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Hb SC disease
Double heterozygous condition where an abnormal sickle gene from one parent and abnormal C gene form the other parent is inherited
Echinocytes (Burr cells)
Type of cells seen in:
Liver disease
Uremia
Heparin therapy
Pyruvate kinase deficiency or as an artifact.
Caused by changes in osmotic pressure
Moth-eaten look
Water or drying artifacts can give what type of appearance to RBCs?
Acanthocytes
Type of cells caused by excessive cholesterol in the membrane
Associated with:
Alcoholic liver disease
Post-splenectomy
Abetalipoproteinemia
Target cells
Type of cells that show central areas of hemoglobin surrounded by a colorless ring and a peripheral ring of hemoglobin; have an increased surface-to-volume ratio
Seen in:
Liver disease
Hemoglobinopathies
Thalassemia
Iron deficiency anemia
Spherocytes
Disk-shaped cells with a smaller volume than a normal erythrocyte
Cells have a decreased surface to volume ratio
Lack of a central pallor area
Pyropoikilocytes
Type of cells frequently seen in burns
Dacrocytes
Pear-shaped cells with one blunt projection
Seen in megaloblastic anemia, thalassemias, and extramedullary hematopoiesis (myelofibrosis, myelophthisic anemia)
Helmet cells
Type of cells seen in microangiopathic hemolytic anemias (MAHA)
Schistocytes
Damaged RBC; fragments of various sizes and shapes are present, often with pointed projections
Seen in microangiopathic hemolytic anemia (MAHA)
Thermal injury
Renal transplant rejection
G6PD deficiency
Stomatocytes
Type of cells characterized by an elongated or slit-like area of central pallor
Seen in liver disease, hereditary stomatocytosis or as artifact
Caused by osmotic changes due to cation imbalance (Na+, K+)
Elliptocytes
Cigar to egg-shaped erythrocytes associated with defects of the red cell membrane proteins
Nucleated RBCs
RBC inclusion that is usually an orthochromatic normoblast but can appear in any erythropoeitic stage of maturation
Indicates bone marrow stimulation or increased erythropoiesis
Howell-Jolly Bodies
Small round DNA fragments seen in sickle cell anemia, beta thalassemia major and other severe hemolytic anemias, megaloblastic anemia, alcoholism, and post-splenectomy
Basophilic Stippling
Multiple, tiny, fine and coarse inclusions evenly dispersed thoughout the cell
It has a “blueberry bagel” appearance
Pappenheimer Bodies
Small, irregular, dark staining, iron granules usually clumped together at periphery of the cell
Caused by an accumulation of ribosomes, mitochondria, and iron fragments
Cabot rings
Thin- red-violet, single to multiple ring-like structures that may appear in loop of figure-eight shapes
Seen in megaloblastic anemia, myelodysplastic syndromes, lead poisoning
Heinz bodies
Degraded hemoglobin usually seen in G6PD deficiency