B3-034 Introduction to RBC Disorders Flashcards

1
Q

primary growth factor involved in erythropoiesis

A

erythropoietin

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2
Q

erythroids have a _________ maturation time

A

7 days

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3
Q

during erythroid maturation, the nucleus becomes

A

smaller and darker until it is dissolved

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4
Q

during erythroid maturation, the cytoplasm becomes

A

more pink

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5
Q

round, biconcave disks with central pallor
anucleate
eosinophilic cytoplasm

A

erythrocytes

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6
Q

oxygen transport

A

erythrocytes

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7
Q

total number of erythrocytes

A

RBC

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8
Q

total amount of hemoglobin

A

Hgb

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9
Q

proportion of blood occupied by RBCs

A

Hct

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10
Q

mean RBC volume/size
-cytic

A

MCV

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11
Q

average amount of hemoglobin in each RBC

A

MCH

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12
Q

average amount of hemoglobin per RBC volume
-chromic

A

MCHC

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13
Q

variation in RBC size

A

RDW

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14
Q

variation in size

A

anisocytosis

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15
Q

variation in shape

A

poikilocytosis

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16
Q

variation in size and shape

A

anisopoikilocytosis

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17
Q

immature RBCs containing residual RNA

A

reticulocyte

**aka polychromatic erythrocyte

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18
Q

circulating time of reticulocytes [increase/decreases] in anemia

A

increases

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19
Q

reticulocytes survive for _______ before becoming mature RBC

A

1 day

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20
Q

correlate with bone marrow erythropoietic activity

A

reticulocytes

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21
Q

low count of reticulocytes indicates

A

decreased RBC production

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22
Q

high count of reticulocytes indicates

A

increased RBC production

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23
Q

normal range of reticulocytes

A

.5-1.5% of total RBCs

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24
Q

measurements of anemia

A

Hgb, Hct, RBC

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25
low total body red cell mass
anemia
26
clinical features of anemia
pallor of skin, nail beds, buccal mucosa fatigue, weakness, malaise dyspnea on exertion syncope, headaches, visual disturbances tachycardia angina cardiac failure
27
caused by inadequate or ineffective production
hypoproliferative anemia
28
causes of inadequate production in hypoproliferative anemia
bone marrow failure bone marrow infiltration/replacement nutritional deficiency anemia of chronic disease
29
causes of ineffective production in hypoproliferative anemia
myelodysplastic syndromes
30
caused by blood loss or sequestration
anemia of blood loss
31
sequestration causes
splenomegaly
32
anemia of blood loss can be
acute or chronic
33
sickle cell is [intrinsic/extrinsic] and [inherited/acquired]
intrinsic inherited
34
hemoglobinopathy
sickle cell
35
thalassemia is [intrinsic/extrinsic] and [inherited/acquired]
intrinsic inherited
36
membrane abnormality
hereditary spherocytosis
37
hereditary sphereocytosis is [intrinsic/extrinsic] and [inherited/acquired]
intrinsic inherited
38
RBC enzyme defects
G6PD deficiency
39
G6PD deficiency is [intrinsic/extrinsic] and [inherited/acquired]
intrinsic inherited
40
paroxysmal nocturnal hemoglobinuria is [intrinsic/extrinsic] and [inherited/acquired]
intrinsic acquired
41
people with proxysmal nocturnal hemoglobinuria are predisposed to
cancer
42
autoimmune hemolytic anemia is [intrinsic/extrinsic] and [inherited/acquired]
extrinsic aquired
43
traumatic hemolytic anemia is [intrinsic/extrinsic] and [inherited/acquired]
extrinsic acquired
44
infection related anemia is [intrinsic/extrinsic] and [inherited/acquired]
extrinsic aquired
45
malaria can cause
anemia due to infection
46
prosthetic cardiac valves can cause
anemia due to traumatic hemolysis
47
defect in RBC itself
intrinsic
48
defect/problem outside of RBC
extrinsic
49
RBC breakdown with massive release of free hemoglobin in circulation
intravascular **malaria, babesia, complement activation
50
RBC breakdown in the reticuloendothelial system cells with capture of hemoglobin
extravascular
51
in extravascular hemolysis haptoglobin is [increased/decreased]
decreased or normal
52
in intravascular hemolysis haptoglobin is [increased/decreased]
decreased
53
in extravascular hemolysis serum free hemoglobin is [absent/present]
absent
54
in intravascular hemolysis serum free hemoglobin is [absent/present]
present
55
in intravascular hemolysis urine hemoglobin is [absent/present]
present
56
in extravascular hemolysis urine hemoglobin is [absent/present]
absent
57
hemolytic anemia has the same general features of anemia, with _________ &__________
jaundice and gallstones maybe splenomegaly if extravascular
58
circulating iron available for use
serum iron
59
iron transport protein
transferrin
60
serum iron/TIBC
percent saturation
61
marker of stored iron
ferritin
62
differential for microcytic anemia
iron deficiency anemia of chronic disease thalassemia
63
serum iron is [increased or decreased] iron deficiency: anemia of chronic disease: thalassemia:
serum iron iron deficiency: decreased anemia of chronic disease: normal or decreased thalassemia: normal
64
transferrin/TIBC is [increased or decreased] iron deficiency: anemia of chronic disease: thalassemia:
transferrin/TIBC iron deficiency: increased anemia of chronic disease: normal thalassemia: normal
65
% saturation is [increased or decreased] iron deficiency: anemia of chronic disease: thalassemia:
% saturation iron deficiency: decreased anemia of chronic disease: normal/decreased thalassemia: normal
66
ferritin is [increased or decreased] iron deficiency: anemia of chronic disease: thalassemia:
ferritin iron deficiency: decreased anemia of chronic disease: normal/increased thalassemia: normal or increased
67
soluble transferrin receptor is [increased or decreased] iron deficiency: anemia of chronic disease: thalassemia:
soluble transferrin receptor iron deficiency: increased anemia of chronic disease: normal thalassemia: normal
68
differential for macrocytic anemia
megaloblastic anemia myelodysplasia drugs hypothyroidism
69
megaloblastic anemia can be caused by what vitamin deficiencies
vitamin B12 folate
70
differential for macrocytic anemia
megaloblastic anemia myelodysplastic syndromes hypothyroidism
71
differential for microcytic anemia
IDA ACD thalassemia
72
most common cause of iron deficiency in US
chronic blood loss | GI, GU, or GYN tract
73
chronic renal disease would cause which type of anemia?
ACD
74
deficiency of intrinsic factor causes
B12 deficiency, megaloblastic anemia
75
in thalassemia, serum ferritin and iron are
normal
76
increased LDH indicates
hemolytic anemia
77
in hemolytic anemia, serum free haptoglobin is
decreased
78
in hemolytic anemia, breakdown of hemoglobin leads to increased bilirubin. this causes
jaundice, gallstones
79
decreased serum iron decreased ferritin increased serum transferrin increased TIBC
IDA
80
low MCV low MCH low MCHC low Hgb low Hct low RBCs
IDA
81
increased RDW
IDA
82
normal bone marrow contains ...% of erythroid cells
15-30%
83
thalassemia has a ...... RDW
normal
84
iron therapy stimulates
erythropoeisis, increasing the reticulocyte count
85
helpful tests in establishing hemolysis as cause of anemia
LDH, haptoglobin, bilirubin