Veterinary Hematology
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Veterinary Hematology

Atlas of Common Domestic and Non-Domestic Species

William J. Reagan, Armando R. Irizarry Rovira, Dennis B. DeNicola

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eBook - ePub

Veterinary Hematology

Atlas of Common Domestic and Non-Domestic Species

William J. Reagan, Armando R. Irizarry Rovira, Dennis B. DeNicola

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Now in its third edition, Veterinary Hematology: Atlas of Common Domestic and Non-Domestic Species continues to offer veterinarians and veterinary technicians an essential guide to veterinary hematology. Comprehensive in scope, the atlas presents the fundamentals of both normal and abnormal blood cell morphologies, with coverage of a wide range of species, including dogs, cats, horses, ruminants, llamas, rats, mice, nonhuman primates, ferrets, rabbits, guinea pigs, birds, amphibians, and reptiles.

Designed as a useful and accessible guide, the updated third edition presents more than 300 color images and includes a new chapter that describes the best techniques for using hematology instruments.The authors—noted experts on the topic—clearly show how to identify and interpret the hematological changes that may occur in a variety of species. In addition, a companion website offers a wealth of additional hematological images. This vital atlas:

  • Provides an updated edition of the popular veterinary hematology atlas for veterinarians, veterinary students, and veterinary technicians
  • Contains a new instructive chapter on hematology instrumentation
  • Presents hundreds of high-quality color photographs that help in identification
  • Covers a range of species from dogs and cats to birds and reptiles
  • Features a companion website that provides a wealth of hematological images

Written for both novice and experienced veterinarians, Veterinary Hematology provides a complete resource to blood morphologic abnormalities in domestic and non-domestic species.

