Alterations Of Hematologic Function Flashcards

1
Q

What are the four causes of anemia?

A

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2
Q

Differentiate hemoconcentratian from hemodilution

A

These terms describe the state of the total mass of circulating red blood cells. it can be hemoconcentration with decreased plasma vol or hemodilution with increased plasma vol.

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3
Q

Name the overall symptoms of anemia and why do they vary between people?

A

Increased respirations, increased fatigue, dizziness, weakness, pallor skin, lethargy, fainting.
Symptoms vary because the clinical manifestations depend on the bodies ability to compensate for the reduced 02 carrying capacity

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4
Q

What is the initial compensation for anemia within the body?

A

The movement of interstialfluid into the blood to increase plasma vol.

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5
Q

What type of anemia causes the skin to appear yellow and why?

A

Pernicious anemia because of the combination of pallor and jaundice

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6
Q

What is the difference between anemia and polycythemia Vera?

A

Anemia is not enough RBC’S and polycythemia is the creation of too many RBC’S (cancer)

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7
Q

What type of anemia affects nerve function and what are the symptoms?

A

The kind of anemia that occurs because of a lack of vitamin b12,

The symptoms are: numbness, gait disturbances, extreme weakness, spasticity, and reflex abnormalities

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8
Q

What are the compensatory mechanisms that occur with hemorrhage?

A

Peripheral blood vessel constriction, this is needed so that the blood is diverted to the essential organs.

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9
Q

What are the anemias of diminished erythopoiesis caused by?

A

The ineffective erythrocyte DNA synthesis caused by a lack of B12 or folate

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10
Q

Explain what is occurring in macrocytic (megaloblastic) anemia

A

Unusually large stem cells in the marrow mature into red blood cells that are also unusually large in size, thickness, and volume. These defective red blood cells die prematurely causing a decrease in red blood cells circulating in the blood causing anemia. The defective DNA synthesis causes red blood cells and development to occur and unequal rates causing blockage or a delay of the production of red blood cells. This causes an overproduction of hemoglobin during cell division which causes large red blood cells to be produced with disproportionately small nucleus‘.

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11
Q

What occurs with intrinsic factor (IF) in pernicious anemia?

A

The deficiency of IF is usually associated with end of stage type A chronic atrophic gastritis. The autoimmune gastritis impedes the production of IF, which is needed for the uptake of vitamin B 12 from the gut. B12 and IF is needed for nuclear maturation and DNA synthesis of red blood cells. When this is impeded this leads to anemia.

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12
Q

What other auto immune diseases are associated with pernicious anemia?

A

Endocrine diseases like type one diabetes, hypo parathyroidism, Addison’s disease, and Graves’ disease.

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13
Q

What are the symptoms of pernicious anemia – both early and when the hemoglobin is extremely low?

A

The early symptoms include infection, mood swings, G.I., cardiac, and kidney ailments.

When hemoglobin levels are between 7-8G/DL the symptoms include weakness, fatigue, paresthesias of feet and fingers, difficulty walking, loss of appetite, abdominal pain, weight loss, yellow skin, right sided heart failure, and sore tongue.

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14
Q

Who is most likely to suffer from folate deficiency anemia?

A

People who are alcoholics and people with chronic malnourishment

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15
Q

Who is most at risk for iron deficiency anemia?

A

Toddlers, adolescents, childbearing women, those living in poverty, infants consuming cows milk, older people with restricted diet, and teenagers eating junk food.

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16
Q

What are the causes of IDA (Iron deficiency anemia)?

A

dietary deficiency, impaired absorption, increase requirement, chronic blood loss, impaired absorption, and chronic diarrhea.

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17
Q

What are the stages of IDA and what is happening each stage?

A

In stage one there is decreased bone marrow iron stores but the hemoglobin and serum iron remain normal. And stage to iron transport to the bone marrow diminishes which makes iron deficient erythropoiesis. And stage three the iron deficient red blood cells replace the normal age red blood cells from circulation. The clinical manifestations appear in stage three when there is a depletion of iron stores and diminished hemoglobin production.

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18
Q

What is the symptoms of IDA when the hemoglobin levels are extremely low?

A

Koilonychia (spoon shaped fingernails), cheilosis, stomatitis, painful ulcerations of bucal Mukosa and tongue, dysphasia, and burning mouth syndrome.

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19
Q

How do we know the treatment for IDA is working?

A

A measurement of serum ferritin levels is a precise way of measuring improvement. Hematocrit levels should increase 1 to 2 months of therapy. Decrease in fatigue and lethargy should be seen within the first month.

