Diseases of the blood, disease of the heart and blood vessels Flashcards
Produced in red bone marrow, some in lymphoid tissue.
- 5,000-9,000 cells/microliter of blood
- Function- inflammation, immunity
Leucocytes (White blood cells, WBC)
Produced in red bone marrow.
- 4,000,000- 5,000,000 cells/ microliter of blood
- Function- carry oxygen to cells and tissues, and carbon dioxide out of tissues.
Erythrocytes (Red blood cells, RBC)
Produced in red bone marrow
- 150,000-450,000 cells/microliter of blood
- Function- blood clotting
Thrombocytes (platelets)
Increase in the number of WBC in blood.
- Usually occurs to fight infection.
- May be physiological (protective, transient, more common) or pathological
- more than 9,000 cells/ microliter, up to 50,000
- The more severe the infection, the higher the number.
- 50,000 - 800,000 cells/microliter > indicate cancer of WBC producing tissue (leukemia)
Leucocytosis (Leukocytosis)
Abnormal reduction in the number of WBC in blood.
- Usually due to damage to bone marrow or lymphatic tissue
- results in anemia, infections, bleeding, bruising.
Leucopenia (leukopenia)
- Radiation
- Chemical poisons
- Some infections
Etiology of Leucopenia
Leucocytosis
Leucopenia
Reactive changes
A decrease in the number of erythrocytes, hemoglobin, or both resulting in decreased ability to carry oxygen to the body tissues.
Anemia
Chronic, hematologic disease that is a result of a love level of RBC or hemoglobin.
Primary anemia
Concerned with blood or blood-forming structures.
Hematologic
Develops as a complication of another disease, nonhematologic disease.
- persisting longer than 2-6 months
- May provide a diagnostic clue to a chronic disease, e.g., chronic osteomyelitis
Secondary anemia
- Increased destruction anemia
- Decreased production anemia
Two types of anemia
RBCs are being destroyed.
Increased destruction anemia
Producing less RBCs than normal.
Decreased production anemia
- Hemorrhage
- Injury or trauma
- Genetic
- Infections
Etiology of increased destruction anemia
Sickle cell anemia (primary)
Erythroblastosis fetalis (primary)
Hypersplenism (secondary)
Types of increased destruction anemia
Genetic mutation resulting in hemoglobin S
- cells of weird shape, form clots > spleen traps and destroys these cells.
- Results in tachycardia, fatigue, dyspnea
Sickle cell anemia (primary)
Hemolytic disease of the newborn. The mother and baby have different Rh blood types.
-baby’s RBCs are immature and larger than normal (with nucleus) > may form blood clots > trapped in spleen and destroyed.
Erythroblastosis fetalis (primary)
Overactive spleen due to mononucleosis or liver cancer.
- may cause splenomegaly (spleen enlargement).
Hypersplenism (secondary)
Underactive bone marrow due to:
- radiation
- chemical poisons
- infection
- metabolic disorders
- leukemia or bone cancer (osteosarcoma)
Etiology of decreased production anemia
Aplastic anemia
Pernicious anemia
Megaloblastic anemia
Types of decreased production anemia
Damage to bone marrow of unknown origin (idiopathic).
-bone marrow does not produce enough, or any, blood cells, especially RBC.
Aplastic anemia
Vitamin B12 deficiency
- due to lack of intrinsic factor produced in the stomach
- common in women following childbirth or malnutrition disorder.
Pernicious anemia
Deficiency of B12 and folic acid.
- megablasts
- associated with pernicious anemia.
Megaloblastic anemia
Large RBCs
Megablasts
Associated with formation of blood and blood components.
Hematopoietic (hemopoietic) disorders
“White blood”, cancer of WBC producing structures/organs (bone marrow, lymphatic tissue, or spleen).
- results in overproduction of immature WBC
- WBC count elevated 10-100 times.
Leukemia
Acute
Chronic
Types of leukemia
More common in children
- Acute myelocytic leukemia
- Acute lymphocytic leukemia (ALL)
- in children (age 3-6)
- cause severe anemia, pneumonia, infections
Acute Leukemia
More common in adults.
- Chronic myeloid leukemia
- Chronic lymphocytic leukemia
Chronic Leukemia
primary- Bone marrow makes too many RBCs (erythrocytosis) causing thickening of blood > slower blood flow
-Greater risk of forming blood clots
Polycythemia Vera
- headache, dizziness, itchiness and redness of skin
- fatigue, shortness of breath
- numbness, tingling, burning or weakness in hands, feet, arms or legs
- enlarged spleen
Symptoms of polycythemia vera
Increase in the number of RBC in blood (increased hematocrit)
-rare
Erythrocytosis
- Hereditary condition
- Excess blood in transfusion
- Underactive spleen (does not remove and destroy old RBC)
- polycythemia vera
Etiology of erythrocytosis
Increased blood volume.
Plethroa
- Plethroa
- Higher risk or forming blood clots/thrombi
- extra strain on heart > congestive heart failure > ischemia > cyanosis
- Enlarged spleen (splenomegaly), risk of rupture as it gets bigger.
May result from erythrocytosis
Decreased number of RBC in blood (decreased hematocrit), may result in anemia.
Erythrocytopenia
Leukemia
Polycythemia vera
Erythrocytosis
Erythrocytopenia
Type of hematopoietic disorders
Severe decrease in the number of platelets.
- less than 60,000 platelets/microliter of blood.
- Due to damaged bone marrow, e.g., radiation, chemicals, cancer (leukemia)
- Results in decreased ability to clot or coagulate blood.
- Bruise and bleed easily > results in hemorrhage, circulatory shock.
- Bruising > purple discoloration on the skin > immune thrombocytopenic purpura.
Thrombocytopenia
Blue color on lips and fingers due to lack of oxygen.
Cyanosis
- Immune system destroys its own platelets.
- Spontaneous bleeding in subcutaneous tissues > purple patches on the skin.
e.g., acute pediatric viral illness
Immune thrombocytopenic purpura