問題一覧
1
control of cellular function and transmission of genetic information
DNA
2
Acute Hyperemia
Blushing
3
/Joseph Diamond
cell aplasia
4
Detectable of Hb synthesis
Basophilic normoblast
5
RBC characteristics Average lifespan:
120 days
6
Bizarre multinucleated erythroblasts,
Congenital dyserythropoietic anemia
7
Beginning of Hb formation
Pronormoblast
8
-the first stage in which the pink color associated with stained hemoglobin can be seen
Polychromatic normoblast
9
RBC characteristics Low RBC (only) with normal WBC and platelet
B ICE PAC Blackfan anemia/Congenital red Imperfecta/Chronic Cell aplasia/Joseph Diamond Erythroblastopenia/primary red Pure red cell anemia/Diamond Anemia/Erythrogenesis Cell aregenerative
10
blackfan anemia/
Congenital red
11
-Increase RBC mass/count
Polycythemia
12
AKA/Imperfecta
Chronic
13
Anaerobic ATP production
EMP
14
Affected by warfarin
Factor VII
15
Affected by superwarfarin
Factor VII
16
-parasite – causes Megaloblastic anemia, low Vit B12, Macrocytosis
D.latum
17
Hypersegmented neutrophil Hallmark of
Megaloblastic anemia
18
Migrate with Hemoglobin E
Hb C
19
The function of thromboplastin in the prothrombin test is to provide _____ to the assay
Phospholipoprotein
20
Polycythemia vera - ESR?
Increase
21
Production of glutathione that detoxifies peroxide
HMS
22
Lab findings in Megaloblastic anemia
Ovalocytes and Pancytopenia
23
DNA Replication:
: S phase
24
, increased unconjugated bilirubin, and ineffective
Congenital dyserythropoietic anemia
25
considered to be the “gold standard” of molecular methods
DNA sequencing
26
- Chloramphenicol is the drug most often implicated in
acquired aplastic anemia
27
RBC characteristics color
Pink
28
Aplastic Anemia - ESR?
decrease
29
-JAK 2 mutation
Polycythemia vera
30
/primary red
erythroblastopenia
31
RBC transfusion is primarily to:
Increase Oxygen carrying capacity
32
Unique to platelet
Open canalicular system
33
Splenectomy Increases? (4)
Increase platelet Increase WBC Increase cell inclusion Increase spherocytes
34
RBC characteristics thickness
140 um2
35
Immature RBC without nucleus
Reticulocytes
36
cytokines for stem cell mobilization
GCSF and GM-CSF
37
LOCATION OF TPO production
Liver
38
Last nucleated stage (RBC)
Orthochromic normoblast
39
-Hemoglobin appears for the first time
Polychromatic normoblast
40
Meiosis the cells produced contain ? chromosomes
23
41
Not detected by PT or PTT
Platelet factor Factor XIII
42
Unstable Hb 2 Zeta and 2 Beta
Portland 2
43
anemia/
Erythrogenesis
44
X-linked or sex-linked hemophilia -> Occurs in MALE X chromosome
Hemophilia A Hemophilia B
45
1. Numerous NRBCs 2. Pronounced POlychormasia 3. Decreased Hb and HCT
Red cell regeneration
46
Division of the cellular cytoplasm
Cytokinesis
47
cell aplasia/
Joseph Diamond
48
/Erythrogenesis
anemia
49
decrease Vit B12 or folate or both
Megaloblastic anemia
50
is used for Reticulocyte count
Miller disc
51
- is the drug most often implicated in acquired aplastic anemia
Chloramphenicol
52
Hallmark of Megaloblastic anemia
Hypersegmented neutrophil
53
RBC characteristics average volume
90fl
54
-Treatment with folic acid improves hematologic abnormalities but not neurologic problems
Megaloblastic anemia
55
use to amplifies low levels of specific DNA sequences
PCR
56
- Last stage capable of mitosis
Polychromatic normoblast
57
Affected by coumadin
Factor VII
58
Differentiate between Vit B12 deficiency and Folate deficiency
Normal in folate def High in Vit B12 def
59
deficiency ? -bite cell
G6PD deficiency
60
- – lack of castle intrinsic factor leading to LOW VIT B12 ABSORPTION
Pernicious anemia
61
erythroblastopenia/
primary red
62
-Pancytosis (accd to Harr, it should be panmyelosis)
Polycythemia vera
63
Stain for Reticulocytes
Methylene blue
64
Hypersegmented neutrophil (nucleus ?)
greater than 6 lobes
65
G6PD deficiency -Hemolysis by ? and ?
fava beans and primaquine
66
-Hemolysis by fava beans and primaquine
G6PD deficiency
67
RBC characteristics Pallor:
1/3 of the cell
68
-D.latum – causes (3)
Megaloblastic anemia, low Vit B12, Macrocytosis
69
AKA//Chronic
Imperfecta
70
Differential test between Vit B12 deficiency and Folate deficiency
Serum methylmalonic acid
71
Affected by brodifacoum
Factor VII
72
Stem cell CD marker
CD34
73
RBC characteristics um
6-8
74
the most frequently used site for bone marrow aspiration and biopsy
iliac crest
75
the cells produced contain 23 chromosomes
Meiosis
76
Lifespan of platelet is
8 to 12 days/ 9 to 10 days
77
MCV is SLIGHTLY HIGHER in ? or ?
Polychromasia or reticulocytosis
78
-Pernicious anemia – lack of ? factor leading to LOW VIT B12 ABSORPTION
castle intrinsic
79
-failure to produce RBC, WBC, and platelets (pancytopenia)
Aplastic Anemia
80
- bone marrow failure syndrome/empty and hypoplastic bone marrow
Aplastic Anemia
81
Miller disc is used for ?
Reticulocyte count
82
PASSWORD CESS Increase platelet Increase WBC Increase cell inclusion Increase spherocytes
Splenectomy
83
Liver ? production
TPO
84
Last coag in extrinsic and intrinsic pathway
factor 2
85
FFP and CP are NOT USED in ANY platelet disorder example is ______
ITP
86
LASER –
Light Amplified by Stimulated Emission of Radiation
87
Appropriate test for PNH
Sucrose hemolysis If may FLOW CYTOMETRY sa choices, then flow cytometry answer
88
: : S phase
DNA Replication
89
first hemoglobin-synthesizing cell (hubbard)
Pronormoblast
90
Unstable Hb Portland 2 CONTAINS?
2 Zeta and 2 Beta
91
-decrease ESR
aplastic anemia
92
Reduce ferric to ferrous
MRS (methemoglobin reductase shunt/pathway)
93
-Increase ESR
Polycythemia vera
94
Megaloblastic anemia -Treatment with ? improves hematologic abnormalities but not neurologic problems
folic acid
95
Factor Affected by coumarin
Factor VII
96
-lymphocyte production is less affected
Aplastic Anemia
97
Last coag factor in extrinsic and intrinsic pathway
Factor I
98
is SLIGHTLY HIGHER in Polychromasia or reticulocytosis
MCV
99
AKA/Congenital red
Blackfan anemia
100
first inherited hematologic disorder to be diagnosed using molecular biologic assay
Sickle cell anemia