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20
Q

What is anemia of chronic disease (ACD) and what kind of diseases is it see in?

A

Anemia of chronic disease is a mild to moderate type of anemia that results from the decreased red blood cell production and impaired iron utilization and individuals with chronic conditions of chronic systemic disease or inflammation.

It is often seen in infections, cancers, and auto immune diseases

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21
Q

What is happening in the body that leads to ACD?

A

The chronic information reduces the body’s ability to absorb and use iron for our red blood cell production. The inflammation increases the production of hepcidin. Hepcidin inhibit iron absorption in the duodenum and the release of iron from macrophages.

When there’s not enough iron to be absorbed, there is not enough iron for the production of red blood cells.

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22
Q

What is the most significant finding of ACD that makes it different from IDA?

A

There is a high total body iron storage, but in an adequate iron release from bone marrow for erythropoiesis.

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23
Q

What does a return to normal levels in ACD make the patient at risk for?

A

Hypertension, stroke, and death.

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24
Q

What is aplastic anemia?

A

It is a hematopoietic failure or bone marrow aplasia with a reduction in the effective production of mature cells by bone marrow causing pancytopenia. Pancytopenia means all blood cell lines are decreased. This means there is a decrease of red blood cells, white blood cells, and platelets.

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25
Q

What are the normal red blood cell levels

A

In men it is 4.7 to 6.1 cells/mcL

In woman it is 4.2 to 5.4 cells/mcL

26
Q

What are the normal levels of white blood cells

A

4,000 to 11,000

27
Q

Are the normal levels of platelets

A

140,000 to 450,000

28
Q

Are the clinical manifestations of aplastic anemia?

A

Cardiovascular and respiratory manifestations such as thrombocytopenia, hemorrhage into the tissues, leukopenia, and infection

29
Q

How is aplastic anemia treated?

A

There must be treatment of an underlying disorder for prevention. Blood transfusions, marrow transplant, and pharmacological stimulation of bone marrow function.

30
Q

What is erythropoietin

A

A hormone that stimulates red blood cell production

31
Q

Define polycythemia and differentiate between relative polycythemia and secondary polycythemia

A

Polylenthemmia is excessive red blood cell production.

Relative polycythemia is Hemoconcentration caused by dehydration, diarrhea, excessive vomiting, or increased use of diuretics.

Secondary polycythemia is a physiological response to erythropoietin secretion caused by hypoxia. The hypoxia can be due to high altitudes, smoking, COPD, and/or heart failure.

32
Q

What is polycythemia vera?

A

It is a slowly growing blood cancer where the bone marrow makes too many red blood cells.

33
Q

What is the cause of PV?

A

The abnormal regulation of hemopoietic stem cells and a mutation in the Janus kinase 2 gene (JAK2 gene).

34
Q

What are the clinical manifestations of PV?

A

Tissue injury (ischemia), death via infarction, plethora (ruby red color), engorgement of retinal and cerebral veins, headache, drowsiness, delirium, mania, depression, chorea, visual disturbances, and enlarged spleen causing abdominal pain and discomfort.

35
Q

How is PV treated

A

Reducing red blood cell proliferation and blood volume, controlling symptoms, and preventing clogging/clotting of blood vessels.

36
Q

Compare leukocytosis and leukopenia and their causes

A

Leukocytosis is an increase in white blood cell count for the protection of the body. This is normal and the causes are infection or illness.

Leukopenia is a decreased white blood cell count, less than 4000 cells. This is abnormal and it’s caused by radiation, auto immune disease, immune deficiencies, some drugs, and glucocorticoids and chemotherapeutic agents.

37
Q

What are granulocytes and what is granulocytosis?

A

Granulocytes include neutrophils, eosinophils, and basophils.
Granulocytosis is an increase in granulocytes, it begins when stored blood cells are released.

38
Q

At what level is severe neutropenia diagnosed and what happens if the condition remains and untreated

A

Neutropenia is the reduction and circulating neutrophils. It begins to present clinical manifestations at less than 2000. If it remains untreated it can result in sepsis and then death.

39
Q

What can cause eosinophilia?

A

Eosinophilia can be caused by hypersensitivity reactions and mast cells release of Interluken – 5 (Ik-5)

40
Q

What is lympocytosis and when is it seen?

A

Lymphocytosis is an increase in the number or proportions of lymphocytes in the blood.
It is seen in acute viral infections usually caused by the Epstein-Barr virus.

