Hemotalogy Blood Cell Alterations

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Last updated 7:03 PM on 3/28/26
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32 Terms

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What is the most common RBC disorder?

Anemia

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Anemia

 A deficiency in Number of erythrocytes (RBC’s)

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What are the causes of Anemia?

â—¦Blood loss because of injury or chronic bleeding in GI system

◦Decrease production of RBC’s in bone marrow

â—¦Not enough nutrients for production

â—¦Decrease in erythropoetin (needed to stimulate RBC production)

â—¦Hereditary chromosome abnormalities

◦Destruction of RBC’s (Hemolytic anemia)

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Signs and Symptoms of Anemia

â—¦Shortness of breath

â—¦Weakness, fatigue

â—¦Increased HR and RR

â—¦Pale skin, gums, and nail beds

â—¦Dizziness and confusion

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Normocytic Anemia

Normal size red blood cells

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Macrocytic Anemia

Large red blood cells

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Microcytic Anemia

Small red blood cells

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Anemia in Chronic Kidney Disease

When body low on RBC from normal RBC death, kidneys produce & release hormone erythropoietin (EPO). EPO stimulates the bone marrow to produce more RBC to replenish body.

Kidney failure = decreased EPO=decreased RBC production= anemia

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Normocytic Morphology Anemia

 Anemia from loss of blood or hemolysis(break up)of RBC’s

◦Acute – hemorrhage from traumatic injury, surgery, bleeding (burst) aneurysm

Hemolysis of RBC’s from blood transfusion reaction, reaction to a toxin or defect in RBC membrane

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 Iron Deficiency Anemia

 Most common anemia.

 Not enough iron for the body to make the correct amount

 of hemoglobin, therefore not enough RBC’s

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What causes Iron Deficiency Anemia?

â—¦Insufficient iron in diet

â—¦Loss of iron by chronic blood loss (usually ulcer or intestinal bleed)

â—¦Malabsorption

â—¦Stomach/colon cancer, bariatric surgery

â—¦Decreased absorption b/c insufficient absorption of stomach/colon

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Early Clinical Manifestations of Iron Deficiency Anemia

Fatigue

Weakness

Shortness of breath

Pale gums palms and conjunctivae

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Later (severe) Clinical Manifestations of Iron Deficiency Anemia

Spoon-shaped fingernails (koilonychia)

Scales and fissures in mouth (cheilosis)

Ulcerations of mouth and tongue

Headache

Cognitive impairment

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What are the most coomon Macrocytic Anemias?

B12 (cobalamin) Deficiency

Folic Acid Deficiency

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B12 (cobalamin) Deficiency

1.Not enough B12 for the body to make the correct amount & correct shape of RBC’s. Abnormal RBC’s die prematurely

â—¦Usually called Pernicious anemia

â—¦Disease autoimmune gastritis causes very low intrinsic factor (IF) secretion

of gastric membranes. Intrinsic factor needed for absorption of B12 .  

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Folic Acid Deficiency

â—¦Poor nutrition- lack of green, leafy veggies

â—¦some meds decrease absorption (methotrexate, anti-seizure)

â—¦Alcohol abuse

â—¦Hemodialysis patients

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Sickle Cell Anemia

 Caused by abnormal form of hemoglobin in the erythrocyte, hemoglobin S (HbS)

[Normal -hemoglobin A (HbA)]

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Aplastic Anemia

◦Pancytopenia (Decrease of all blood cell types, RBC’s, WBC’s, and platelets)

â—¦Bone marrow is suppressed fails to produce mature cells

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What are some causes of Aplastic Anemia?

 Most common cause: immune system attacking the stem cells the bone marrow

 

 Other possible causes:

 Some medications

Radiation and chemotherapy treatments

Viral infection

Exposure to toxic chemicals 

Inherited genes

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Polycythemia Vera

 Increased numbers of all blood cells, especially RBCs

â—¦Slowly growing blood cancer

◦Overproduction (proliferation) of RBC’s, hyperplasia of the bone marrow

◦Blood becomes very “thick”

Caused from chromosomal mutation

Usually >60 years of age when diagnosed

Usually in males

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Clinical Manifestations of Polycythemia Vera

Hypertension

Headache

Dizziness

Tinnitus

Heart failure

Thrombophlebitis

Shortness of breath

Enlarged spleen and liver

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Lymphomas

WBC disorder;  Neoplasms (tumors) developing from the proliferation of malignant lymphocytes in the lymph system

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What are the two major types of Lymphomas?

â—¦Hodgkin Lymphoma

â—¦Non-Hodgkin Lymphoma

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Non-Hodgkin Lymphoma

â—¦Malignant lymphocytes are B cells (not Reed-Sternberg) and T cells

â—¦Usually seen in males over the age of 55

Symptoms:

â—¦Can begin in lymph nodes anywhere in the body

â—¦Night sweats

â—¦Fever

â—¦Unexplained weight loss

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Hodgkin Lymphoma

â—¦Associated with malignant lymphocyte called Reed-Sternberg B cells

â—¦Usually seen in males less than 40 years

Symptoms:

â—¦Begins with enlarged lymph nodes of neck that do not diminish

â—¦Night sweats

â—¦Fever

â—¦Unexplained weight loss

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Multiple Myeloma

Cancer of the plasma cells (type of B cell)of the bone marrow

  • Tumors form in the bone marrow, cause “punched out” areas called lytic lesions.

  • Breakdown of bone releases calcium into the blood.

  • Many tumor cells means overcrowding of normal cells, fewer RBCs, WBCs, and platelets are produced

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Clinical Manifestations of Multiple Myeloma

Bone pain

Fractures

Fatigue

High calcium level/mental confusion                                                                                              

Depressed immune system

Frequent infections

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Thromnocytopenia

Decreased production in bone marrow or body destroying platelets

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Clincial Manifestations of Thrombocytopenia

â—¦Bruising under skin (purpura)

â—¦Excessive Nosebleeds (epistaxis)

â—¦Gum bleeds

â—¦Blood in vomit or stool

â—¦Petechiae- tiny purple, red, or brown spots on the skin

◦Intracranial bleeding                                         

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What causes of Thrombocytopenia?

â—¦Chemotherapy drugs and radiation therapy

◦    Aplastic anemia

◦    Leukemia and other cancers

◦    Viral infections, such as hepatitis C or HIV

◦    Heavy alcohol consumption

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Immune Thrombocytopenia Purpura

 Also called idiopathic thrombocytopenia purpura

  • Immune system is stimulated to attack and destroy body's own platelets

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What stimulates Immune Thrombocytopenia Purpura to happen?

â—¦Bacteria in the blood

â—¦Pregnancy

â—¦Immune disorders (rheumatoid arthritis and lupus)

â—¦Medications (heparin, quinine, sulfa-containing antibiotics and anticonvulsants)

◦Sometimes the cause is not known                 

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