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Howell-jolly bodies Information and Courses from MediaLab, Inc.

These are the MediaLab courses that cover Howell-jolly bodies and links to relevant pages within the course.

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CLIA Hematology / Hemostasis Review
The abnormal RBC indicated by the arrow in this illustration is indicative of:View Page
Identify the object contained in the cell in this illustration indicated by the arrow:View Page
Howell-Jolly bodies are composed of:View Page

Erythrocyte Inclusions - Wright Stained Smears
Single erythrocyte inclusions which are large, round, smooth and purplish-blue staining are most likely:View Page
Multiple dark blue particles of varying size scattered throughout the cytoplasm of erythrocytes is/are called:View Page
The erythrocyte inclusions which are thin, red-purple staining strands of varying shapes are called:View Page
A few dark blue staining granular inclusions located near the periphery of an erythrocyte are most likely:View Page
Degenerated erythrocyte cytoplasmic organelles which contain iron are:View Page
Remnants of erythrocytes nuclei, nuclear fragments, or aggregates of chromosomes which have separated from the mitotic spindle are:View Page
Match the names of the inclusions with their corresponding diagrams.View Page
The RBC that is indicated by the arrow containsView Page
What are Howell-Jolly Bodies?

Howell-Jolly bodies are round, smooth, almost pyknotic, dark purple bodies ranging in size from 0.5 to 1.0 micron in diameter. Located eccentrically, usually only one Howell-Jolly body occurs in a mature or nucleated erythrocyte. Occasionally, two or more Howell-Jolly bodies per cell may be found. These DNA inclusions demonstrate a positive Feulgen reaction which is specific for DNA and RNA.

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More on Howell-Jolly Bodies

Under normal conditions, Howell-Jolly bodies are thought to be remnants of nuclear fragments due to incomplete expulsion of the nucleus. In pathological conditions, they are aggregates of chromosomes which have separated from the mitotic spindle during abnormal mitosis. Single or multiple Howell-Jolly bodies may be found in a red cell. A single HJ body in a red cell may be seen in megaloblastic anemia, hemolytic anemia such as sickle cell anemia and after splenectomy. Megaloblastic anemia or abnormal erythropoiesis is usually present when multiple Howell-Jolly bodies are observed in a single cell.

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What is the composition of Howell-Jolly bodies?View Page
In which of the following conditions would you expect to find Howell-Jolly bodies?View Page
Howell-Jolly Bodies in Cytoplasm

Since Howell-Jolly bodies are nuclear remnants, they can also be seen in the cytoplasm of the young nucleated red cells.

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If present, how many Howell-Jolly bodies are usually seen within each erythrocyte?View Page
In a Wright's-stained smear, Pappenheimer bodies must be differentiated from basophilic stippling and Howell-Jolly bodies. Pick the statement which best describes each of the following.View Page
This smear shows:View Page
This Prussian blue stained smear shows:View Page
Comparison of Erythrocyte Inclusions

In section A of the image, the arrow points to an RBC with basophilic stippling.In section B, the arrows point to erythrocytes containing Pappenheimer bodies.The arrows are pointing to Howell-Jolly bodies in section C.By contrast, in section D the arrow is pointing to a platelet that is sitting on top of an RBC. This may be mistaken for an inclusion. One of the distinguishing characteristics that can alert you to the fact that it is not an inclusion is the halo around the platelet.

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Howell-Jolly Bodies contrasted with Pappenheimer Bodies.

Pappenheimer bodies are indicated with single arrows. A Howell Jolly body is shown at the double arrow.

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The smear several Howell-Jolly bodies as well as several _____________ bodies.View Page

Red Cell Disorders: Peripheral Blood Clues to Nonneoplastic Conditions
Match the form of red cell inclusions in each of the frames of photographs with a corresponding clinical condition.View Page
The red cell inclusions in this split frame photomicrograph of peripheral smears are called:View Page
What are the erythrocyte inclusions that are indicated by the arrows on this blood smear?View Page
Reticulocyte identification

Reticulocytes are red blood cells prematurely released from the bone marrow. On a Wright-Giemsa stained blood smear, they appear as polychromatic macrocytes. Their presence in the peripheral blood may suggest hemolysis or bleeding. Their presence is expressed as a percentage of the red cell count: newly born= 3-7%; up to one week of age=1-3%; >one week =0.3-1.8%. Automated or manual methods may be used to enumerate reticulocytes. In clinical context, retics must be separated from debris, precipated stain, Pappenheimer bodies, Howell-Jolly bodies, and Heinz bodies.

