

blood system
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University
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Lida Aliyeva
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0 Slides • 70 Questions
1
Multiple Choice
The "triggering" factor for the volum-reflex is
hypervolemia
hypovolemia
normovolemia
tachycardia
blood loss
2
Multiple Choice
Polycythemia is:
decrease in erythrocytes, platelets
an increase in leukocytes and platelets
decreasing all shaped elements
increase in erythrocytes, leukocytes
increasing all shaped elements
3
Multiple Choice
Pancytopenia is a sign:
inhibition of erythropoiesis
suppression of bone marrow function
hemolysis of blood corpuscles
lack of megakaryoblasts
dysfunction of hematopoiesis
4
Multiple Choice
What leukemia are belong with acute:
erythromyelosis
myeloma
Vakez disease
lymphodenosis
megakaryocytic
5
Multiple Choice
Describe the state of the erythrocyte lineage of the bone marrow in anemia with an HB content of 60 g / l and reticulocytes in the peripheral blood equal to 0.9%:
aplastic
hypoplastic
aregenerator
regenerative
hyporegenerative
6
Multiple Choice
Indicate signs of erythrocyte degeneration:
basophilic granularity, Jolly bodies, vacuolization
Klein-Humprecht's little body, Jolly's little body, anisocytosis
anisochromia, Jolly's little bodies, pycnosis
apoptosis, toxic granularity, poikolocytosis
poikilocytosis, Jolly bodies, basophilic granularity
7
Multiple Choice
Hemoglobin 64 g / l; erythrocytes 2.08x1012 / l; leukocytes 84x109 / l; Myeloblasts-95.5, promyelocytes-absent. Neutrophils: Myelocytes, Young, Stab-absent. Segmented-2.0. Eosinophils, Basophils ,. Monocytes are absent. Lymphocytes-2.5. Your hematological diagnosis:
iron deficiency anemia
acute myeloid leukemia
leukemoid reaction
chronic myeloid leukemia
leukocytosis neutrophilic
8
Multiple Choice
In a 15-year-old teenager, target erythrocytes were found in the blood. What hemoglobin increase is a diagnostic criterion for beta-thalassemia?
HbA2
HbA1
HbСО
HbS
HbM
9
Multiple Choice
Disease accompanied by relative lymphocytosis:
Infectious mononucleosis
croupous pneumonia
tuberculosis
appendicitis
aplastic anemia
10
Multiple Choice
After long-term administration of analgin, a 25-year-old woman developed ulcerative-necrotic lesions of the oral mucosa. What is most likely to be found in the patient's blood?
significant decrease in neutrophils, relative lymphocytosis
neutrophilia and relative lymphopenia
significant decrease in neutrophils and absolute lymphocytosis
leukopenia with absolute monocytosis
the appearance of blast cells
11
Multiple Choice
Examination of a 50-year-old man who had undergone gastric resection 5 years ago revealed erythropenia, large oval erythrocytes and hypersegmented neutrophils in the smear. Most likely the patient has anemia:
hemolytic
B-12-deficient
aplastic
microspherocytic
iron deficiency
12
Multiple Choice
Stage 1 of DIC syndrome is characterized by:
necrotic changes in target organs
consumption coagulopathy
activation of proteolysis
hypocoagulation
hypercoagulability and platelet aggregation
13
Multiple Choice
In iron deficiency anemia, erythrocytes are usually found in the blood:
core
large
hypochromi
with Jolly bodies
hyperchromic
14
Multiple Choice
Eosinophilia occurs when:
lymphocytic leukemia
iron deficiency anemia
Addison-Birmer anemia
allergies
hemophilia
15
Multiple Choice
For hemolytic anemias, the characteristic is ....
iron deficiency in the body
megaloblastic type of hematopoiesis
fatty degeneration of red bone marrow
shortening the life span of erythrocytes
increased osmotic resistance of erythrocytes
16
Multiple Choice
Leukopenia can lead to ... .
development of body sensitization
decrease in blood clotting
decrease in body resistance
development of leukemia
reticulocytosis
17
Multiple Choice
The development of leukemia is based on ...
uncontrolled proliferation of hematopoietic cells
decreased mitotic activity of cells
increased activity of antiblastoma resistance of the organism
increased ability of cells to differentiate and mature
decreased activity of protooncogenes and transforming oncogenes
18
Multiple Choice
The factors contributing to thrombus formation include ....