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Información

Año
2019
ISBN
9781119064978
Edición
3
Categoría
Medicine

CHAPTER ONE
Hematopoiesis

General Features

All blood cells have a finite life span, but in normal animals, the number of cells in circulation is maintained at a fairly constant level. To accomplish this, cells in circulation need to be constantly replenished, which occurs via the production and release of cells from the bone marrow. Production sites in the bone marrow are commonly referred to as medullary sites. In times of increased demand, production can also occur outside the bone marrow in sites such as spleen, liver, and lymph nodes. These sites are called extramedullary sites. In rodents, in the normal steady state, extramedullary production of blood cells occurs in the spleen.
Hematopoiesis, the production of blood cells, is a complex and highly regulated process. Some differences in hematopoiesis exist between species and are beyond the scope of this text; readers are referred to the detailed coverage in some of the references in Bibliography section. The dog will be used to demonstrate some of the basic principles of hematopoiesis. All blood cells in the bone marrow arise from a common stem cell. This pluripotent stem cell gives rise to several stages of committed progenitor cells, which then differentiate into cells of the erythrocytic, granulocytic, megakaryocytic, and agranulocytic (monocytic and lymphocytic) lineages. The end result of this development process is the release of red blood cells, white blood cells, and platelets into the circulation. At the light microscopic level, without the use of immunocytochemistry or enzyme cytochemistry, it is impossible to accurately identify the early stem cells in the bone marrow, but the more differentiated stages of development can be identified and are graphically depicted in Figure 1.1.
An overview of hematopoiesis with the graphical representation of more differentiated stages of development. Successive arrows lead from Pluripotent stem cell to Myeloid stem cell, Rubriblast, Prorubricyte, Rubricyte, Metarubricyte, Polychromatophil, and to RBC. An  arrow leads from Pluripotent stem cell to Lymphoid stem cell, from where two arrows lead to B lymphocyte and T lymphocyte, respectively. From Myeloid stem cell, successive arrows lead to Megakaryoblast, Promegakaryocyte, Megakaryocyte, and to Platelets. Another arrow from Myeloid stem cell leads to Monoblast, from there to Promonocyte, and then to Monocyte. From Myeloblast an arrow points to Promyelocyte from where three series of subbranches are formed using successive arrows. The first one has Eosinophilic myelocyte, Eosinophilic metamyelocyte, Eosinophilic band, and Eosinophil. The second series contains Neutrophilic myelocyte, Neutrophilic metamyelocyte, Neutrophilic band, and Segmented neutrophil. The third series includes Basophilic myelocyte, Basophilic metamyelocyte, Basophilic band, and Basophil.
Figure 1.1 Overview of hematopoiesis.
Figure 1.2 shows a histological section of a bone marrow core biopsy from an adult dog. Note that there is a mixture of approximately 50% hematopoietic cells and 50% fat that is surrounded by bony trabeculae. The specific types of bone marrow cells can be difficult to recognize in histological sections at this low-power magnification, but the very large cells present are megakaryocytes. Cells are easier to identify on a smear from a bone marrow aspirate (Figure 1.3). The cells that are present include erythrocytic and granulocytic precursors and a megakaryocyte. To classify these three different cell types, there are some general features that can be used. Megakaryocytes are easy to distinguish by their very large size; the majority of them are 100–200 μm in diameter compared with approximately 20–30 μm for the largest granulocytic or erythrocytic precursors.
10 times magnification of Canine bone marrow core biopsy using hematoxylin and eosin stain. There are pink bony trabeculae in the lower left corner, lower right corner, and top of the photomicrograph, and surrounding the hematopoietic cells and fat. There are round to oval clear areas indicating the fat. there are also many small, round purple structures, indicating the erythrocytic and granulocytic precursor cells. The larger, densely staining purple structures distributed throughout the marrow space are megakaryocytes.
Figure 1.2 Histological section of canine bone marrow. Pink bony trabeculae are present in the lower left corner, lower right corner, and top of the photomicrograph and surround the hematopoietic cells and fat. The round to oval clear areas are the fat. The erythrocytic and granulocytic precursor cells are the many small, round purple structures. The larger, densely staining purple structures distributed throughout the marrow space are megakaryocytes. Canine bone marrow core biopsy; hematoxylin and eosin stain; 10× objective.
50 times magnification of canine bone marrow smear showing megakaryocyte, erythrocytic precursors, and granulocytic precursors. The megakaryocyte is the largest cell located in right center of the field. The early erythrocytic precursors have central round nuclei and deep blue cytoplasm. The early granulocytic precursors have oval to indented nuclei and blue cytoplasm. There is a granulocytic predominance in this field.
Figure 1.3 Megakaryocyte, erythrocytic precursors, and granulocytic precursors. The megakaryocyte is the largest cell located in right center of the field. The early erythrocytic precursors have central round nuclei and deep blue cytoplasm. The early granulocytic precursors have oval to indented nuclei and blue cytoplasm. There is a granulocytic predominance in this field. Canine bone marrow smear; 50× objective.
Cells of the erythrocytic lineage can be initially distinguished from those of the granulocytic lineage on the basis of their nuclear shape and color of cytoplasm (Figures 1.4 and 1.5). Cells of the erythrocytic lineage have very round nuclei throughout most stages of development. In contrast, the nuclei of cells of the granulocytic lineage become indented and segmented as they mature. In addition, the cytoplasm of early erythrocytic precursors is much bluer than that of the granulocytic precursors.
100 times magnification of canine bone marrow smear showing erythrocytic precursors. The majority of the intact cells present are early erythrocytic precursors with centrally located round nuclei and deep blue cytoplasm. The cells with round eccentrically placed nuclei and reddish blue cytoplasm are late-stage erythrocytic precursors. The largest cell in the right center of the field that has small pink granules in the cytoplasm is a promyelocyte.
Figure 1.4 Erythrocytic precursors. The majority of the intact cells present are early erythrocytic precursors with centrally located round nuclei and deep blue cytoplasm. The cells with round eccentrically placed nuclei and reddish blue cytoplasm are late-stage erythrocytic precursors. The largest cell in the right center of the field that has small pink granules in the cytoplasm is a promyelocyte. Canine bone marrow smear; 100× objective.
100 times magnification of canine bone marrow smear showing granulocytic precursors. The majority of the intact cells present are granulocytic precursors with oval to indented nuclei and blue cytoplasm. The larger immature forms have small, pink cytoplasmic granules. The cytoplasm becomes less blue as the cells mature.
Figure 1.5 Granulocytic precursors. The majority of the intact cells present are granulo...

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