POIKILOCYTOSIS prt. 2 Flashcards

1
Q

The hallmark of hemolytic anemia secondary to red cell fragmentation is the_______, which takes several forms.

A

schistocyte

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2
Q

When a red cell attempts to pass between fibrin strands, altered vessels, or damaged heart valve prostheses, it may be cleaved and fragmented and become a_______

The erythrocyte trying to squeeze through an opening half its diameter becomes stretched and develops a blister because of the shear stress of the flowing blood.

When this cell passes through the spleen, it is fragmented into two pieces, and the membrane is less deformable. Fragmented red cells do not survive long in the circulation.

A

schistocyte

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3
Q

Schistocytes (Greek word schistos, “_____”) or schizocytes (Greek schizo, “_____”’) result from membrane damage; they are not hereditary.

A

cloven

split

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4
Q

Schistocytes include helmet, triangular, and a variety of small, irregular shapes with a few pointed extremities.

The finding of_____ and _____ is strongly suggestive of a microangio-pathic hemolytic anemia or traumatic hemolytic anemia

A

helmet and fragmented cells

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5
Q

occur in patients with severe burns, renal graft rejection, glomerulonephritis, vasculitis, thrombotic thrombocytopenic purpura, and diffuse intravascular coagulation

A

Schistocytes

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6
Q

accompanying march hemoglobinuria most likely are attributable to mechanical damage to the cells in the feet of individuals on long walking expeditions.

A

Schistocytes

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7
Q

schistocyte with one or more hornlike projections has been identified as a______ (Greek_______, “horn”)

A

keratocyte

keras

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8
Q

These cells may or may not have a normal volume and usually no area of central pallor.

A________ is the result of an erythrocyte being caught on a fibrin strand, which could cut the cell in two.

As the sides of the erythro cyte are pushed against the fibrin strand, they tend to fuse together.

When this cell escapes from the fibrin strand, it may have a vacuole-like area in the fused portion (this is known as a blister cell).

This vacuole ruptures to form the_______
— a damaged red cell with horns.

A

keratocyte

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9
Q

do not remain in circulation for more than a few hours, as they are fragile

They are a rare and interesting phenomenon.

Some morphologists report helmet cells, which actually look like a helmet, as ______

A

Keratocytes

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10
Q

pear shaped with a blunt pointed projection and
may be normal size, small, or large; “teardrops”

A

dacryocytes

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11
Q

have been so labeled because of their shape (Greek dakry, “tear”)

A

Dacryocytes (teardrops)

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12
Q

They may also be pear shaped with a blunt pointed projection and may be normal size, small, or large.

A

Dacryocytes (teardrops)

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13
Q

If a red cell contains a rigid inclusion, such as a Heinz body, the portion with the inclusion cannot pass through small openings of splenic sinuses and thus remains behind.

As the red cell squeezes through the small opening, it is stretched beyond its ability to regain its original shape.

Thus, a teardrop or pear shape is created.

A

Dacryocytes

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14
Q

typically are observed in myelofibrosis with myeloid metaplasia because of the large size of the spleen.

Other conditions with ______ include myelophthisic anemia, pernicious anemia, B-thalas-semia, drug-induced Heinz body formation, tuberculosis, and tumor metastasized to the marrow.

A

Teardrop cells
Dacrocytes

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15
Q

Red cells containing ___________________ squeeze through the splenic sinuses, hence will have its original shape STRETCHED (causing teardrop-shaped cells)

A

Heinz bodies

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16
Q

occur in severe burns as
small, round cells that may be smaller than platelets; they
are the result of thermal damage to the cell membrane.

A

Microspherocytes

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17
Q

Another name for microspherocytes

A

microspherules

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18
Q

Microspherocytes in rare hereditary HA occur at what temperature?

A

45 degrees C

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19
Q

Normocytes (normal RBCs) fragment at what temperature?

A

49 degrees C

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20
Q

T or F: MCV of those with rare hereditary HA designated pyropoikilocytosis have EXTREMELY LOW MCV

A

T

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21
Q

a large, pale-pink staining ghost of a red cell—the membrane
remaining after the contents have been released; as large as leukocytes

A

Semilunarbodies

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22
Q

Other names for semilunar bodies

A

half-moon cell/crescent cell

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23
Q

T or F: Semilunar bodies are ALWAYS acquired

A

T

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24
Q

Semilunar bodies are frequently seen in: (conditions)

A

Malaria & conditions causing overt hemolysis

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25
Q

Three types of poikilocytes characteristic of three abnormal hemoglobins (abnormal hemoglobin content)

A
  1. drepanocytes (from Hb S)
  2. Hb CC crystals
  3. Hb SC crystals
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26
Q

Three types of poikilocytes characteristic of three abnormal hemoglobins (abnormal hemoglobin content)

A
  1. drepanocytes (from Hb S)
  2. Hb CC crystals
  3. Hb SC crystals
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27
Q

cells that have been changed from the normal disc shape by the long
rod-shaped polymers of the inherited abnormal Hb S

A

Drepanocytes

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28
Q

Drepanocytes are also known as

A

sickle cells

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29
Q

A red cell does not appear sickled until it has lost its _________
and has been fully _____________.

