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

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

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
what happens in homozygous beta thalassemia major, name the posssibilites
Beta 0/ beta o: no normal | beta +/ beta +: reduced beta globulin
26
what happens in heterozygous beta thalassemia major, name the posssibilites
beta + /beta o: reduced beta globulin
27
what happens at birth with beta thalassemia major
switch HbF to HbA
28
what are clinical features in children for beta thalassemia major
distorted facies hepatosplenomegaly growth retardation
29
how does one test for beta thalassemia major in a lab and what do you find
Hb electrophoriesis or HPLC | -compensatory increase in HbA2 and HbF
30
what is seen in the peripheral blood smear for beta thalasemai major
nucleated rbc | teardrop cells
31
what is the gene situation in beta thalassemia minor
one normal and one abnormal gene of beta-globin
32
what is a difference between beta thalassemia minor and iron deficiency anemia
iron therapy improves iron deficiency but worsens beta-thalassemia