41
Q

What is AIDS- related lymphocytopenia caused by?

A

HIV because it destroys T-helper lymphocytes.

42
Q

What is infectious mononucleosis(IM)?

A

It is a benign, acute, self-limiting, lymphoproliferative clinical syndrome characterized by acute viral infection of B lymphocytes

It is caused by (EBV) Epstein-Barr virus

43
Q

What are the symptoms of IM?

A

Early flu like symptoms followed by fever, sore throat, cervical lymph node enlargement, fatigue, and pharyngitis that is painful and has whitish or grayish green thick exudate.

44
Q

Why is aspirin avoided in children with IM?

A

Aspirin is avoided because of it’s association with Reye syndrome.

*Reye syndrome is a rare but serious condition that causes confusion, swelling in the brain, and liver damage.

45
Q

What is the common pathology occurring with leukemia?

A

The hemopoetic cells overproduce unmature blast cells that have mutated jeans that do not allow for matturation and remove the control of a replication.

46
Q

Compare acute and chronic leukemia

A

Acute leukemia is characterized by undefiateiated cells (blast cells). This is abrupt and rapid. Without treatment the disease progression can result in a short survival time.

Chronic leukemia is characterized by predominantly differentiated cells that do not function properly.

47
Q

What is the most common childhood leukemia?

A

Acute lymphocytic leukemia (ALL)

48
Q

What is the most common adult leukemia?

A

Acute myelogenous leukemia (AML) and chronic lymphocytic leukemia (CLL)

49
Q

What are the clinical manifestations of acute leukemia

A

Fatigue, bleeding in the skin, gums, mucous membranes, and G.I. tract. Fever, petechiae, ecchymosis, discoloration, hematuria, and heavy menstrual bleeding.

50
Q

Define lymphadenopathy

A

it means enlarged lymph nodes

51
Q

Differentiate between localized and generalized lymphadenopathy

A

Localized lymphadenopathy indicates drainage of an area associated with inflammation or infection.

Generalized lymphadenopathy occurs less often and is present in the presence of infection, auto immune disease, or disseminated malignancy.

52
Q

What is present in Hodgkins lymphoma (HL) that is different than non-Hodgkins lymphoma?

A

In Hodgkins lymphoma there is a presence of RS cells (reed Sternberg cells).

53
Q

What are the systemic symptoms of HL?

A

Cytokines and growth factors are released by malignant cells. This result in infiltration and proliferation of inflammatory cells causing a large lymph node on the neck to appear.

54
Q

What is multiple myeloma (MM) and how does it affect production of blood cells?

A

Multiple myeloma is a colonial plasma cell cancer characterized by the slow proliferation of tumor cells in the bone marrow.

Myeloma cells reside in the bone marrow and as the number of myeloma cells increase the number of red blood cells, white blood cells, and platelets decrease.

The myeloma cells take away resources, space, and the necessary things that are required for red blood cells, white blood cells, platelets to be produced

55
Q

What are the clinical manifestations that characterize MM?

A

Elevated calcium levels, renal failure, and bone lesions.

56
Q

Compare and contrast thrombocytopenia with thrombocytosis

A

 thrombocytopenia is a platelet count less than 150,000 platelets.

Thrombocytosis is a platelet count greater than 450,000 and is asymptomatic until the exceeds 1 million platelets

57
Q

What can cause thrombocytopenia?

A

A decrease platelet production or increased platelet consumption

58
Q

What typically causes 50% drop in platelet count?

A

Heprin induced thrombocytopenia

59
Q

Why does vitamin K deficiency predispose an individual to a coagulation disorder

A

Vitamin K is needed for the synthesis and regulation of prothrombin, the coagulation factors and the anticoagulant factors in the liver.

60
Q

What is DIC in what are the clinical manifestations?

A

DIC is means disseminated intravascular coagulation. It is widespread coagulation resulting in the formation of fibrin clots in medium and small vessels.

Clinical manifestations depend on the underlying disease processes. It can include bleeding or thrombosis, hemorrhaging. Indicators of multisymptom dysfunction include consciousness or behavior changes, confusion, seizure, hematuria, hypoxia, hypotension, chest pain and tachycardia.

61
Q

Compare and contrast a thrombus with an embolus

A

Both a thrombus and embolus are a clot. But a thrombus is attached to a vessel wall while an embolus is circulating and no longer attached.

62
Q

Is the treatment for iron overload?

A

Therapeutic phlebotomy to remove the excess iron