Midterm - RBC Anomalies Flashcards

(30 cards)

1
Q
  • refers to erythrocytes with normal amount of hemoglobin.
  • possesses a central pallor which is about 1/3 of its
    diameter.
A

Normochromic cell

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2
Q

refers to erythrocytes wherein the central light area of the
cell is larger and paler than the normal

A

Hypochromic cell

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3
Q

red cells which have an increased hb content and wherein
the central light area is smaller than the normal

A

Hyperchromic Cell

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4
Q

This condition wherein the red cell is stained with various
shades of blue with tinges of pink.
* This is due combination of the affinity of hb to acid stain
and the affinity of RNA to the basic dye.

A

Polychromasia

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5
Q

Condition where in the red cells
appear pale

A

Hypochromasia

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6
Q

Causes of Hypochromasia

A
  • IDA (Iron
    Deficiency Anemia
  • Sideroblastic anemia
  • Thalassemia
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7
Q

Conditioned wherein the red cell is
deeply stained too abnormal
thickness of cells

A

Hyperchromasia

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8
Q

Causes of Hyperchromasia

A
  • Macrocytosis
  • Spherocytosis
  • Megaloblastic anemia
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9
Q
  • 6-8 um in diameter normal
  • Associated disease: seen in normal condition, acute post
    hemorrhagic anemia
A

Normocyte

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10
Q

larger than normal greater than 8um in size round in
shape MCV

A

Macrocyte

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11
Q
  • cell which is less than 6um in size MCV less than 80 FL
    ▪ Defect: Abnormal cytoplasmic maturation but
    normal nuclear maturation
A

Microcyte

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12
Q

large oval-shaped red cell which is 9-12um .
▪ Defect: Abnormal nuclear maturation but
normal cytoplasmic maturation

A

Megalocyte

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13
Q

Megalocytosis is found in

A
  • Megaloblastic anemias like pernicious anemia
  • Anemia
  • Vit. B12 deficiency anemia or vit B12 def.
  • D. latum infection
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14
Q

Normal cell with a biconcave disc shape with increased
surface volume surface

A

Discocyte

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15
Q

small dense RBC with few irregularly spaced projections of varying length

A

Acanthocytes (Spur Cell)

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16
Q

abnormal
membrane defect caused
by an increase
sphingomyelin and dec in
cholesterol and
phospholipid.

A

Acanthocytes (Spur Cell)

17
Q

Defect: Cell membrane is folded
* CD: Cell assumes a “Pocket book
roll” appearance or biscuit shape
* AD:
o HbSC disease
o HbCC disease
o Basically, seen in
hemoglobinopathies

A

Biscuit Cell (Folded RBC)

18
Q

Defect: Abnormal lipid content
of the membrane
* CD: cell with irregularly spaced
blunt processes, resembles
crenated RBC

19
Q

Uremia, MAHA (microangiopathic hemolytic anemia), Liver ds, DIC
(disseminated intravascular coagulation), TTP, PKD

20
Q
  • Defect: G6P def. resulting to
    accumulation of Heinz bodies
  • CD: cell w/ eccentric vacuoles
    due to the plucked-out Heinz
    body
  • ADS:
    o G6PD def.
    o HUS (hemolytic uremic syndrome)
    o MAHA (microangiopathic hemolytic anemia)
A

Blister Cell (Bite Cell)

21
Q

ATP deficiency due to
prolonged storage of
anticoagulated blood
* Pathologically- due to
abnormal lipid content of the
membrane

A

Echinocytes or Crenated Cells / Burr Cells

22
Q

CD: Cell w/ central area of
Hb surrounded by colorless
area and a peripheral ring
* These cells have increase
surface to volume ration
* ADS:
o Thalassemia
o Liver ds,
o Hemolytic anemia,
o Hemoglobinopathies like:
▪ HbSS
▪ HbCC
▪ HbDD
▪ HbEE
o Iron deficiency anemia (IDA)
o LCAT def.
o Obstructive Liver ds
o Post splenectom

23
Q

Cells appear in the
shape of a teardrop or pear
with a single short or long
protrusion due to splenic
passage

A

Teardrop Cell (Dacryocyte)

24
Q

Also known as ovalocytes

25
o Hb appears to be concentrated at the two ends of the cell leaving a normal central area of pallor. o Life span is shortened
Elliptocytes
26
small round dense cell which lacks the central pallor area usually microcytic and sphere shaped.
Spherocyte
27
* Cresent shape cell due to abnormal aggregation of HbS which gives a tendency for the cell to assume a sickle shape. * Sickle cells are thin and elongated with pointed ends and are well filled with Hb.
Sickle Cell (Drepanocytes)
28
Cell fragmentation due to trauma caused by physical and mechanical agents.
Schistocytes
29
o DIC o TTP o HUS o ECLAMPSIA
Schistocytes
30
* Mouth Cells Characterized by an elongated or slit-like area of central pallor * Caused by osmotic changes due to cation imbalance (Na,K)
Stomatocyte