytes occurs with lead poisoning or megaloblastic anaemia. In this latter case the erythrocytes may be nucleated. Other causes here.


PATHOLOGYPHARMACOLOGYMAIN PAGELINKSiBSc

Updated March 2010



References
Abnormal red blood cells
Cell morphology