activation of the anticoagulant system
thrombocytopenia
increased blood flow velocity
decreased blood clotting ability
damage to the vascular wall
19
Multiple Choice
Chronic post-hemorrhagic anemia is hyporegenerative, because:
there is a loss of erythrocytes, little erythropoietins
lack of a specific factor of erythropoiesis (iron)
there is a loss of plasma proteins
the bone marrow produces red blood cells poorly
there is a decrease in the mass of circulating blood
20
Multiple Choice
What explains the hyperchromia in Addison-Birmer anemia:
very low red blood cell count
the presence of megaloblasts and megalocytes
high hemoglobin
large diameter of megalocytes
lack of vitamin B12
21
Multiple Choice
Tumor disease of the blood system with diffuse damage to the hematopoietic tissue is:
leukemia
hematosarcoma
leukemoid reaction
agranulocytosis
pernicious anemia
22
Multiple Choice
Neutrophilic leukocytosis with a nuclear shift of the leukocyte formula to the left is characteristic for:
tuberculosis
measles
myocardial infarction
infectious mononucleosis
hay fever
23
Multiple Choice
Your conclusion on the hemogram is: erythrocytes - 3.2x1012 / l, hemoglobin - 60g / l, color index - 0.6, reticulocytes - 1%, leukocytes - 4.5x109 / l, sideropenia. In a blood smear - microcytes, hypochromic erythrocytes, poikilocytes.
acute acquired hemolytic anemia
vitamin B12-folate deficiency anemia
iron deficiency anemia.
hypo-aplastic anemia
acute post-hemorrhagic anemia.
24
Multiple Choice
Your conclusion on the hemogram is: erythrocytes - 1.2x1012 / l, Hb - 60g / l, color index - 1.5, reticulocytes - 0.3%, leukocytes - 3.5x109 / l, platelets - 180x109 / l. In a smear - anisocytosis and poikilocytosis of erythrocytes, megalocytes, megaloblasts.
vitamin B12-folate deficiency anemia.
hypo-, aplastic anemia.
acute acquired hemolytic anemia.
Iron-deficiency anemia.
acute post-hemorrhagic anemia.
25
Multiple Choice
Degenerative forms of leukocytes:
vacuolization, fragmentation, anisochromia, myelocytes
karyorrhexis, basophilic granularity, fragmentation
hypochromia, toxic granularity, Jolly's little bodies
anisochromia, pycnosis, poikilocytosis, hypochromia
karyorrhexis, toxic granularity, vacuolization
26
Multiple Choice
Reasons for absolute erythrocytosis:
decompression sickness, blood loss
chronic hypoventilation of the lungs
hypervolemia, poisoning
hyperoxia, hemolysis
dehydration
27
Multiple Choice
In childhood, the following are more common:
acute lymphoblastic leukemia
chronic myeloid leukemia
chronic lymphocytic leukemia
acute monocytic leukemia
lymphagranulomatosis
28
Multiple Choice
In a 52-year-old woman, examination revealed a decrease in the number of erythrocytes in the blood and an increase in the level of free hemoglobin in the blood plasma (hemoglobinemia). CPU - 0.85. What type of anemia does the patient have?
hereditary hemolytic
acquired hemolytic
acute post-hemorrhagic
chronic post-hemorrhagic
anemia due to impaired erythropoiesis
29
Multiple Choice
Along with normal types of hemoglobin in the body of an adult, pathological ones may be present. Specify one of them:
HbF
HbA1
HbA2
HbS
HbO2
30
Multiple Choice
A 65-year-old patient with long-term complaints typical of chronic gastritis has megalocytes in the peripheral blood and megaloblastic erythropoiesis in the bone marrow. What is the most likely diagnosis?
aplastic anemia
hypoplastic anemia
hemolytic anemia
B12-folate deficiency anemia
Iron-deficiency anemia
31
Multiple Choice
Examination in the patient's blood revealed leukocytosis, lymphocytosis, Botkin-Gumprecht cells against the background of anemia. What disease should you think about?
chronic lymphocytic leukemia
acute myeloid leukemia
lymphogranulomatosis
Infectious mononucleosis
multiple myeloma
32
Multiple Choice
A 37-year-old patient came to the clinic with complaints of headache, dizziness, poor sleep, numbness of the extremities. For the last 6 years he has been working at a gas-discharge lamp factory in a lead workshop. In the blood: the amount of hemoglobin and erythrocytes is reduced, the content of serum iron is increased several times. Name the type of anemia:
iron deficiency
Minkowski-Shoffard anemia
iron refractory
Hypoplastic
metaplastic
33
Multiple Choice
In the blood of a 26-year-old man, 18% of erythrocytes of spherical, flattened, spherical and spinous forms were found. Other red blood cells were in the form of biconcave discs. What is the name of such a phenomenon?
