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20             Part I:  Clinical Evaluation of the Patient                                                                                                                        Chapter 2:  Examination of Blood Cells            21




                    MORPHOLOGIC EXAMINATION                           film interpretation. For example, leukemic blasts may appear dense
                                                                      and rounded and lose their characteristic features when viewed in the
                  OF THE BLOOD                                        thick part of the film. For specific purposes, the thick portion or side
                                                                      and “feathered” edges of the film are of interest (for instance, to detect
               Microscopic examination of the blood spread on a glass slide or cover-  microfilariae and malarial parasites or to search for large abnormal cells
               slip yields useful information regarding all the cells of the blood. The   and platelet clumps).
               process of preparing a thin blood film causes mechanical trauma to the   The blood film is first scanned at low magnification (×200) to confirm
               cells, introducing artifacts that can be minimized by good technique.   reasonably even distribution of leukocytes and to check for abnormally
               The optimal part of the stained blood film to use for morphologic   large or immature cells in the side and feathered edges of the film. The
               examination of the blood cells should be sufficiently thin that a small   feathered edge is examined for platelet clumps. Abnormal cells, red cell
               proportion of erythrocytes in a ×1000 magnification field touch each   aggregation or rouleaux, background bluish staining consistent with para-
               other, but not so thin that no red cells are touching. Figure 2–4 is a   proteinemia, and parasites are all findings that can be suggested by medium
               composite image taken from the optimal portion of the film showing   magnification examination (×400). The optimal portion of the film is then
               the five major leukocyte types, normal red cells, and platelets. Selection   examined at high magnification (×1000, oil immersion) to systematically
               of a portion of the blood film for analysis that is too thick or too thin   assess the size, shape, and morphology of the major cell lineages.
               for proper morphologic evaluation is the most common error in blood

























                     A                                B                               C






















                     D                                E                               F

               Figure 2–4.  Images from a normal blood film showing major leukocyte types. The red cells are normocytic (normal size) and normochromic (nor-
               mal hemoglobin content) with normal shape. The scattered platelets are normal in frequency and morphology. A. A platelet caught sitting in the
               biconcavity of the red cell in the preparation of the blood film. This normal finding should not be mistaken for a red cell inclusion. Images are taken
               from the optimal portion of the blood film for morphologic analysis. Image shows a (A) segmented (polymorphonuclear) neutrophil and in the inset
               a band neutrophil; (B) monocyte; (C) small lymphocyte; (D) large granular lymphocyte, note larger size than lymphocyte in (C) and increased amount
               of cytoplasm containing scattered eosinophilic granules; and (E) eosinophil. Virtually all normal blood eosinophils are bilobed and filled with relatively
               large (compared to the neutrophil) eosinophilic granules. F. Basophil and in inset a basophil that was less degranulated during film preparation,
               showing relatively large basophilic granules. The eosinophilic and basophilic granules are readily resolvable by light microscopy (×1000), whereas the
               neutrophilic granule is not resolvable but in the aggregate imparts a faint tan coloration to the neutrophil cytoplasm, quite distinctly different from
               the blue-gray cytoplasmic coloring of the monocyte and lymphocyte.






          Kaushansky_chapter 02_p0011-0026.indd   20                                                                    17/09/15   5:35 pm
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