問題一覧
1
Action: anatgonizes Vit K induces formation of PIVKAs;
Treatmen: Vit K administration
warfarin therapy
2
Enaces antithrombin III , inhuibits thrombin surgery during cardiac cathetherization and in several medical conditions;PROLONG APTT AND TCT
heparin therapy
3
Hypochromia grading
Thin rim of hemoglobin
4+
4
Area of pallor is three quarters
3+
5
Polychromasia grading
10%
3+
6
>11%
4+
7
Grading of erythrocyte morphology
Increased or few
1+
8
High reticukicyte count, excessive rbc loss includes
acute hemorrhage
9
Reflects body tissue iron stores
1st test to become abnormal when iron stores begin to decrease
serum ferritin
10
Not necessary for differential diagnosis
Tested when the disease is not obvious
serum iron
11
Measures the ability of transferrin to bind iron
Indirect measures of transferrin
TIBC
12
Increases when Fe is deficient
Protoporphyrin is the substance of to which Fe beinds to form heme
free eryhtrocyte protoporphyrin
13
Normocytic,normochromic, INCREASED ESR, INCREASED OR NORMAL FERRITIN LEVELS, DECREASED TIBC, SERUM IRON
anemia of chronic disease
14
Decreased serum iron, serum ferritin, and reticulocyte count
Increased RDW, TIBC
Iron deficiency anemia
15
Caused by blocks in the protoporphyrin pathways resulting to ineffective hemoglobin synthesis and iron overload
sideroblastic anemia
16
Microcytic, hypochromicRBCs and target cells, quantitative reduction of in globin chain
thalassemia
17
Marked decrease rate of synthesis or absence of both beta chains resulting an excess of alpha chains; NO HbA produced;compensated with up to 90% Hb F
major/homozygous (Cooley anemia)
18
One beta chain is normal; Hb A is slightly decreesed buf HbA2 is slightly increased to compensate
minor heterozygous
19
An alpha-thalassemia, all four alpha chains are deleteed; no normal Hb is produced:: aka hydrops fetalis
major alpha thalassemia
immuno 1
immuno 1
ユーザ名非公開 · 100問 · 7ヶ月前immuno 1
immuno 1
100問 • 7ヶ月前ユーザ名非公開
immuno 2
immuno 2
ユーザ名非公開 · 100問 · 7ヶ月前immuno 2
immuno 2
100問 • 7ヶ月前ユーザ名非公開
immuno 3
immuno 3
ユーザ名非公開 · 100問 · 7ヶ月前immuno 3
immuno 3
100問 • 7ヶ月前ユーザ名非公開
sero1
sero1
ユーザ名非公開 · 100問 · 7ヶ月前sero1
sero1
100問 • 7ヶ月前ユーザ名非公開
sero2
sero2
ユーザ名非公開 · 44問 · 7ヶ月前sero2
sero2
44問 • 7ヶ月前ユーザ名非公開
問題一覧
1
Action: anatgonizes Vit K induces formation of PIVKAs;
Treatmen: Vit K administration
warfarin therapy
2
Enaces antithrombin III , inhuibits thrombin surgery during cardiac cathetherization and in several medical conditions;PROLONG APTT AND TCT
heparin therapy
3
Hypochromia grading
Thin rim of hemoglobin
4+
4
Area of pallor is three quarters
3+
5
Polychromasia grading
10%
3+
6
>11%
4+
7
Grading of erythrocyte morphology
Increased or few
1+
8
High reticukicyte count, excessive rbc loss includes
acute hemorrhage
9
Reflects body tissue iron stores
1st test to become abnormal when iron stores begin to decrease
serum ferritin
10
Not necessary for differential diagnosis
Tested when the disease is not obvious
serum iron
11
Measures the ability of transferrin to bind iron
Indirect measures of transferrin
TIBC
12
Increases when Fe is deficient
Protoporphyrin is the substance of to which Fe beinds to form heme
free eryhtrocyte protoporphyrin
13
Normocytic,normochromic, INCREASED ESR, INCREASED OR NORMAL FERRITIN LEVELS, DECREASED TIBC, SERUM IRON
anemia of chronic disease
14
Decreased serum iron, serum ferritin, and reticulocyte count
Increased RDW, TIBC
Iron deficiency anemia
15
Caused by blocks in the protoporphyrin pathways resulting to ineffective hemoglobin synthesis and iron overload
sideroblastic anemia
16
Microcytic, hypochromicRBCs and target cells, quantitative reduction of in globin chain
thalassemia
17
Marked decrease rate of synthesis or absence of both beta chains resulting an excess of alpha chains; NO HbA produced;compensated with up to 90% Hb F
major/homozygous (Cooley anemia)
18
One beta chain is normal; Hb A is slightly decreesed buf HbA2 is slightly increased to compensate
minor heterozygous
19
An alpha-thalassemia, all four alpha chains are deleteed; no normal Hb is produced:: aka hydrops fetalis
major alpha thalassemia