Intro to Heme Flashcards

1
Q

4 Compartments Where Blood Exists in the Body

A
  • bone marrow
  • blood
  • lymphatic system
  • tissues
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2
Q

Blood Compositioin

A
  • formed elements: RBCs, WBCs, platelets

- plasma: water, dissolved ions, proteins

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3
Q

Where does fetal/neonatal hematopoiesis occur?

A
  • primitive hematopoietic cells at 4-5 wks gestation
  • liver at 5 weeks
  • bone marrow and thymus at 8 weeks
  • spleen 12 weeks
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4
Q

What is the primary hematopoietic organ in adults?

A
  • bone marrow
  • first the long bones (until 20 years or so)
  • then vertebrae and pelvis are active most of our lives
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5
Q

Bone Marrow Composition

A
  • stroma: sinuses lined with endothelial cells and fibroblasts
  • hematopoietic cells: stem cells become mature blood cells; must be in contact or near stroma
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6
Q

What is the normal hematopoietic process? (Think about the diagram/flow chart of blood cells)

A
  • a pluripotent stem cell becomes a myeloid or lymphoid stem cell
  • myeloid stem cell can become RBCs, platelets, WBCs, or monocytes
  • lymphoid stem cell can become T cells and B lymphocytes (plasma cells)
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7
Q

What is required for hematopoiesis to occur?

A
  • healthy bone marrow
  • hormones/cytokines (erythropoietin, thrombopoietin, etc)
  • nutritional factors: iron, folate, B12
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8
Q

Erythropoiesis

A
  • RBCs originate from myeloid stem cell
  • maturation involves synthesis and accumulation of Hgb
  • nucleus is extruded before RBC is released from marrow
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9
Q

Leukopoiesis

A
  • WBCs (except lymphocytes) originate from myeloid stem cell
  • condensation and segmentation of nucleus
  • formation of granules
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10
Q

Lymphopoiesis

A
  • lymphocytes originate from lymphoid stem cell
  • B cells mature in bone marrow
  • T cells mature in thymus
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11
Q

Thrombopoiesis

A
  • platelets are derived from megakaryocytes, which originate from myeloid stem cell
  • megakaryocyte nucleus divides, but cell does not
  • cell grows then cytoplasm falls apart –> shedded fragments are platelets
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12
Q

What are some causes of bone marrow failure?

A
  • Nutritional deficiency: B12, folate, iron
  • Marrow toxins: drugs, chemo, radiation
  • Infections: HIV, HBV, HCV, EBV, CMV
  • Marrow replacement: infections, leukemia, lymphoma
  • Autoimmune diseases
  • Primary bone marrow diseases
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13
Q

What will the MCV level be in iron deficiency?

A

MCV is low b/c RBCs are small (microcytic)

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14
Q

What will the MCV level be in B12/folate deficiency?

A

MCV is high b/c RBCs are big (macrocytic)

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15
Q

Cellularity of Bone Marrow

A
  • ratio btw fat and tissue in marrow
  • 5% cellular has very little blood making ability
  • 95% cellular may actually be too many malignant cells
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16
Q

What does pyruvate kinase do for blood cells?

A

-maintain RBC shape and deformability

17
Q

What does glucose-6-phosphate-dehydrogenase do for blood?

A

-prevent excessive oxidation of Hgb

18
Q

What does the reticulocyte count tell you?

A

-will tell difference btw decreased RBC production and increased RBC destruction

19
Q

What are some examples of microcytic anemias?

A
  • iron deficiency
  • anemia of chronic dz
  • thalassemia
  • sideroblastic anemia
20
Q

What are some examples of macrocytic anemias?

A
  • folate/B12 deficiency
  • liver dz
  • hypothyroidism
  • drugs
  • myelodysplastic syndrome
21
Q

Sxs of Anemia

A
  • fatigue
  • dyspnea
  • palpitations, tachycardia, angina
  • dizziness, lightheadedness, faintness
  • HA
  • claudication
22
Q

How is anemia classified?

A
  • decreased production

- increased destruction

23
Q

What will the retic count be if there is decreased production of RBCs? What else might be found?

A
  • low retic count

- abnormalities of WBCs or platelets

24
Q

What will the retic count be if there is increased destruction of RBCs? What else might be found?

A
  • high retic count
  • jaundice/icterus
  • elevated bili and LD
  • low haptoglobin
25
Q

Sickle Cell Disease

A
  • cells can’t make it through capillary bed
  • get stuck
  • blood backs up
  • edema and pain
26
Q

What might cause erythrocytosis?

A
  • polycythemia vera

- secondary: hypoxia, abnormal EPO production, abnormal Hgb w/ high O2 affinity