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