Pathology of Red Blood Cells and Bleeding Disorders (Part 2 of 3) Flashcards

1
Q

what causes megaloblastic anemia?

A

impaired DNA synthesis

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2
Q

what happens in the bone marrow as a result of impaired DNA synthesis?

A

growth factors signal for increased production and marrow hyperplasia occurs, but hematopoiesis is still ineffective

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3
Q

what is the MCV like in megaloblastic anemia?

A

it is high

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4
Q

what are the characteristics of megaloblastic anemia (HGB, HCT, MCV, and reticulocyte count)

A

low HGB, low HCT, high MCV, and low reticulocyte count

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5
Q

what does the peripheral blood smear look like in megaloblastic anemia? ( type of anemia, cell shape, neutrophils)

A

hypoproliferative anemia, macrocytic anemia, ovalocyte shape RBCs, and neutrophil hypersegmentation

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6
Q

what are two common causes of megaloblastic anemia?

A

B12 and folate deficiencies

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7
Q

what is pernicious anemia?

A

when lymphocytes are directed against gastric parietal cells, which are responsible for secretion of intrinsic factor and intrinsic factor is required for B12 absorption; it is associated with B12 anemia

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8
Q

what are the results of pernicious anemia?

A

chronic atrophic gastritis, megaloblastic anemia, atrophic glossitis, spinal demyelination

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9
Q

what neural issues can be seen in pernicious anemia?

A

paresthesias, gait disturbances, altered vision, taste, smell, dementia, and psychosis

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10
Q

diagnosis of pernicious anemia can involve what? (4)

A

megaloblastic anemia, low b12, IF antibodies, and high levels of homocysteine/MM Co-A

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11
Q

what could block the metabolism of folate leading to folate deficiency?

A

methotrexate (inhibits DHF reductase)

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12
Q

diagnosis of folate deficiency can involve? (3)

A

megaloblastic anemia, low red cell folate, and high levels of homocysteine

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13
Q

what type of anemia does iron deficiency cause?

A

hypochromic microcytic anemia

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14
Q

what carries iron to the marrow or into storage?

A

transferrin

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15
Q

in storage sites, what is iron incorporated into?

A

ferritin

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16
Q

in marrow, what is iron incorporated into?

A

into Hgb for red cells

17
Q

the control of iron happens at what level?

A

at the absorption level

18
Q

what influences the tipping point between storing the iron or allowing it through the ferroportin channel into the transferrin systemic pool?

A

hepcidin

19
Q

what happens when plasma iron is low?

A

hepcidin backs off and ferroportin can take those iron molecules out of the mucosa and put it into the trasferrin pool

20
Q

what happens when there is high plasma iron?

A

hepcidin destroys ferroportin

21
Q

what does the peripheral smear look like in iron deficiency anemia?

A

hypoproliferative, microcytic, and hypochromic; anisocytosis

22
Q

what are the etiologies of iron deficiency anemia?

A

dietary lack, impaired absorption, increased requirement, and chronic blood loss

23
Q

what is the first stage of iron deficiency?

A

reduced ferritin

24
Q

what are the physical manifestations of IDA?

A

koilonychia, alopecia, atrophic glossitis, angular cheilitis

25
Q

what are the iron studies consistent with iron deficiency anemia?

A

low serum iron, low serum ferritin, increased TIBC, and low hepcidin

26
Q

what is anemia of chronic disease?

A

impaired red blood cell production/ iron utilization in chronic illness such as infection, immune diseases, and malignancy

27
Q

what are the two mechanisms involved in anemia of chronic disease?

A

inflammatory cytokines increase hepcidin and low erythropoietin

28
Q

what are the features of anemia of chronic disease?

A

low serum iron, reduced TIBC, increased serum ferritin, and abundant stainable iron in tissues

29
Q

what is aplastic anemia most commonly due to?

A

drugs, irradiation, and viral infection

30
Q

what rare inherited forms cause aplastic anemia?

A

Fanconi anemia (DNA repair defect)

31
Q

how do you make the diagnosis of aplastic anemia?

A

the presentation will be along the lines of pancytopenia: anemia, thrombocytopenia, and leukopenia

32
Q

what will the anemia be like in aplastic anemia?

A

normocytic but no retic count

33
Q

where do you make the definitive diagnosis of aplastic anemia?

A

in the bone marrow

34
Q

what is pure red cell aplasia?

A

when the bone marrow shoes decreased/abnormal erythroid precursors

35
Q

when might pure red cell aplasia be seen?

A

seen in autoimmune phenomena such as thymoma

36
Q

what is myelophthisic anemia?

A

space occupation in the marrow (like metastatic cancer, fibrosis, inflammation, necrosis) replace normal hematopoietic cells

37
Q

what occurs in myelophthisic anemia?

A

abnormal release of erythroid and granulocyte precursors results in leukoerythroblastosis