A

nucleus; hemoglobinized

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30
Q

___________ are thin
and elongated with pointed ends and are well filled with
Hb. They may be curved or straight or have S, V, or L shapes.

A

Sickle cells/drepanocytes

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31
Q

T or F: The change in shape of drepanocytes is striking and IRREVERSIBLE secondary to permanent membrane damage by the polymerization of Hb S

A

T

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32
Q

Typical sickle cells are observed in films from patients with ______________ Hb S disease (Hb SS) but are not often
seen in ___________ Hb S (Hb AS; sickle trait) except under unusual situations when there is low in vivo oxygen tension.

A

homozygous; heterozygous

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33
Q

Meaning of drepanos

A

sickle

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34
Q

2 poikilocytes associated with malaria

A

1) semilunar bodies (poikilocyte secondary to trauma)
2) drepanocytes (poikilocyte secondary to abnormal Hgb content)

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35
Q

Drepanocytes are caused by a ________ mutation on the 6th position of amino acids (glutamic acid is changed to ________)

A

point (mutation); valine

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36
Q

intracellular crystals that are hexagonal with blunt ends and are darkly stained; these angular crystals form within the cell membrane when Hb C crystallizes

A

Hemoglobin CC crystals

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37
Q

T or F: Frequently, the cell membrane is not visible, and the crystal appears to be free (Hgb CC crystals). At times, several smaller CC crystals form within the red cell.

A

T

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38
Q

Hemoglobin CC crystals are seen in homoxygous C (Hgb CC) disease but not in _______________

A

Hemoglobin C trait (heterozygous)

39
Q

Hemoglobin CC crystals are seen in homoxygous C (Hgb CC) disease but not in _______________

A

Hemoglobin C trait (heterozygous)

40
Q

dark-hued crystals of condensed Hb that distort the red cell membrane

A

Hemoglobin SC crystals

41
Q

2 forms of Hgb SC crystals

A
  1. straight
    with parallel sides
  2. blunt, pointed, protruding end
    (“Washington monument” shape).
42
Q

multiple crystals that
protrude in different directions as finger-like projections from a common crystalline center

A

Hemoglobin SC crystals

43
Q

Identify if hemoglobin crystal is SC or CC:
1. crystal PROTRUDING membrane
2. crystal formed WITHIN cell membrane
3. Washington monument
4. Hexagonal and elongated
5. Projecting end blunt
6. both ends blunt
7. parallel sides to crystal
8. parallel sides to projection

A
  1. SC
  2. CC
  3. SC
  4. CC
  5. SC
  6. CC
  7. CC
  8. SC
44
Q

Erythrocytes with a normal Hb content have a clear central pallor that occupies about one-third of the cell diameter

A

Normochromic

45
Q

With decreasing Hgb concentration, there is __________ central pallor, these cells are termed as _________\

A

Increased; hypochromic

46
Q

Hypochromia is associated most often with __________

A

Microcytosis

47
Q

Examples of hypochromic, microcytic anemias include:

A

iron deficiency anemia, thalassemia, and sideroblastic anemia

48
Q

Hypochromia with normocytic cells conditions that result from defective macrophage iron release, which prevents iron from reaching the normoblasts for proper red
cell maturation.

A

Rheumatoid arthritis, chronic infection, inflammation

49
Q

the term used to describe the variation in Hb content when both hypochromic and normochromic cells are present.

A

Anisochromia

50
Q

Macrocytic cells usually do not have an area of central pallor because of their __________ thickness.

A

increased

51
Q

Spherocytes have reduced central concavity and no central pallor because of their _________ thickness.

A

increased

52
Q

Sickled red cells do not show normal ______________

A

central pallor

53
Q

Hemoglobin is concentrated within a _____________ in the abnormal Hb genotypes CC and SC

A

crystal

54
Q

True hyperchromia exists when the __________ is elevated

A

MCHC

55
Q

T or F: Erythrocytes normally contain inclusions

A

F!! NOOOOOOO

56
Q

Inclusions in developmental organelles:

A

Howell-Jolly bodies, basophilic stippling, Pappenheimer bodies, polychromatophilic red cells, and Cabot rings

57
Q

small, round fragments of the
nucleus (resulting from karyorrhexis or nuclear disintegration) of a late nucleated red cell or metarubricyte

A

Howell-Jolly bodies

58
Q

Howell-jolly bodies stain _________________ in Wright stain

A

reddish-blue to blue-black

59
Q

Howell-jolly bodies may also result from:

A
  1. incomplete extrusion of nucleus
  2. chromosomes that were separated from the spindle during abnormal mitosis
60
Q

Howell-jolly bodies give a _______ Feulgen reaction

A

positive

61
Q

A test for DNA in nuclear chromatin

A

Feulgen reaction

62
Q

What inclusions are increased in the blood film after splenectomy?

