Wintrobe's Clinical Hematology 14e SC
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Part 1: Laboratory Hematology— SECTION 1
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FIGURE 1.6 Bone marrow core biopsy. Histologic preparation of the bone marrow core biopsy following fixation and decalcification. The biopsy is stained with hematoxylin and eosin. This preparation allows for optimal evaluation of bone marrow cellularity and interaction of bone marrow cells with bony trabeculae and
is helpful in evaluating extrinsic features, such as metastatic tumor or fibrosis in the marrow. Panel A (low power) showing bony spicules and marrow in section of
bone marrow core biopsy. Panel B (high power) showing morphologic detail of hematopoietic tissue within the section.
oil immersion magnification in most marrows. Only intact cells are
to give an approximation of the size of the bone core within the needle.
evaluated; all bare nuclei are excluded. Counting is performed in an
The biopsy needle is rotated and gently rocked to free the biopsy from the
surrounding bone and then advanced slightly farther. The biopsy is then
area where few bare nuclei are present and the cells are not overlapping,
removed from the bone by withdrawing the needle, and slight positive
found in clusters, or artifactually distorted because of the spreading
pressure may be applied using a syringe. The biopsy is expressed from
artifact. This is usually in the dispersed cell zone adjacent to the spicule.
the needle by the stylet. Touch preparations of the bone biopsy should
It should be noted that spicules may be absent in pediatric marrows
be made, particularly if no aspirate was obtained, to allow cytologic
where marrow cells will be uniformly dispersed. Reference ranges
examination of the bone marrow elements. The bony core is then fixed, decalcified, and processed for histologic examination. 113,114 Ancillary
for the percentage of bone marrow cell types vary widely between
laboratories and are used only as guides for what is to be expected in normal bone marrow samples 111 (for example of reference ranges,
testing can often be performed on additional bone marrow cores when
see Table 1.3 ). The proportions of each cell type and progression of
no material can be aspirated, so collection of more than one core biopsy
may be necessary.
the maturational sequence for myeloid and erythroid elements are
Once the biopsy is completed, manual pressure is applied to the site
determined from the differential counts. In addition, the myeloid to
for several minutes to achieve hemostasis. The site is then bandaged,
erythroid ratio may be calculated.
and the patient is instructed to remain recumbent so as to apply further
Differences in cell differential results among infants, children, and adults exist ( Table 1.4 ). 108,111,113,115 In general, lymphocytes are more
pressure for approximately 30 to 60 minutes. If a patient is thrombo-
cytopenic, pressure bandages should be applied and the site checked
commonly seen in the marrow of children, especially those younger
frequently for prolonged bleeding.
than 4 years, where they may compose up to 40% of the marrow cellularity. 116 Plasma cells are rare in the marrow of infants and chil- dren. Lymphocytes are much less numerous in adult bone marrows, < 20% of adult marrow cellularity. Lymphocyte and plasma cell counts in adults tend to be quite variable, perhaps usually making up
Staining and Evaluation of Bone Marrow Aspirates and Touch Preparations
The bone marrow aspirate or touch preparation slides are stained with
reflecting the tendency of these cells to be unevenly distributed in the
either Wright or May-Grünwald-Giemsa stains, similar to blood smears.
bone marrow of adults. Often, lymphoid cells are found in nodular
These stains allow excellent morphologic detail and allow differential
aggregates in older adults, and plasma cells tend to be associated with blood vessels. 117 During the first month of life, bone marrow erythroid cells are prom- inent because of high levels of erythropoietin 118 ; thereafter, the erythroid
counts to be performed. Unstained smears should be retained for possible special stains if indicated. 108,111
Evaluation of bone marrow aspirates gives little information about
the total cellularity of the bone marrow because of fluctuations in cell
cells make up 10% to 40% of the marrow cells. Relatively few early
erythroid precursors (normoblasts) are usually seen, and more mature
counts induced by peripheral blood contamination of the bone mar-
row specimen and preparation artifacts. An overall impression of the
forms predominate. Erythroid cells should be examined for abnormalities
cellularity may be given (ie, cellular or paucicellular). More accurate
in morphology as well as iron content because these features are often
evaluation of bone marrow cellularity requires examination of the bone
deranged in pathologic states. Myeloid cells are usually the predominant
marrow biopsy or particle clot section, although the biopsy represents
bone marrow element, and more mature cells predominate over immature
a tiny fraction of the total marrow and may also be subject to sampling error. 108,113 The stained aspirate smear will have a central zone of dark
myeloblasts. Children tend to have higher numbers of eosinophils and
eosinophilic precursor cells than do adults, although many medications,
Copyright © 2019 Wolters Kluwer, Inc. Unauthorized reproduction of the content is prohibited. marrow particles and stroma surrounded by a thinner area of dispersed bone marrow cells and red cells (Figure 1.5). Low-power examination allows evaluation of the adequacy of cellularity and of the presence of allergies, or infections may increase the bone marrow eosinophil count. Megakaryocytes constitute the least abundant cell type seen in the bone marrow, usually making up
< 1% of the cells. 108 In addition to the hematopoietic cells, a variety of other cells may
megakaryocytes. Infiltrating tumor cells or granulomas may also be seen by scanning the aspirate smear at low power. 111
be seen in bone marrow aspirates in varying proportions, including
The aspirate smear allows cytologic examination of the bone marrow
macrophages, mast cells, stromal cells, and fat cells. In children, os-
teoblasts and osteoclasts may be seen, although these cells are rare in
cells. A minimum of 500 nucleated cells should be evaluated under
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