Session 13 Flashcards

1
Q

what are the three main functions of the lymphatic system?

A
  1. removal of excess tissue fluid 2. absorption and transport of fat to the circulatory system and 3. production of immune cells
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2
Q

how does lymph originate?

A

as blood plasma from the capillaries that becomes the fluid that fills the spaces between the cells and tissues

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3
Q

what re the 4 major parts of the lymphatic system?

A

thymus, spleen, lymph nodes and bone marrow

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4
Q

what are the two distinct type of multipotential stem cells?

A
  1. lymphopoietic (lymphoid) stem cells which migrate to lymphoid organs for immune system and 2. multipotential hemopoietic (myeloid) stem cells which remain in the marrow
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5
Q

what is known as a reduction in circulating erythrocyte mass?

A

anemia

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6
Q

a demonstrated reduction in HCT, hemoglobin or RBC count is diagnostic for what?

A

anemia

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7
Q

what is the ultimate end game for anemia?

A

leads to decreased oxygen delivery which leads to tissue hypoxia

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8
Q

how is RBC size reflected?

A

in mean corpuscular volume (MCV)

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9
Q

what is the difference btwn normoochromic and hypochromic anemia?

A

normo has normal content of hemoglobin while hypo has reduced content hemoglobin

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10
Q

what is the term for abnormally shaped RBCs? what is the combination of both irregular size and shape? what is defined as irregular size?

A

poikilocytosis; anisopoikilocytosis; anisocytosis

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11
Q

what is the major disturbance with megaloblastic anemia?

A

disturbance of dna synthesis

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12
Q

what is the major disturbance of iron deficiency?

A

disturbance in hemoglobin synthesis; lack of iron

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13
Q

what is the major disturbance for hereditary spherocytosis anemia?

A

membrane defect

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14
Q

what is the major disturbance in hereditary elliptocytosis ?

A

membrane defect

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15
Q

what is the major disturbance in hemoglobin c disease anemia?

A

abnormal globin chain

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16
Q

what is the major disturbance in acanthocytosis?

A

membrane lipid defect

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17
Q

i say abetalipoproteinemia, you say?

A

acanthocytosis

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18
Q

mechanical damage to erythrocytes caused by such things as DIC, TTP, and heart valve prosthesis sequela will all lead to what kind of RBCs?

A

schistocytes

19
Q

what is the major disturbance in sickle cell anemia?

A

abnormal globin chain which produces sickle cells

20
Q

what is the major disturbance that is the cause of thalassemia?

A

disturbance in hemoglobin synthesis

21
Q

i say oval macrocytes with hypersegmented neutrophils, you say?

A

megaloblastic anemia

22
Q

what is the shape to look for with megaloblastic anemia?

A

teardrop poikilocytosis

23
Q

what is the type or RBCs you are looking for in iron deficiency anemia? (2)

A

hypochromic and microcytic

24
Q

what are the cells of thalassemia described as? (3)

A

hypochromic, microcytic cells with basophilic stippling

25
Q

which pathophysiologic classification of anemia is associated with increased numbers of circulating reticulocytes (reticulocytosis)?

A

anemias associated with increased destruction or loss of RBCs

26
Q

what is the most common anemia worldwide?

A

iron deficiency

27
Q

T or F: iron requirements increases during pregnancy?

A

TRUE

28
Q

iron deficiency in adults is most commonly a result of what?

A

blood loss (chronic); in young women (reproductive years) it is most commonly assoc with blood loss rom menstruation

29
Q

in post menopausal women, unexplained iron deficiency should prompt a study of what type?

A

GI tract tumor or vascular lesions

30
Q

what happens to the bone marrow in iron deficiency anemia?

A

bone marrow displays erythroid hyperplasia and decreased or absent stored iron

31
Q

what happens to the levels of serum iron, ferritin levels, and total iron biding capacity? and what about the serum transferrin

A

decreased, decreased and increased (due to increased serum transferrin)

32
Q

what happens to the saturation of transferrin in iron deficiency anemia?

A

it is lowered

33
Q

chronic anemia does what to the body’s iron store?

A

they are normal or even slightly increased

34
Q

hypocelllular bone marrow and pancytopenia is indicative of what?

A

aplastic anemia

35
Q

which anemia is really the result of injury to bone marrow stem cells?

A

aplastic anemia

36
Q

what are the two types of aplastic anemia?

A

does dependent )predictable) and dose independent (idiopathic)

37
Q

the bone marrow in aplastic anemia shows increased or decreased cellularity? what happens to the corresponding fat levels?

A

reduced cellularity with increased in fat

38
Q

anemia of chronic renal insufficiency is reflected by a decreased producing of what?

A

EPO (erythorpoietin)

39
Q

T or F: the anemia of chronic renal disease is hyperchromic and normocytic

A

FALSE: normocytic and normochromic

40
Q

in some cases of anemia due to chronic renal disease you will find RBC’s with scalloped cell membranes - what are these RBCs called?

A

Burr cells

41
Q

how doe lead poising result in anemia?

A

interferes with the enzymes involved in heme synthesis

42
Q

what is the difference between ineffective hematopoiesis and stem cell or precursor cell disorders?

A

the bone marrow erythrocyte precursor pool is expanded with ineffective hematopoiesis

43
Q

true or false: megaloblastic anemia results in the formation of large nucleated erythrocyte precursors (megaloblasts), most of which do not mature enough to be released into the blood but rather undergo intramedullary destruction.

A

true