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Cellularity Information and Courses from MediaLab, Inc.

These are the MediaLab courses that cover Cellularity and links to relevant pages within the course.

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Laboratories Individuals

CLIA Hematology / Hemostasis Review
What is the normal cellularity of an iliac crest bone marrow biopsy in a 50 year old male:View Page

Introduction to Bone Marrow
Which of the following statements are FALSE regarding the bone marrow BIOPSY specimen?View Page
Match each of the following:View Page
Preparation of Particle Smears

Particle smears are also made from the unanticoagulated sample. The bone marrow particles are removed from the watchglass and placed on a coverslip. One of the following items: Pasteur pipet, capillary tube or broken end of a wooden applicator stick, may be used to transfer the particles. A second coverslip is placed over the first and the particles are crushed between the coverslips as they are pulled apart. Some practice is needed to perfect this technique. As mentioned previously, this type of preparation provides a more accurate assessment of marrow architecture and cellularity than the direct smear. Morphological detail is preserved on well made slides. The remaining sample may be added to a tube containing EDTA anticoagulant and additional smears may be made if needed.

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Preparation of Concentrated Smears

In some laboratories the anticoagulated sample is used to prepare concentrated smears. Placing the fluid in a Wintrobe tube and centrifuging it separates the sample into four layers:fat and perivascular cellsplasmabuffy layer - myeloid and nucleated erythroid cellserythrocytesThe volume of each layer is measured using the scale on the Wintrobe tube and then the percentage of each layer is calculated. Next the plasma is removed and a smear is made from the buffy coat and top of the red cell layer. Either the manual push method or cytospin technique may be used to make the smears. They may be stained with a variety of cytochemical stains. Concentrated smears are used to examine cell morphology and demonstrate the presence of abnormal cells when the marrow is hypocellular. The smears cannot be used for differential counts or evaluation of cellularity.

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Advantages of a Biopsy Specimen

Examining the biopsy allows the structure of the marrow to be viewed as it exists in the body. It provides essential diagnostic information in conditions that disrupt the normal architecture, such as metastatic carcinoma, myelofibrosis, Hodgkin's lymphoma and granuloma. A biopsy may also be used to evaluate cellularity and identify acid-fast bacteria or fungi in less time than is needed for routine culture methods. One disadvantage of the tissue sections prepared from the biopsy sample is that morphologic detail is lost. For this reason, in many cases imprint slides or smears from the aspirated sample are also examined.

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Which of the following statements are TRUE regarding biopsy specimens? (Choose ALL of the correct answers)View Page
Preparation of Direct Smears

The sample in the first syringe is quickly delivered into a watchglass or onto a slide. After the technologist verifies the presence of white-gray marrow particles in the sample, push smears and/or coverslip smears from this unanticoagulated sample are made immediately. All films should be rapidly air dried. The appearance of fat as irregular holes in the films also give the assurance that marrow and not just blood has been obtained. This type of smear is referred to as a direct smear and is usually used to evaluate morphology. Although some evaluation of cellularity and M:E ratio is possible, particle smears or biopsy sections provide a more accurate representation of these factors.

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Collection of Bone Marrow Biopsy

A bone marrow biopsy involves removing a small portion of the bone marrow without destroying the architecture of the marrow. This type of biopsy is necessary when the marrow cannot be aspirated (dry tap) due to a disease process, and also provides additional information complementary to that derived from the aspirate: biopsy specimens are more accurate for assessing cellularity, and infiltrative processes, such as metastatic carcinoma, fibrosis, amyloid, and lymphoma. A biopsy specimen is processed as follows: touch preparation tissue section

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The average bone marrow cellularity in a normal adult is:View Page
Percentages of Myeloid and Erythroid Precursors

The normal cellularity has been described as 50%. Therefore, about 40% of the cells would be myeloid (granulocytic) and 10% erythroid. Since cellularity and distribution may vary from one area of the marrow to another, an acceptable range for percentages of myeloid and erythroid cells would be:Myeloid cells 25-55%Erythroid cells 8-14%

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Representative Counting Field

The actual cell count is performed using the oil (100x) objective. This oil immersion field shows a representative counting field. Four granulocytes, a prorubricyte, and two rubricytes are completely visible here. 100 to 500 nucleated cells are generally counted,depending on the cellularity of the smear, and only cells completely visible in the field should be included in the count.

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Microscopic Evaluation of Marrow Smears

The microscopic examination of marrow smears can be divided into three main steps.Evaluating cellularity from the biopsy/particle smearEvaluating marrow iron from the biopsy/particle smearMorphology examination from the Romanwsky stained smears

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Medium Power View of Biopsy

This biopsy also has a cellularity of 25% and approximately 75% fat, and is therefore slightly hypocellular.

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Select the correct answer from the choices provided.View Page
Evaluating Cellularity

The biopsy section or particle smears are the preparations that are preferred for the evaluation of marrow cellularity and architecture. The low power objective is used to examine the slide and compare the cellular area to the amount of fat (fat cells appear as white circles interspersed among the cellular elements). On the biopsy section the specific type of cells present are difficult to determine but the cellularity can be clearly seen. The particle smear may be used to evaluate cellularity as well as morphology. The diagnostic significance of the evaluation of cellularity, is simply to see if there are too few, too many, or sufficient cell precursors present in the bone marrow.

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Example

An example of the clear space left by a fat cell when the marrow was aspirated from the bone. Some appreciation for marrow cellularity can be obtained by comparing the cells present versus the fat spaces seen in the more cellular areas of the smear.

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Hypercellular Bone Marrow Biopsy

This is another view of the same slide showing increased cellularity and decreased fat.

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Hypercellular Bone Marrow Biopsy

A low power view of a biopsy section stained with hematoxylin eosin stain. This section is showing increased cellularity and decreased fat. This specimen is about 85% cellular.

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Select the correct answer from the choices provided.View Page

White Cell and Platelet Disorders: Peripheral Blood Clues to Nonneoplastic Conditions
Normal Bone Marrow

Illustrated in the photograph is a normal bone marrow smear stained with Wright/Giemsa stain. Note the evenly distributed cells with normal maturation in both the myeloid and erythroid maturation sequences.An estimation of the percentage composition of cells can be made by experienced observers from scanning of multiple fields. In some instances a detailed differential count of 300 or more cells must be made.In normal bone marrows, the myeloid to erythroid ratio (M:E ratio)ranges from 1.2:1 to 5:1.A ratio of less than 1.2:1 indicates depressed leukopoiesis or erythroid hyperplasia. Ratios of 6:1 or greater usually indicates infection, erythroid hypoplasia, or chronic myelogenous leukemia.An assessment of the overall cellularity is also useful. In general, cellularity of less than 25% indicates hypoplasia; greater than 75% indicates hyperplasia.

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