POIKILOCYTOSIS, RBC INLCUSIONS Flashcards

memorization

1
Q

Have evenly spaced round projections; central pallor area present; caused by changes in osmotic pressure’ seen in liver disease, uremia, heparin therapy, pyruvate kinase deficiency or as an artifact

A

Burr cells

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2
Q

have unevenly spaced pointed projections; lack central pallor area; caused by excessive cholesterol in the membrane; associated with alcoholic liver disease, post-splenectomy and abetalipoproteinemia

A

Acanthocytes

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3
Q

Show central areas of hemoglobin surrounded by a colorless ring and a peripheral ring of hemoglobin; cells have an increased surface-to-volume ratio; seen in liver disease, hemoglobinopathies, thalassemia, iron deficiency anemia

A

Target cells/ Codocytes/ Mexican Hat cells

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4
Q

Disk-shaped cells with a smaller volume than normal erythrocytes; cells have a decreased surface-to-volume ratio; lack a central pallor; associated with defects of the red cell membrane proteins; MCHC may be >37%; increased osmotic pressure (OFT)

A

Spherocytes

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5
Q

Frequently seen in severe injury (burns); Extreme poikilocytosis with fragmentation, microspherocytosis, and elliptocytosis; thermal sensitivity, fragments at 41-45C

A

pyropoikilocytes/ microspherocytes

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6
Q

Pear-shaped cells with one blunt projection; seen in megaloblastic anemia, thalassemias, and intramedullary hematopoiesis (myelofibrosis, myelophthisic anemia)

A

Teardrop cells/ Dacryocytes

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7
Q

Shapes vary but show thin, elongated, pointed ends and will appear crescent-shaped; usually lack a central pallor

A

Sickle cells/ Depranocytes

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8
Q

Most common cause of death in patients with sickle cell anemia

A

Infectious Crisis

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9
Q

Interior portion of cell is hollow, resembling a horn or a helmet; seen in microangiopathic hemolytic anemias (MAHA)

A

helmet cells/ horn cells/ Keratocytes

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10
Q

Damaged RBCs; fragments of various sizes and shapes are present, often with pointed projections; seen in MAHA, thermal injury, renal transplant rejection, and G6PD deficiency

A

Schistocytes/RBC fragments

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11
Q

Characterized by an elongated or slit-like area of central pallor; seen in liver disease, hereditary stomatocytosis or as artifact; caused by osmotic changes due to cation imbalance (Na/K); Rh deficiency syndrome, familial pseudohyperkalemia, cryohydrocytosis

A

Stomatocytes/ Mouth Cells

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12
Q

Cigar to egg-shaped erythrocytes; Also seen in patients with the Leach phenotype - RBCs lack Gerbich Ag and Glycoprotein C

A

Elliptocytes/ Ovalocytes

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13
Q

Usually ORTHOCHROMIC NORMOBLASTS/ metarubricyte but can appear in aby erythropoietic stage of maturation; indicated bone marrow stimulation or increased erythropoiesis

A

Nucleated RBCs

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14
Q

Normal value of nucleated RBCs in newborns

A

0-10/OIO

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15
Q

Small round DNA fragments; Usually one per cell, but can be multiple; stain dark purple to black with Wright’s stain

A

Howell-Jolly Bodies

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16
Q

Conditions where Howell-jolly Bodies can be seen

A
  1. Sickle cell anemia
  2. beta thalassemia major
  3. Hemolytic anemias
  4. Megaloblastic anemia
  5. alcoholism
  6. post-splenectomy
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17
Q

Multiple, tiny, fine and coarse inclusions (ribosomal RNA remnants) evenly dispersed throughout the cell; “blueberry bagel” appearance; stains dark blue with Wright’s stain

A

basophilic stippling

18
Q

Conditions where basophilic stippling can be seen

A
  1. thalassemia
  2. megaloblastic anemias
  3. sideroblastic anemia
  4. lead poisoning
  5. alcoholism
19
Q

Small, irregular, dark staining iron granules when stained with Wright’s stain; usually clump together at periphery of the cells. s

A

Pappenheimer bodies

20
Q

Iron granules stained with Prussian blue are called Siderotic granules. iron granules stained with Wright’s stain is called pappenheimer bodies

A. both statements are correct
B. both statements are wrong
C. 1st statement is correct, 2nd is wrong
D. 2nd Statement is correct, 1st is wrong

A

A. Both statements are correct

Prussian blue - Siderotic granules
Wright’s stain - Pappenheimer bodies

21
Q

Thin red-violet, single to multiple ring-like structures that may appear in loop of figure 8 shapes

A

Cabot rings

22
Q

Conditions where cabot rings can be seen

A
  1. Megaloblastic anemia
  2. myelodysplastic syndromes
  3. lead poisoning
23
Q

Condensed, intracellular, rod-shaped crystals

A

Hemoglobin C crystals

24
Q

‘Washington monument’ can be seen in what condition

A

Hb SC disease

25
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34
Q

Degraded hemoglobin. RBC inclusion that can only be seen using supravital stains and not with wright’s stain

A

Heinz bodies (Hb H inclusion)

34
Q

Mention malarial parasites

A

P. vivax
P. falciparum
P. malariae
P. ovale

34
Q

Conditions where Heinz bodies can be seen

A
  1. G6PD deficiency
  2. Beta-thalassemia major
  3. Hb H disease
  4. Unstable hemoglobinopathies
  5. Drug-induced anemias
35
Q

Stacking or “coining” pattern of RBCs due to abnormal or increased plasma protein

A

Rouleaux

36
Q

Characterized by clumping of erythrocytes with no pattern; occurs when erythrocytes are coated with IgM antibodies and complement

A

Agglutination

37
Q

The effect of cold agglutinins to RBCs ______ and Hb _____

A

RBCs decreased
Hb no effect

38
Q

RBC indices result when agglutination is suspected

RBC ______
Hct _____
MCV ______
MCHCH ______

A

RBC - decreased
Hct - decreased
MCV - Increased
MCHC - Increased