Hematology
Hematology
Hematology
• The study of blood and blood forming organs
Hematopoiesis
• The process through which pluripotent stem cells differentiate into various types of blood cells.
• Before birth, this happens in spleen, liver, lymph nodes, and thymus
• After birth, happens in bone marrow
Blood Volume
• 6% of total body weight• Body can compensate for .5 liters blood loss• Fluid shift can easily alter amount of blood• Number of red blood cells remain constant• Red blood cells confined to vascular space
Blood Components
• Plasma• Red blood cells• White blood cells • Platelets
Plasma
• 90-92 % water• 6-7% proteins• Large proteins (Albumin) won’t cross
membranes• Osmotic Pull (Oncotic pressure)- water
retention
Erythropoietin
• Hormone responsible for red blood cell production
Red Blood Cells
• Erythrocyte- red blood cell• No nucleus when mature
Hemoglobin
• Oxygen-bearing molecule in RBC• Made up of iron-rich pigment- heme and
protein- globin• Each hemoglobin has 4 subunits of globin• Each globin can carry one Oxygen molecule
Oxygen Transport
• Normal pO2 is 95 mmHg• Bohr effect- Uptake of O2 in lungs:• Alkalosis makes hemoglobin bind to oxygen
more tightly• Acidosis makes hemoglobin release oxygen
Erythropoeisis
• Production of red blood cells
Hemolysis
• Destruction of red blood cells
Lab Values H&H
• Hematocrit - Packed red cell volume• Normal 40 -52%• Hemoglobin• Normal 12 – 15 g/dL for males• Normal 10.5-14.0 g/dL for females
White Blood Cell Production
• Leukopoiesis (differentiation of WBC)• Immature WBC:– Myeloblasts– Monoblasts– Lymphoblasts
White Blood Cells
• Granulocytes• Monocytes• Lymphocytes
Granulocytes
• Basophils- primary function in allergic reaction… contain histamine….
• Eosinophils-Fight parasitic infection… can counteract allergic reactions
• Neutrophils- count can rise rapidly… fight infection
Monocytes
• May circulate as monocytes or mature into “Macrophages”
• Garbage collectors
Lymphocytes
• Primary cells involved in immune response• T- Cells (thymus)• B- Cells (bone marrow)
Autoimmune Disease
• Condition in which the body makes antibodies against own tissues
Inflammatory Response
• Nonspecific defense mechanism that wards off damage from microorganisms or trauma
White Blood Cells
• Leukocytes• Many (marginalized) loiter on walls of blood
vessels.• Demargination- recirculation of WBC in
response to stress, corticosteroids, seizures, epinephrine, and exercise
Phagocytosis
• When white blood cells engulf and destroy an invader
Platelets
• Throbocytes• 150,000 – 450,000 per microliter of blood• Live 7 – 10 days• Removed by the spleen• Thrombocytosis – too many
Hemostasis
• Vascular Spasms• Platelet Plug• Stable Fibrin Blood Clots
Blood Clot Destruction
• Plasminogen- released from fibrin clot• Turned into plasmin… • Fibrinolyis- plasmin dismantles blood clot• Takes hour to days
Blood Types
• A• B• AB• O
Rh Factor
Blood Compatibility
• AB- universal recipient• 0- universal donors• Type A- A-antigens, anti-B antibodies
Types of Transfusions
• Whole blood• Packed red blood cells• Platelets• Fresh frozen plasma• Clotting factors
Transfusion Reactions
• Facial flushing, hyperventilation, tachycardia, sense of dread
• Hives, chest pain, wheezing, fever, chills, cyanosis
Patient Assessment
• Petechiae (tiny red dots in skin)• Purpura (large purplish blothces)- high
bilirubin• Epistaxis• Enlarges spleen• Bleeding from gums• Arthralgia-pain and swelling in joints• Bleeding around IV site
Diseases of RBC
• Polycythemia- too many• Anemia- inadequate number of RBC or
inadequate hemoglobin
Anemia
• Symptom, not a disease• Hematocrit < 37 % in women < 40% in men• Pica- craving of unusual substances as ice or
clay
Sickle Cell Disease
• Inherited disorder of RBC production• Mom Xx Dad Xx• Babies XX Xx Xx xx• Xx – carriers of sickle cell trait• xx have disease
Polycytemia
• Hematocrit too high• > 50%• Rare disorder• 50 y/o +
WBC Diseases
• Leukopenia – too few (treatment is supportive)- prevent infection
• Leukocytosis – too many– Look for neutrophils with segmented nuclei
(bands)
Leukemia
• ALL, AML, CLL, CML, Hairy cell leukemia• High risk of infection
Lymphoma
• Cancers of the lymphatic system– Hodgkin’s lymphoma (better survival rate)– Nonhodgkin’s lymphoma
Platelet Diseases
• Thrombocytosis - Increase in number of platelets
• Thrombocytopenia- abnormal decrease in number of platelets
Hemophelia
• Disease in which one of the proteins necessary for blood clotting is missing or defective
• Hemophelia A- Deficiency in factor VIII (most common)
• Hemophelia B (Christmas Disease)- Deficiency if factor IX rarer and more severe
Hemophelia
• Sex- Linked• Normal Dad + Carrier Mom• XY + Xx• Children XX Xx (carrier) XY xY (hemophelia)
Von Willebrand’s Disease
• vWF component of factor VIII is deficient
Multiple Myeloma
• Cancerous disorder of plasma cells• Pain in ribs or back• Pathological fractures
DIC
• Disseminated Intravascular Coagulation• Caused by systemic activation of the
coagulation cascade• Widespread thrombosis• Bleeding due to decreased fibrinogen level,
consumption of coagulation factors, thrombocytopenia