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The RBC inclusions shown in the photograph represent which of the following?View Page
The peripheral blood smear represented by this field was submitted for hematologic review. The RBC inclusions most likely are:View Page
Hemolytic disease of the newborn

Jaundice was recognized in a day-old infant. Notice particularly the size variation (anisocytosis) of the erythrocytes on the infant's peripheral smear. What does this observation mean? Does it provide immediate information that might serve as guidance in expediting diagnosis and treatment? Note that normal-sized red blood cells, microcytes, microspherocytes, macrocytes, and nucleated red blood cells are all present. Red cell variations are expected findings in healthy neonates, but the variations here are exaggerated. Hyposplenic functional features may appear, including acanthocytes, spherocytes, and possibly Howell-Jolly bodies, especially if hemolysis is particularly vigorous. A high (3-7%) reticulocyte count is not unusual during the first three or four days after birth, however, the marrow in this jaundiced infant is proliferating vigorously in response to hemolysis. A call for more red cells is urgent. Immature red cells (in the form of nucleated red cells) and red cells with stippling of RNA (basophilic stippling) are readily identified. Red cell maturation sequence has not been totally processed in the marrow nor is all residual red cell debris removed by the spleen. In the lower photograph are reticulocytes stained by supravital stain (new methylene blue). Basophilic stippling (specks of RNA) stains with both supravital stains and with routine Wright-Giemsa stain.

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Guidelines for standard reports

In a study on the reporting of red blood cell morphology abnormalities conducted in Ontario, Canada (Hookey L, Dexter D, Lee DH, Laboratory Hematology 7:83-88, 2001), fewer than 50% of 33 participants used the same term to describe the quantitative frequency of peripheral blood abnormalities. Seven blood smears, each containing one of several abnormal erythrocytes-- schistocytes, teardrop cells, acanthocytes, and Howell-Jolly bodies--were evaluated by 32 participants. The participants were asked to document their evaluations from a list of quantitative terms. There was a heterogeneity in the use of terms "rare," "slight," "occasional," "few," "mild", "present," "moderate," "many," and "marked." Choices of terms were subjective without points of reference. Guidelines for establishing standardized qualitative estimations of abnormal erythrocytes in the peripheral smear are presented as follows: 1+ = 2 - 4/Oil Immersion Field (OIF) 2+ = 5 - 7/OIF 3+ = 8 - 10/OIF 4+ = >10/OIF. The terms "few," "moderate," "many," and "marked" may be substituted for the 1+ - 4+ grading system, but only when their specific points of reference are universally understood in tandem with the above guidelines. A comment should be triggered if any erythrocyte abnormalities are seen in numbers >3/OIF including, but not limited to, polychromasia, basophilic stippling, nucleated RBC's, and Howell-Jolly bodies. Rouleaux or RBC agglutination are important findings and must be documented.

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Normoblasts

Many of the distorted erythrocytes displayed on the previous page are also present on this one. We see anisocytosis, poikilocytosis, fragmented forms, target cells, and a few Howell-Jolly bodies. Note also circulating nucleated red blood cells (normoblasts). The presence of these normoblasts may represent a premature release from a hyperplastic marrow or, more likely, are due to a lessening of the normal inhibition of erythroid release from the marrow as a result of splenectomy, permitting their earlier entry into the circulation.

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Howell -Jolly bodies/ other erythrocyte environmental alterations

Several erythrocyte abnormalities are present in both the upper and lower photomicrographs. Many of these atypical cells are probably present as a result of the patient's splenectomy. Considerable anisocytosis and poikilocytosis with many tear-drop cells, bite cells, fragmented forms, and a few target cells are apparent. Some of the erythrocytes in the upper frame contain Howell-Jolly bodies (DNA fragments) that may be single or multiple, especially in myeloproliferative disorders. These inclusions stain negatively for iron and are eccentrically placed in the red cell cytoplasm. .

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