Exam 1 Material Flashcards

1
Q

Acanthocyte

Morphology
Condition(s) associated with:

A

No area of central pallor
Sharp, irregular projections

Abetalipoproteinemia (heredity)

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2
Q

Blister cell

Morphology:
Condition(s) associated with:

A

Inclusion within cell that spleen has pitted out; membrane heals around where inclusion is located

Any condition that has inclusion bodies in RBCs

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3
Q

Burr Cells/Echniocytes

Morphology:
Condition(s) associated with:

A

Central pallor present
Uniform-spaced projections

HUS (Hemolytic Uremic Syndrome)
PK (Pyruvate Kidney Deficiency)

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4
Q

Crenation

Morphology:
Condition(s) associated with:

A

Central pallor present
Similar to Burr cells/echinocytes, but might have “slightly” spiker projections

Commonly a drying artifact
Can be seen with a patient with severe electrolyte imbalance

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5
Q

Elliptocytes

Morphology:
Condition(s) associated with:

A

Pencil/Cigar-shaped cells

Hereditary Elliptocytosis

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6
Q

Hemoglobin C Crystals

Morphology:
Condition(s) associated with:

A

Intracellular “bars of gold”

Hemoglobin C disease (homozygous Hgb C)

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7
Q

Hemoglobin SC crystals

Morphology:
Condition(s) associated with:

A

“Glove/Mitten cells” “Pointed Finger” “Elbow Cells”

Hemoglobin SC disease (heterozygous HgB S & C)

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8
Q

Macroovalocytes

Morphology:
Condition(s) associated with:

A

Egg/Oval-shaped

Megaloblastic anemia (i.e. folate and B12 deficiency, pernicious anemia)

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9
Q

Round Macrocytes

Morphology:
Condition(s) associated with:

A

Round, larger then normal RBCs

Liver disease, Reticulocytosis

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10
Q

RBC Clumps/Agglutination

Morphology:
Condition(s) associated with:

A

Clumps of RBCs

Antigen-Antibody reaction
(some) Hemolytic anemias

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11
Q

Rouleaux

Morphology:
Condition(s) associated with:

A

Stacking of RBCs “Coins”

Multiple Myeloma

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12
Q

Schistocytes

Morphology:
Condition(s) associated with:

A

Fragmented RBCs

Burn Patients
DIC
TTP
Hemolytic anemia

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13
Q

Sickle Cells

Morphology:
Condition(s) associated with:

A

Elongated with pointed ends

Sickle Cell disease (Homozygous Hgb SS)

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14
Q

Spherocytes

Morphology:
Condition(s) associated with:

A

Dark, dense
No central pallor

Heredity spherocytosis
Transfusion of old blood

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15
Q

Stomatocytes

Morphology:
Condition(s) associated with:

A

Slit-like area through the central pallor

Rh null disease
Heredity stomatocytosis
Commonly a drying artifact

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16
Q

Target cells

Morphology:
Condition(s) associated with:

A

“Bull’s eye”

Thalassemias
Hemglobinpathies

17
Q

Teardrop cells

Morphology:
Condition(s) associated with:

A

Teardrop-shaped

Tumor in BM
Myelofibrosis

18
Q

Mixed Cell Population

Morphology:
Condition(s) associated with:

A

2 distinct RBC populations

Transfusion Therapy

19
Q

Basophillic Strippling

Morphology:
Composition:
Condition(s) associated with:

A

Speckled-bluish dots throughout the cell

Altered RNA

Lead poisoning, Thalassemia

20
Q

Howell-Jolly Bodies

Morphology:
Composition:
Condition(s) associated with:

A

Round, purple dots

DNA

Sickle Cell, Megaloblastic anemia, post-splenectomy

21
Q

Pappenheimer Bodies

Morphology:
Composition:
Condition(s) associated with:

A

Clumps or Clusters

Non-heme iron

Thalassemia, Sideroblastic anemia

22
Q

Heinz Bodies

Morphology:
Composition:
Condition(s) associated with:

A

Roundish granules at the end of a blood cell

Precipitated Hgb

G6-PD disease

23
Q

Cabot Rings

Morphology:
Composition:
Condition(s) associated with:

A

“Figure 8”

remnants of Mitotic spindle

Pernicious anemia, lead poisoning