Session 13 Flashcards

(43 cards)

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?

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
which pathophysiologic classification of anemia is associated with increased numbers of circulating reticulocytes (reticulocytosis)?
anemias associated with increased destruction or loss of RBCs
26
what is the most common anemia worldwide?
iron deficiency
27
T or F: iron requirements increases during pregnancy?
TRUE
28
iron deficiency in adults is most commonly a result of what?
blood loss (chronic); in young women (reproductive years) it is most commonly assoc with blood loss rom menstruation
29
in post menopausal women, unexplained iron deficiency should prompt a study of what type?
GI tract tumor or vascular lesions
30
what happens to the bone marrow in iron deficiency anemia?
bone marrow displays erythroid hyperplasia and decreased or absent stored iron
31
what happens to the levels of serum iron, ferritin levels, and total iron biding capacity? and what about the serum transferrin
decreased, decreased and increased (due to increased serum transferrin)
32
what happens to the saturation of transferrin in iron deficiency anemia?
it is lowered
33
chronic anemia does what to the body's iron store?
they are normal or even slightly increased
34
hypocelllular bone marrow and pancytopenia is indicative of what?
aplastic anemia
35
which anemia is really the result of injury to bone marrow stem cells?
aplastic anemia
36
what are the two types of aplastic anemia?
does dependent )predictable) and dose independent (idiopathic)
37
the bone marrow in aplastic anemia shows increased or decreased cellularity? what happens to the corresponding fat levels?
reduced cellularity with increased in fat
38
anemia of chronic renal insufficiency is reflected by a decreased producing of what?
EPO (erythorpoietin)
39
T or F: the anemia of chronic renal disease is hyperchromic and normocytic
FALSE: normocytic and normochromic
40
in some cases of anemia due to chronic renal disease you will find RBC's with scalloped cell membranes - what are these RBCs called?
Burr cells
41
how doe lead poising result in anemia?
interferes with the enzymes involved in heme synthesis
42
what is the difference between ineffective hematopoiesis and stem cell or precursor cell disorders?
the bone marrow erythrocyte precursor pool is expanded with ineffective hematopoiesis
43
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.
true