cathological poikilocytosis
physiological anisocytosis
cathological anisocytosis
erythrocytosis
physiological poikilocytosis
34
Multiple Choice
The patient was diagnosed with chronic atrophic gastritis, accompanied by a deficiency of the internal Castle factor. What anemia did the patient develop?
iron refractory
hemolytic
iron deficiency
12-deficit
protein deficient
35
Multiple Choice
In humans, 10 minutes after the start of intense physical activity, the number of erythrocytes in the blood increased from 4.0x1012 / l to 4.5x1012 / l. What is causing this?
suppression of destruction of erythrocytes
exit of erythrocytes from the depot
activation of erythropoiesis
increase in minute blood volume
body water loss
36
Multiple Choice
The inflammatory process in human tissues and organs is accompanied by their hyperemia and edema. What leukocytes in the connective tissue ensure the expansion of blood vessels and increase their permeability?
neutrophils
eosinophils
basophils
T-lymphocytes
B-lymphocytes
37
Multiple Choice
A biochemical analysis of the infant's erythrocytes revealed a pronounced deficiency of glutathione peroxidase and a low level of reduced glutathione. What pathological condition can this child develop?
hemolytic anemia
cernizial anemia
haloblastic anemia
sickle cell anemia
Iron-deficiency anemia
38
Multiple Choice
The woman notes general and muscle weakness, shortness of breath, dizziness, brittle hair and nails, desire to eat chalk. A history of uterine fibroids. In the blood: er. - 2, 8 x1012 / l, Hb - 80 g / l, color index - 0.78, anisocytosis, poikilocytosis, serum iron - 10 мmol / l. What is the most probable diagnosis for this patient?
12-deficiency anemia
autoimmune hemolytic anemia
iron deficiency anemia
aplastic anemia
hypoplastic anemia
39
Multiple Choice
A 22-year-old female patient with reduced nutritional status, a vegetarian, went to the clinic with complaints of perversion of smell and taste, "sticking" in the corners of the mouth. Objectively: pronounced blueness of the sclera. Was diagnosed with iron deficiency anemia. What clinical syndrome prevails?
anemic
gemological
hemolytic
sideropenic
myelodysplastic
40
Multiple Choice
A 43-year-old man during a medical examination objectively revealed pallor of the skin and mucous membranes, flattened papillae of the tongue, transverse striation of nails, cracks in the corners of the mouth, tachycardia. The content of hemoglobin in the blood is 90 g / l, anisocytosis, poikilocytosis. The most likely causative factor for this condition is insufficient intake:
copper
iron
zinc
magnesium
Selene
41
Multiple Choice
A 18-year-old patient complains of the periodic appearance of an icteric skin color, lethargy, heaviness in the left hypochondrium. Objectively: the lymph nodes are not enlarged, the liver is near the edge of the costal arch, the spleen is +3 cm. In the blood: erythrocytes - 2, 7 1012 / l, Нb - 84 g / l, CP - 0.96, reticulocytes - 18%, erythrokaryocytes, microspherocytes ... Indirect bilirubin - 32 мmol / L. In urine - hemosiderin. The iron content in the blood serum is 23.5 mmol / l. What is the most likely diagnosis?
Minkowski-Shoffard anemia
autoimmune hemolytic anemia
sideroachrestic anemia
hypoplastic anemia
folate deficiency anemia
42
Multiple Choice
The mother of a 9-month-old child complains of significant pallor, poor appetite, and an enlarged baby's belly. At the neonatal age, the child was treated in a hospital for jaundice and anemia. Objectively: the skin is pale with an icteric tinge, there are no teeth, the abdomen is enlarged, the spleen is palpable. Hb - 90 g / l, er. - 3.0 x1012 / l, CP - 0.9, microspherocytosis, reticulocytosis up to 20%, serum bilirubin - 37 мmol / l, indirect - 28 мmol / l. What type of anemia is there?