A

Howell-jolly bodies

63
Q

Seen in sickle cell anemia, other hemolytic anemias, megaloblastic anemia, congenital absence of spleen, splenic atrophy

A

Howell-jolly bodies

64
Q

fine or coarse, deep blue to
purple staining inclusion that appears in erythrocytes on a dried Wright-stained film; smaller than Howell-Jolly bodies, are usually irregularly shaped, and appear homogeneously throughout the Fib portion of the erythrocyte.

A

Basophilic stippling

65
Q

T or F: Basophilic stipplings do NOT exist in living cells but can be observed in well-made preparations for electron microscopy

A

T

66
Q

2 forms of basophilic stippling:

A
  1. Fine stippling
  2. Granular
67
Q

Basophilic stippling due to increased red cell population, seen with increased polychromatophilia

A

Fine stippling

68
Q

Basophilic stippling due to abnormal instability of RNA in the young cells, seen in lead poisoning, thalassemia, megaloblastic anemia, and severe anemia.

A

Granular stippling

69
Q

Siderotic granules that are small, irregular, dark-staining granules that appear near the periphery of a young erythrocyte in a film stained with Wright or supravital stain

A

Pappenheimer bodies

70
Q

these bodies stain positively in Perls’ PRUSSIAN BLUE indicating their iron content

A

Pappenheimer

71
Q

An erythrocyte that is positive for siderotic (iron) granules
in a Prussian blue stain is designated a __________

A

siderocyte

72
Q

A normoblast (nucleated erythrocyte) with siderotic
granules is called a _____________.

A

sideroblast

73
Q

Pappenheimer: Normally no more than
_____ small iron particles are noted in developing nucleated red cells in bone marrow.

A

3

74
Q

Siderotic granules in normal sideroblasts and siderocytes represent dispersed _______ (a storage form of iron) molecules.

A

ferritin

75
Q

The ________ is thus responsible for removing excess iron-containing granules from young red cells in
which Hb synthesis is complete.

A

spleen

76
Q

On a Wright-stained film it is possible to misidentify Pappenheimer bodies as ______________ when the
iron overload is severe

A

basophilic stippling

77
Q

A thin ringlike structure called a _____________ may appear in erythrocytes in megaloblastic anemia
or other severe anemias, in lead poisoning, and in dys-
erythropoiesis, in which erythrocytes are destroyed before being released in the bone marrow

A

Cabot ring

78
Q

What are the 2 inclusions associated with or are present in lead poisoning?

A

Basophilic stipplings, Cabot rings

79
Q

Inclusions that may be circular
and appear at the cell periphery, or it may form a figure eight, incomplete rings, or other configurations.

A

Cabot rings

80
Q

round, refractile inclusions not visible
on a Wright-stained film. They range in size from about 1 to 3 um and are attached to the erythrocyte membrane; if in multiples, may appear as pitted golf ball

A

Heinz bodies

81
Q

Heinz bodies are best identified by supravital staining with basic dyes such as:

A

crystal violet, methylene
blue, or brilliant cresyl blue

82
Q

_____________ consist of denatured globin derived from destruction of the Hb molecule. These inclusions are not seen in normal individuals (unless the person is acutely poisoned) because they are pitted out by the spleen.

A

Heinz bodies

83
Q

Heinz bodies are produced in the blood of normal persons who have been poisoned by:

A

aromatic nitro-com-
pounds, amino-compounds, and inorganic oxidizing agents used in treatment protocols

84
Q

Heinz bodies also occur in individuals with a hereditary
deficiency of the enzymes _________ or glutathione as a result of exposure to
drugs or agents containing the above compounds

A

glucose-6-phosphate dehydrogenase (G6PD)

85
Q

Heinz bodies also occur in individuals with a hereditary
deficiency of the enzymes _________ or glutathione as a result of exposure to
drugs or agents containing the above compounds

A

glucose-6-phosphate dehydrogenase (G6PD)

86
Q

Plasmodium spp. are transmitted to man by _________

A

Anopheles mosquitoes

87
Q

4 plasmodium species that cause malaria

A
  1. P. vivax
  2. P. malariae
  3. P. falciparum
  4. P. ovale

(VilMa FOntanilla)

88
Q

Schuffner’s stipplings; 4 maturation stages infects the RBC (become enlarged)

A

P. vivax (Vilma Santos)

89
Q

RBC not enlarged; Ziemann’s dots

A

P. malariae (Manila Zoo)

90
Q

Small delicate ring forms, gametocytes are banana shaped; Maurer’s dots

A

P. falciparum (Ferdinand Marcos)

91
Q

RBC is oval; James dots

A

P. ovale (Orange Juice)

92
Q

forms ringlike structures resem¬
bling the ring stages of malarial parasites; round, oval, elongated, amoeboid, or pear-shaped
and are often tiny, ranging in size from 1 to 5 um; appears as tiny rings with minimal blue tufts of cytoplasm and a little dot of chromatin. Reproduction occurs asexually
by a division that results in a tetrad of organisms that somewhat resembles a cross.

A

Babesia

93
Q

Red cells infected with Babesia are ___________, and pigment is not present

A

Not enlarged