Hematology
By Henry
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About this ebook
6-page laminated reference guide includes:
- Hematopoiesis/Hemopoiesis
- Organs of the Lymphatic System
- Blood
- Components
- Hemostasis
- Blood Groups
- ABO System
- RH System
- Specimen Collection
- Laboratory Assessment of Blood Formation & Disorders
- Abnormal Blood Cell Morphology
- Blood Disorders (over 2 full pages)
- NCLEX – great for reviewing hematologic disorders leading up to the exam
- Students – a very lightweight, inexpensive tool for boosting grades that can be slipped between your notebook pages for quick and easy answers
- Medical Professionals – great tool to have handy for a memory jog for you or as a nursing station reference for the team
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Book preview
Hematology - Henry
Table of Contents
WHAT IS HEMATOLOGY?
HEMATOPOIESIS/HEMOPOIESIS
ORGANS OF THE LYMPHATIC SYSTEM
BLOOD
SPECIMEN COLLECTION
BLOOD GROUPS
LABORATORY ASSESSMENT OF BLOOD FORMATION & DISORDERS
ABNORMAL BLOOD CELL MORPHOLOGY
BLOOD DISORDERS
WHAT IS HEMATOLOGY?
The study (morphology, physiology, and pathology) of blood and bloodforming organs and the diseases thereof
Uses:
As part of a routine medical exam to assess overall health
Diagnosis (e.g., an infection, anemia, or leukemia)
Monitoring of a condition and its treatment
HEMATOPOIESIS/HEMOPOIESIS
The formation of blood cells and platelets. In a fetus, formation starts in the yolk sac, moves to the liver and spleen, and then moves to the bone marrow. In an infant, formation occurs in the bone marrow, which is present in almost all bones. In an adult, formation of red and most white blood cells and platelets occurs in the marrow of the proximal ends of the femur, pelvis, sacrum, vertebrae, ribs, sternum, and skull
Hemopoietic growth factors: Erythropoietin (EPO), FLT3 ligand (FLT3-L), granulocyte colony-stimulating factor (G-CSF), granulocyte-macrophage CSF (GM-CSF), interleukin-1 (IL-1), IL-3, IL-5, IL-6, macrophage-CSF (M-CSF), stem cell factor (SCF), thrombopoietin (TPO), tumor necrosis factor (TNF), and vascular endothelial growth factor (VEGF). Effects are mediated by binding receptors on cell surfaces
Hemopoietic stem cell: Pluripotent, rare (frequency is 1 per 20 million nucleated cells in bone marrow) CD34+CD38-Lin- phenotype. Gives rise to more than 106 mature cells after 20 cell divisions and can self-renew by asymmetric cell division
Hemopoietic progenitor cell: Multipotent
Erythropoiesis: Formation of red blood cells (RBCs); regulated by EPO, which is secreted by the kidneys in response to hypoxia (oxygen tension, the partial pressure of oxygen)
Stem cell → progenitor cell → colony-forming unit (CFU) granulocyte, erythroid, monocyte, and megakaryocyte (GEMM) (CFUGEMM ) → burst-forming unit (BFU) erythroid (E) (BFUE) → CFUE → pronormoblast → series of normoblasts in marrow that decrease in size, increase in hemoglobin (Hb) content, lose RNA+ protein synthesis apparatus, and increase chromatin condensation → reticulocyte (nucleus extruded; nuclear DNA lost), which contains some ribosomal RNA (rRNA) and synthesizes Hb → mature erythrocyte (rRNA lost), which is a non-nucleated, bi-concave disc (i.e., cell-like)
Assess by Hb level, reticulocyte count, and bone marrow exam
Total erythropoiesis assessed by the cellularity of marrow and myeloid:erythroid ratio
Effective erythropoiesis assessed by reticulocyte count
Ineffective erythropoiesis: ~10–15% of erythroblasts die in bone marrow; increases in some chronic anemias; associated with increased unconjugated bilirubin (derived from the breakdown of Hb) and lactate dehydrogenase LDH (derived from breakdown of cells) in serum
Extramedullary hematopoiesis (EMH): Formation and development of blood cells outside bone marrow in response to the failure of erythropoiesis in bone marrow