Lecture 3: Hematopoiesis and Intro to Peripheral Blood Flashcards

1
Q

Be able to draw the major hematopoietic lineages

A

Ok

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2
Q

Where does hematopoiesis occur?

A
early fetus - yolk sac
middle fetus - liver
birth - bone marrow
before puberty - all skeleton
after puberty - mostly axillary bone (torso and face)
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3
Q

What characterizes normal bone marrow histology ?

What happens to bone marrow cells as we age?

A
  • “field of flowers”, no one cell type predominates

- becomes hypocellular and has more adipose tissue

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4
Q

What are the major Hematopoietic growth factors

A

CSF (myeloids)
Cytokines
EPO (RBCs)
TPO (platelets)

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5
Q
What do these do? 
Stem cell factor (SCF)
IL3
IL6
IL2
IL2/6 together
A
  • general stimulating factor
  • general stimulating factor
  • megakaryocyte and neutrophil production
  • T cell growth factor
  • B cell growth factor
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6
Q

What do these do?
GM-CSF
G-CSF
M-CSF

A
  • formation of all leuks and reticulocytes
  • stimulates neutrophil increase, used to treat neutropenia
  • stimulates monocyte and macrophage increase
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7
Q

How does kidney disease cause anemia?

A

Kidney makes the EPO. If dysfunctional, can’t stimulate RBCs to mature = anemia

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8
Q

Progression stages of erythrocyte maturation

Be able to identify images of each stage

A

Proerythroblast - large and round, basophilic
Basophilic erythroblast - smaller, basophilic
Polychromatophilic erythroblast - basophilic ribosomes with eosinophilic cytoplasm
Normoblast - eosinophilic
Nucleated

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9
Q

What happens to reticulocyte count in hemolytic anemias?

Be able to identify reticulocyte image

A

Increased, with increased RDWs

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10
Q

Progressions stages of granulocyte maturation

Be able to identify images of each stage

A

Myeloblast - basophilic
Promyelocyte - more large granules
Myelocyte - lots of fine granules
Metamyelocyte - bean shaped eosinophilic nucleus

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11
Q

Be able to identify images of mature T cell and Plasma cell

A

Ok

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12
Q

Progression stages of platelet maturation

Be able to identify images of each stage

A

Megakaryoblast: large with kidney shaped basophilic nucleus

Megakaryocyte: large multilobal nucleus, endomitosis

Platelet: small platelets break off larger cell

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13
Q

Difference between monocyte, macrophage and activated macrophage

A

Monocyte: intravascular

Macrophage: enteres the intravascular space

Activated: specific cell macrophage (microglia, Kupffer, alveolar Ms, osteoclasts)

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14
Q
What do these measure? 
Hgb
Hct
RBC
Reticulocyte percentage
RDW
A
  • conc of Hgb
  • volume & % of RBCs
  • number of RBCs
  • % of RBCs that are reticulocytes
  • width distribution
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15
Q
What do these mean? 
MCV (Mean corpuscular volume)
MCH (Mean corpuscular hemoglobin)
MCHC (Mean corpuscular hemoglobin concentration)
RPI (Reticulocyte production index)
A
  • average volume of RBC
  • average mass of hgb
  • conc of Hgb in given volume
  • corrected reticulocyte %
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16
Q
Terminology: 
Anisocytosis
Poikilocytosis
Emia/Enia means?
Cythemia/philia/cytosis means?
A
  • increased RDW (size variation)
  • more shape variation
  • low
  • high
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17
Q

Sx of Iron deficiency anemia

Causes of iron deficiency anemia

A
  • fatigue/dizzy or weak, HA, pale/yellowness, arrythmia, SOB, CP, cold hands and feet
  • diet (cow’s milk) or decreased absorption (sprue, gastrectomy), chronic iron or blood loss
18
Q

Describe the blood smear of iron deficiency anemia

A
  • microcytotic & hypochromic, increased RDW
  • decreased MCV, MCH, MCHC, RBC, HCT and reticulocytes
  • Poikilocytosis with eliptocytes and target cells (bulls-eye looking cells)
19
Q

What types of anemia are caused by lack of iron?

A

Iron deficiency anemia
Anemia of chronic disease
Sideroblastic anemia

20
Q

What type of anemia is caused by folate or B12 deficiency?

What type of anemia is caused by drugs?

