Clinical Consideration - Blood Flashcards

1
Q

Define anisocytosis

A

RBCs are unequal sizes - can be detected in peripheral smears
can signify conditions = anemia and thalassemia

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2
Q

Define poikilocytosis

A

refers to the presence of piokilocytes in the blood
poikilocytes are RBC with distorted shape due to membrane abnormalities or traumatic conditions
if there is more than 10% of poikilocytes in total population = piokilocytosis

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3
Q

Define anemia

A

decrease in Hb concentration in blood for the age/sex of indiviaul

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4
Q

what are the 6 types of anemia? What do each do?

A

iron deficiency- lack of absorption/loss of iron
pernicious - lack of intrinsic factor for B12 absorptions (gastric atrophy)
hemorrhagic - loss of RBCs due to bleeding (ulcer)
hemolytic - defects in cell membrane cause rupture
thalassemia - hereditary deficiency of Hb
aplastic - destruction of bone marrow (radiation/toxins)

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5
Q

What are the common symptoms of anemia?

A

weakness/tired feeling
light headedness
palpitations
SOB

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6
Q

What is autosplenectomy?

A

complication of sickle cell disease

the spleen kills itself because it can’t handle the multiple infarcts = increases the risk of infection

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7
Q

What is Cooleys anemia

A

Cooley’s anemia is a rare, life-threatening blood disorder that requires regular transfusions and extensive medical care. The condition is inherited, which means that people with the disease received variant genes from both parents. Severe symptoms generally appear by age two and include dark urine, abnormal facial bones, and poor growth. Aside from transfusions, the condition can also be treated with a bone marrow transplant.

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8
Q

How is hereditary spherocytosis caused?

A

cause by a variety of molecular defects in the genes that code for spectrin, ankyrin, band 3 and band 4
these proteins are important for the normal shape of an RBC
when deformed = spherical shape

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9
Q

what is always compared in blood cross matching?

A

donors blood cells (RBCs) to receipeints plasma (serum)

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10
Q

what is RH system?

A

inherited independent of ABO system

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11
Q

what is RH positive?

A

antigen present on RBCs (and no antibodies)

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12
Q

where do Rh antibodies develop?

A

only in Rh - blood types and only with exposure to antigen

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13
Q

what does RhoGam do?

A

it binds to the fetal blood that leaked into mommy.

it removes the binded fetal blood before the mother can react to it

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14
Q

what is special about HbA1c?

A

it binds irreversibly to glucose

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15
Q

what is hemophilia?

A

spontaneous bleeding or after any minor trauma - nose bleeds, blood in urine, joint bleeding

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16
Q

what is hemophilia A?

A

lacks factor 8 - males only = most common

17
Q

what is hemophilia B?

A

lacks factor 9 - males

18
Q

what is hemophilia C?

A

lacks factor 11 - males and females - less severe because alternate clotting factors exist

19
Q

what is malaria trophoiziotes?

A

infected RBC can be seen in peripheral smears

20
Q

when should a bone marrow study be done?

A

recurrent fever, infection, pain, bleeding with no cause

21
Q

where are bone marrow aspirations usually done?

A

iliac crest

22
Q

what is a bone marrow biopsy?

A

take out chips of bone for analysis

23
Q

aplastic cell (like aplastic anemia marrow smear) will not have what?

A

any precursors - it will look all white

24
Q

what is acute leukoemia?

A

uncontrolled production of immature leukocytes

AML
ALL

25
Q

what is chronic leukemia?

A

accumulation of mature WBC in blood steam because they do not die!
CML
CLL

26
Q

what are the signs and symptoms of leukemia?

A

acute: pallor, fatigue, bleeding, fever, infections, bone pains in arms and legs
Chronic: liver, spleen, lymphnode enlargement

27
Q

what is a bone marrow transplant a treamtnet for?

A

leukemia, SC anemia, lymphoma, asplastic anemia (no RBC production)

28
Q

what are in neutrophils azurophilic granules?

A

elastase
collagenase
meloperoxidase

29
Q

when do sickle cells die?

A

10-20 days