Term
Identify the smaller cells in the peripheral blood (platelets). Which of the following is the correct description of their development in the BM? |
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Definition
demarcation and fragmentation of megakaryocyte cytoplasm to produce proplatelets |
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Term
This is the first stage of the red cell lineage that can be recognized in the BM, what is the cell? |
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Definition
Proerythroblast (normoblast) - nucleus is immature |
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Term
The synthesis of primary granules occurs in this BM cell. Identify the cell -what disease states is this imp in? |
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Definition
Promyelocyte -Granules show up best in this stage -These granules are imp in two major diseases – AML and bacterial infections (or any reactive condition) --Acute promyelocytic leukemia with Auer rods – a form of AML --You WON’T have granules in someone with ALL (acute lymphoblast leukemia)
Histology of promyelocyte – when you see Auer rods, you know it’s AML. You’ll see toxic granulations in neutrophils – these are prominent azurophilic granules in neutrophils |
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Term
These normal peripheral blood cells leave the blood, migrate, and then differentiate into issue such as the lungs, spleen, and liver. Name the cells. |
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Definition
Monocytes -They’re in the peripheral blood, have vacuoles in the cytoplasm -Are called macrophages in the peripheral tissue |
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Term
See a nRBC in peripheral blood smear. What's the most likely dx? |
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Definition
Severe chronic hemolytic anemia Bone marrow is stressed |
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Term
What's the normal life span of a cell with 3-5 lobes? |
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Definition
Neutrophil 6-7 hrs if it extends beyond acute stage, the chronic inflammatory cells will persist (macrophages, lymphocytes) |
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Term
This is a BM cell. It is the first cell in the non-mitotic pool for erythroid cells. What is it? |
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Definition
Orthochromatic erythroblast -It will lose its nucleus to become a reticulocyte, but will still have residual RNA (so a bluish color) -Will lose its cytoplasm when it goes through the spleen |
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Term
At what stage do eosinophil granules appear? |
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Definition
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Term
A pt has an inherited chronic hemolytic anemia and these small dense spheroidal red cells in the peripheral blood; polychromasia on the blood smear -what’s the mechanism? ; and trapped red cells in the spleen. What is the defect in the red cells?
2 possible explanations for spherocytes |
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Definition
i/c production of RBC b/c you have i/c destruction – if you don’t have polychromasia, start looking to see if BM has folate and B12 – hemolytic anemia will have reticulocytes but a deficiency anemia will not!
Acquired: autoimmune disorder. Intrinsic: hereditary spherocytosis
*Cytoskeletal abnormalities involving spectrin* Part of the overall def of hereditary spherocytosis
**spherocytes trapped in the spleen, and the two ways to get spherocytes – inherited (cytoskeletal abnormality) and acquired (autoimmune or something on the surface of the RBC the spleen doesn’t like)** |
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Term
What is polychromasia associated with? |
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Definition
reticulocytes hemolytic anemia |
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Term
In the peripheral blood using routine stains these “large” red cells (colored blue) will show: |
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Definition
Polychromasia -Large cells, blue reticulated fibers -A reticulocyte with a special stain -The spleen will phagocytose this material, and in so doing will take away some of its cytoplasm, cell gets smaller |
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Term
In the WBC diff, what is a metamyelocyte?
What cell precedes the promyelocyte in myeloid maturation? Ddx? |
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Definition
Early myeloid cell
Myeloblast -has high nuclear/cytoplasmic ratio -predominate in acute leuk -will look similar to lymphoblast unless it has granules or rods |
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Term
What does the myeloid stem cell give rise to? |
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Definition
basophil, neutrophil, eosinophil, monocyte, megakaryocyte |
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Term
A patient is asymptomatic and his CBC, Hb electrophoresis, and PBS are normal except for slight hypochromia and microcytosis. He has a normal Hb electrophoresis. He suspects he had Hb Barts at birth, but not now. His diagnosis is? |
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Definition
(remember: Hb Barts is ALPHA THALASSEMIA, d/c alpha chains – in HbF, alpha chains combine with gamma chains – gamma chains will combine to form tetramers)
*Alpha thalassemia* 1, 2, 3, or 4 gene deletion. 1 = silent carrier, 4 = hydrops fatalis -He has a mild alpha-thalassemia -Can be confused with iron deficiency -Will have normal Hb electrophoresis -Decreased alpha chains so not enough for HbA, A2, and F. So all are decreased -Hb Barts consists of four gamma chains in alpha thalassemia |
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Term
What will you see in PBS with bacterial infection? |
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Definition
segmented neutrophils (neutrophilia) toxic granulations Dohle bodies |
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Term
What are Auer rods made of? |
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Definition
Fused primary (azurophilic) granules |
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Term
Signs of megaloblastic anemia
what is a specific sub-disease? |
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Definition
Hypersegmented neutrophils Cytopenias B12, folate deficiency Macrocytic Hypercellular BM (d/c fat cells, i/c in all cell lines) - indicating ineffective erythropoiesis nuclear-cytoplasmic asynchrony
pernicious anemia (no intrinsic factor) |
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Term
A cell has a very grainy cytoplasm, obscuring the nucleus. What are the major substances in its granules? |
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Definition
Basophilic cell
Histamine, heparin |
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Term
Why can unconjugated bilirubin deposit in the brains of babies? |
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Definition
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Term
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Definition
denatured Hb
anemias, thalassemias, G6PD deficiency |
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Term
What do you see initially in PBS after treating pt with iron-def anemia? |
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Definition
RETICULOCYTES - you don't see polychromasia with iron def anemia initially, but once you give iron you'll see retic initially as BM begins proper production |
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Term
What do Howell-Jolly bodies indicate? |
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Definition
Spleen is not working properly, or Spleen can't keep up with production of RBC!
Nuclear fragments, seen in megaloblastic anemia |
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Term
Folate deficiency is associated with:
what's a difference between this condition and thalassemia? |
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Definition
Ineffective erythropoiesis -hypocellular BM, cells don't develop properly, low retic count -can be caused by jejunum resection due to Crohn's disease
In thalassemia, you have some ineffective erythropoiesis but some cells get out, so *retic count is still high*f |
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