A
  • Macrocytic anemia&raquo_space;> deficient DNA synthesis

- Aplastic anemia (via pancytopenia)

21
Q

Hemoglobinopathies
G6PD deficiency
Autoimmune hemolytic anemia

A
  • Hgb synthesis problems&raquo_space;> RBC destruction
  • inability to deal with oxidant stress > hemolysis
  • autoantibodies destroying RBCs
22
Q

What are the types of microcytic anemia?

A

ITAS

IDA
Thalassemia
Anemia of Chronic Dz
Sideroblastic anemia

23
Q

What are the types of macrocytic anemia?

A
Megaloblastic anemia (low B9 or B12)
Alcoholic liver dz
24
Q

What are the types of normocytic anemia (with high reticulocyte count)?

A

GHAPS

G6PD deficiency
Hereditary Spherocytosis
Autoimmune Hemolytic Anemia
Paroxysmal Nocturnal Hemoglobinuria
Sickle-Cell anemia

*the rest is normo with low reticulocyte count

25
What is marked erythroid hyperplasia and which types of dz does it appear in? Be able to identify image
- more erythroids than myeloids in bone marrow > high reticulocyte count - seen in RBC loss, GHAPS and thalassemia
26
What are nucleated RBCs and when are they seen? Be able to identify image
- RBCs with nucleus not removed (immature) released into circulation - compensatory erythropoiesis (anemia, hypoxemia) or hypo/asplenia (sickle cell, splenectomy)
27
What is megaloblastic hyperplasia and when are they seen? Be able to identify image
- bone marrow is macrocytic, hypercellular, neutrophils are very hypersegmented - seen in macrocytic anemia
28
How does aplastic anemia affect the bone marrow? How does carcinoma/leukemia affect the bone marrow? Be able to identify in image
- bone marrow becomes hypocellular = reduced hematopoiesis | - fibrotic buildup in bone marrow >>> destroys hematopoietic activity
29
What characterizes bone marrow replacement/invasion? What are the causes? Be able to identify image
- teardrop RBCs and immature WBCs (some process is disrupting cell maturation in marrow) - tumor, infection, myelofibrosis or myeloproliferative disorder
30
What is extramedullary hematopoiesis and when does it occur?
- maturation outside the bone marrow | - compensation for abnormal hematopoiesis
31
What condition is schistocytes associated with? What condition is "bite" cells and Heinz bodies associated with? Be able to identify in image
MHA (thrombocytopenia with anemia) G6PD deficiency (oxidative stress, breaking off of Hgb)
32
What condition is polymerized Hgb associated with? What condition are spherocytes associated with? Be able to identify in image
Sickle cell anemia -hereditary spherocytosis
33
What is a left shift? What is toxic granulation?
- increased immature leukocytes (horseshoe nucleus) | - dark coarse granules form within the neutrophils (associated with left shift)
34
What is a leukemoid reaction?
WBC >50k w/o evidence of leukemia (image characterized by lots of neutrophils) -elevated alkaline phosphatase
35
What is the difference between CML and AML?
CML: WBC count ~100k (blasts in marrow increases as dz progresses >>> messes with normal hematopoiesis and results in pancytopenia) AML: myeloid blast accumulation (with Auer rods)
36
What are the causes of neutropenia?
Inadequate granulopoiesis (suppression of precursors, stem cells) Increased destruction of neutrophils (autoimmune, splenomegaly, more peripheral usage)
37
What is lymphocytosis associated with?
Leukemia (CLL in adults, ALL in kids) Be able to differentiate on image
38
How does a Mono stain present? What are the triad sx for Mono?
weird shaped/lumpy T lymphocytes triad: fever, pharyngitis, lymphadenopathy
39
What conditions are these associated with? Eosinophilic leukocytosis Basophilic leukocytosis Monocytosis
- allergy, parasites - rare, leukemia - atypical bacterial infections, autoimmune
40
What is the pathway of primary hemostasis?
Gp1b on platelet binds to von Willebrand factor on endothelium > releases ADP and thromboxane A2 > aggregation of platelets by binding fibrinogen
41
What characterizes thrombocytopenia?
low platelets | -presents with petichiae/ecchymosis
42
What are the major causes of thrombocytopenia?
increased platelet destruction (purpura, autoimmune, drug, DIC, HIV) decreased production (bone marrow or liver problem) Enlarged spleen