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ASH Image Bank (2007); doi:10.1182/ashimagebank-2007-7-00013
Copyright © 2007 by the American Society of Hematology.
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Atlas Image Set

Pappenheimer Bodies in Sickle Cell Disease

John Lazarchick, M.D.


Figure 1
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Figure 1. A 26-year-old AF male with sickle cell disease who presented to the ER complaining of abdominal pain. His CBC at that time showed a hemoglobin of 7.2g/dL, WBC of 11.2k/uL and a platelet count of 360k/uL. His peripheral smear is show. Sickle cells are readily identified (intermediate-sized arrow) throughout the smear. A RBC with a Howell-Jolly body (small arrow) is also noted. Multiple irregular inclusions (large arrow) are present in many of the other RBC. These iron-containing granules are Pappenheimer bodies. A Prussian Blue is needed to confirm the presence of non-heme iron in these granules. Also note on this smear increased polychromatophilic cells and target cells.

 

Figure 2
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Figure 2. At a higher magnification, many of the RBCs can be seen to contain single or multiple irregular granules (small arrow). The larger arrow shows a typical sickle cell.

 

Figure 3
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Figure 3. This image best illustrates the difference between Pappenheimer bodies and Howell-Jolly bodies. The large arrow depicts a RBC with a Howell-Jolly body. Note: this is a single round dense structure with a regular border, as opposed to the Pappenheimer bodies (small arrow), which are frequently multiple inclusions with irregular borders. Howell-Jolly bodies are fragments of DNA and typically seen in the peripheral smears of individuals with sickle cell disease following auto-splenectomy. A nucleated RBS is also present in this view.

 

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Related ASH-SAP Chapter:space logo
Chapter 6: Hemolytic anemias

This Article
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PubMed
Right arrow Articles by Lazarchick, J.
Related Collections
Right arrow Hemolytic Disorders
Right arrow Iron and Blood Loss
Right arrow Related ASH-SAP Chapter
Right arrowRelated Image Bank Image Sets
Right arrowRelated ASH Education Book Articles
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Copyright © 2007 by the American Society of Hematology.