Iron-deficiency anemia
protein deficiency anemia
12-deficiency anemia
hemolytic anemia
hereditary elliptocytosis
43
Multiple Choice
A 3-year-old child was admitted with complaints of leg pain, fever, poor appetite. Objectively: pallor of the skin and mucous membranes, hemorrhagic eruptions. The lymph nodes are enlarged, of a densely elastic consistency, not welded, painless. Pain in bones and joints, in the abdomen. The liver and spleen are enlarged. In the hemogram: hemoglobin - 88 g / l, CP - 1.3, platelets – 80 x 109 / l, leukocytes - 25,8 x109 / l, lymphoblasts - 70%, erythrocyte sedimentation rate - 52 mm / h. What is the preliminary diagnosis?
thrombocytopenic purpura
acute leukemia
acute rheumatic fever
Infectious mononucleosis
hemorrhagic vasculitis
44
Multiple Choice
An 18-year-old female patient consulted a doctor due to severe weakness, fever, progressive weight loss, and dizziness. Objectively: with a height of 165 cm, weight - 40 kg, the skin is pale with a yellowish tinge, dry, peeling. In the blood: erythrocytes - 1.8 x 1012 / l, Hb - 85 g / l, leukocytes 500 x 109 / l, formula: myeloblasts - 78%, neutrophils - 15%, lymphocytes - 7%. What is the most likely diagnosis?
acute lymphoblastic leukemia
chronic lymphoblastic leukemia
acute myeloid leukemia
chronic anemia
leukemoid reaction
45
Multiple Choice
The patient visited a dentist for tooth extraction. After tooth extraction, bleeding from the tooth cell did not stop for 15 minutes. It is known from the anamnesis that the patient suffers from chronic active hepatitis. What is the possible cause of the prolonged bleeding time?
thrombocytopenia
hypocalcemia
increased activity of the anticoagulant system
a decrease in the content of albumin in the blood
lowering the content of fibrinogen in the blood
46
Multiple Choice
The blood test of the athlete revealed: erythrocyte content - 5, 5 x1012 / l, hemoglobin - 180 g / l, leukocytes - 7 x109 / l, neutrophils - 64%, basophils - 0.5%, eosinophils - 0.5 %, monocytes - 8%, lymphocytes - 27%. Such indicators indicate the stimulation, first of all, of such a process:
leukopoiesis
erythropoiesis
lymphopoiesis
granulocytopoiesis
immunogenesis
47
Multiple Choice
The patient has a helminthic invasion by a wide tapeworm. In the analysis: hemoglobin - 95 g / l, erythrocytes - 2.8 x 1012 / l, reticulocytes - 0.5%, megalocytes and megaloblasts were found. Determine the nature of anemia
vitamin B-12– deficiency anemia
hemolytic anemia
Iron-deficiency anemia
sideroachrestic anemia
hypoplastic anemia
48
Multiple Choice
What is not typical for folate deficiency anemia:
hyperchromia of erythrocytes
leukopenia and thrombocytopenia
symptoms of funicular myelosis
atrophic glossitis
high percentage of ineffective erythropoiesis
49
Multiple Choice
The main mechanism of pathological leukocytosis is
stimulation of leukopoiesis
redistribution of blood in the vascular bed
emigration of leukocytes
diapedesis of leukocytes
phagocytosis of leukocytes
50
Multiple Choice
The nuclear shift of the leukocyte formula to the left indicates (about)
increase in the percentage of segmented neutrophils
an increase in the percentage of lymphocytes and monocytes
decrease in the percentage of young forms of neutrophils
an increase in the percentage of young neutrophils (metamyelocytes and stab)
a decrease in the percentage of lymphocytes and monocytes
51
Multiple Choice
Long-term use of cytostatics leads to
monocytosis
lymphocytosis
eosinophilia
basopenia
neutropenia
52
Multiple Choice
Tumor disease of the blood system with diffuse damage to hematopoietic tissue is called
hematosarcoma
leukemia
leukemoid reaction
agranulocytosis
pernicious anemia
53
Multiple Choice
The predominance of blast forms of granulocytes in the blood and the absence of intermediate forms of maturation with a small number of mature cells are characteristic
for chronic leukemia
for leukemoid reaction
for acute leukemia
for leukocytosis
for leukopenia
54
Multiple Choice
For leukemoid reactions of the neutrophilic type,
basophilic-eosinophilic association
the appearance of plasma cells in the blood
cellular atypism of granulocytes
hyperregenerative shift of the leukocyte formula to the left
pancytopenia
55
Multiple Choice
The total number of leukocytes is 70 x 10x109 / l; myeloblasts - 1%;
promyelocytes - 3%; myelocytes - 8%; metamyelocytes - 8%;
stab neutrophils - 15%; segmented neutrophils -36%; basophils - 2%; eosinophils -8%; monocytes - 3%; lymphocytes -16%. Leukogram indicates -
chronic myelocytic leukemia
acute lymphoblastic leukemia
acute myeloid leukemia
chronic monocytic leukemia
chronic lymphocytic leukemia
56
Multiple Choice
The content of erythrocytes in the blood of a resident of the highlands is 6.5 x 1012/ l. The mechanism of erythrocytosis development in these conditions?
