Anemia part 2 Flashcards

1
Q

acute blood loss can lead to

A

acute hemolysis

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2
Q

menstrual loss is what type of blood loss

A

chronic

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3
Q

with chronic bleeding or hemolysis what happens to erthyropoiesis

A

increased up to 6-8 times

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4
Q

how does anemia develop

A

rate of loss exceeds rate of erythropoesis

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5
Q

what are acute hemolytic clinical sytmpoms

A

fever, pallor jaundice

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6
Q

what are chronic hemolytic clinical symptoms

A

gallstones, abnormal bone growth

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7
Q

what are 3 lab findings for hemolytic anemias

A

increased unconjugated bilirubin
decrease serum haptoglobin concentration
increase serum LDH

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8
Q

where does extravascular hemolysis occur

A

reticuloendothelial system ( spleen, liver, bone marrow)

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9
Q

extravascular hemolysis usually occurs with what type of hemolytic anemias

A

intrinsic/inherited hemolytic anemias

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10
Q

what is seen in peripheral blood smear for peripheral hemolysis

A

spherocytes
schistocytes
reticulocytes

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11
Q

what gets released in intravascular hemolysis? what does it cause? levels of haptaglobin

A

free hemoglobin

  • hemoglobbinuria
  • hemosiderinuria
  • decreased
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12
Q

usually intravascular hemolysis occurs in association with what hemolytic anemias

A

extrinsic/aquired

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13
Q

Intrinsic hereditary hemolytic anemias defect in quantitative

A

thalassemias

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14
Q

Intrinsic hereditary hemolytic anemias: defect in RBC membrane

A

spherocytosis

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15
Q

Intrinsic hereditary hemolytic anemias: defect in RBC enzymes

A

glucose-6-phosphate dehydrogenase deficiency

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16
Q

what are normal adult hemoglobin made up of

A
Hemoglobin A (alpha, beta) 
A2 ( alpha, delta) 
F ( alpha, gamma)
17
Q

define thalassemia

A

reduced production of one or more globin chains

18
Q

who is more prone to Beta thalassemia

A

Mediterranean origin

19
Q

who is more prone to Alpha thalassemia

A

southeast Asia

china

20
Q

beta thalassemia major is decrease production of what

A

HbA ( beta)

21
Q

what chromosome is beta located

A

11

22
Q

how does beta get mutated in beta-thalassemiamajor

A

point mutations

partial deletions

23
Q

how many alleles are abnormal in Beta thalassemia

A

both

24
Q

what are 2 posssible abnormal beta globin alleles and what do they produce in beta thalassemia major

A

beta o: no beta globulin

beta +: produces reduced beta globulin

25
Q

what happens in homozygous beta thalassemia major, name the posssibilites

A

Beta 0/ beta o: no normal

beta +/ beta +: reduced beta globulin

26
Q

what happens in heterozygous beta thalassemia major, name the posssibilites

A

beta + /beta o: reduced beta globulin

27
Q

what happens at birth with beta thalassemia major

A

switch HbF to HbA

28
Q

what are clinical features in children for beta thalassemia major

A

distorted facies
hepatosplenomegaly
growth retardation

29
Q

how does one test for beta thalassemia major in a lab and what do you find

A

Hb electrophoriesis or HPLC

-compensatory increase in HbA2 and HbF

30
Q

what is seen in the peripheral blood smear for beta thalasemai major

A

nucleated rbc

teardrop cells

31
Q

what is the gene situation in beta thalassemia minor

A

one normal and one abnormal gene of beta-globin

32
Q

what is a difference between beta thalassemia minor and iron deficiency anemia

A

iron therapy improves iron deficiency but worsens beta-thalassemia