Which of the following conditions is associated with the presence of spherocytes?

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The presence of spherocytes is primarily associated with hereditary spherocytosis. This condition is a genetic disorder characterized by a defect in the red blood cell membrane, leading to the formation of spherically shaped red blood cells rather than the normal biconcave disk shape. These spherocytes are less stable and more prone to hemolysis, especially in the spleen, resulting in anemia and jaundice.

In hereditary spherocytosis, the abnormality in the red blood cell membrane is often due to defects in proteins such as ankyrin, spectrin, or band 3 protein. As a result, patients may exhibit signs of hemolytic anemia, including elevated bilirubin levels, increased lactate dehydrogenase, and decreased haptoglobin. The presence of spherocytes can be seen on a peripheral blood smear, which is one of the key diagnostic features for this condition.

Other conditions listed, like aplastic anemia, sickle cell disease, and thalassemia, do not typically present with spherocytes. Aplastic anemia is characterized by a reduction in all blood cell types due to bone marrow failure. Sickle cell disease leads to the formation of sickle-shaped red blood cells due to abnormal hem

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