activation of aortic chemoreceptors
activation of erythropoiesis
decrease in blood depot volume
activation of blood transport function
increased life span of red blood cells
57
Multiple Choice
What group of anemias does marching hemoglobinuria belong to?
toxicohemolytic
immunohemolytic
acute post-hemorrhagic
mechanical hemolytic
metaplastic
58
Multiple Choice
Erythremia (polycythemia vera) is:
intravascular hemolysis of erythrocytes
a type of chronic leukemia
atrophy of hematopoietic tissue
bone marrow inflammation
an increase in reticulocytes in the blood
59
Multiple Choice
The change from the embryonic (megaloblastic) type of hematopoiesis to the eritroblastic type occurs:
in childhood
during pregnancy
during puberty
in adults
in old age
60
Multiple Choice
The clinical picture of B12-deficiency anemia includes a triad, a component of which is funicular myelosis. The mechanism of its development?
violation of myelin synthesis
termination of axonal transport
decrease in the synthesis of neurotransmitters
decreased sensitivity of cholinergic receptors
decreased sensitivity of adrenergic receptors
61
Multiple Choice
Show regenerative forms of erythrocytes:
Jolly's bodies, normoblasts, anisocytosis
normoblasts, basophilic granularity of erythrocytes
reticulocytes, normoblasts, polychromatophilia
poikilocytosis, polychromotophilia, normoblasts
megalocytes, cabo rings, reticulocytes
62
Multiple Choice
Indicate the reasons for the appearance of megaloblasts and megalocytes in the peripheral blood:
a sharp inhibition of bone marrow function
diseases of the stomach, liver, kidneys
massive blood loss, malnutrition
lack of vitamin B12, folic acid
violation of the production of erythropoietins
63
Multiple Choice
Pathogenesis of hemolytic anemias:
transfusion of incompatible blood
increased hemolysis of erythrocytes
phenylhydrazine poisoning
increase in indirect bilirubin
enlarged spleen, jaundice
64
Multiple Choice
Iron deficiency anemia is caused by:
decrease in erythropoietin production
acute hemolysis of erythrocytes
massive hemorrhages
increased iron consumption
folate deficiency
65
Multiple Choice
Pathogenesis of hypochromia in iron deficiency anemia:
disorders of hemoglobin synthesis
violation of absorption and deposit of iron
loss of iron from the body
lack of globin and heme
lack of intrinsic Castle factor
66
Multiple Choice
Indicate the pathogenesis of clinical signs in the first hours after acute blood loss:
shortness of breath, hypoxic hypoxia
tachycardia, blood deposition
circulatory and hemic hypoxia
hypovolemia, tachycardia
release of blood from the depot, acceleration of blood flow
67
Multiple Choice
With iron deficiency anemia in the peripheral blood is observed:
hypochromia of erythrocytes
normal hematocrit
hyperchromia of erythrocytes
the appearance of megaloblasts
neutrophilic leukocytosis
68
Multiple Choice
Leukemia causes:
intoxication of the body
ionizing radiation
infrared rays
streptococci and staphylococci
chromosome 1 aberration
69
Multiple Choice
The hydraemic stage of acute post-hemorrhagic anemia is characterized by:
reticulocytosis, polychromatophilia
the appearance of normoblasts
neutrophilic leukocytosis
hyperchromic anemia
normal hematocrit
70
Multiple Choice
Indicate a symptom characteristic of panmyelosis:
increase in the number of erythrocytes
polycythemia, bone marrow hyperplasia
change in the number of blood cells
increased granulopoiesis, thrombocytopenia
hyperplasia of hematopoietic organs
The "triggering" factor for the volum-reflex is
hypervolemia
hypovolemia
normovolemia
tachycardia
blood loss
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