RBC anomalies Flashcards

1
Q

increased number of red cells with variation in size

A

Anisocytosis

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2
Q

normal RBCs diameter

A

7-8um

80-100 fL

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3
Q

-associated with impaired DNA synthesis

A

Macrocytes

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4
Q

associated with defective hemoglobin formation

A

microcytes

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5
Q

Four ways to detect anisocytosis:

A

1) nucleus of a lymphocyte
2) MCV value
3) RDW value
4) RBC histogram

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6
Q

a calculated index (from the RBC histogram) given by hematology analyzers to
help identify anisocytosis and provide information about its degree

A

red cell distribution width (RDW)

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7
Q

DERIVATION OF RDW-CV

A

A - Beckman Coulter, Inc

B - Sysmex Corporation

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8
Q

RDW ref. range for newborns

A

14.2% to 19.9%

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9
Q

visual display of cell size in RBC histogram

A

X-axis

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10
Q

cell frequency or the number of cells in RBC histogram

A

Y-axis

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11
Q

two parameters calculated from RBC histogram

A

: MCV and RDW

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12
Q

shift to the right.

A

RBCs are macrocytic,

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13
Q

shift to the left

A

RBCs are microcytic

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14
Q

bimodal

A

two populations of RBCs in the sample

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15
Q

wider or flattened curve on a histogram indicates

A

more variation in the size of the cells

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16
Q

General term for a variation in the normal coloratio

A

anisochromia

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17
Q

occurrence of hypochromic cells and normochromic cells in the same blood smear

A

anisochromia

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18
Q

hypocrhomic cells

A

central pallor 1/3 of diameter (microcytic)

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19
Q

grading of hypochromia 4+

A

thin rim of hemoglobin

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20
Q

Pesary cell/ghost cell

A

Anulocyte

-thin rim of Hgb

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21
Q

RBCs that lack central pallor even though they lie in a desirable area for evaluation

A

Hyperchromic cells

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22
Q

basically the only disease in which the MCHC is high

A

Hereditary Spherocytosis

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23
Q

symptomatic HS 3 clinical manifestation

A

1) Splenomegaly
2) Anemia
3) Jaundice

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24
Q

HS MCHC value

A

35-38 g/dL

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25
more sensitive alternative test for confirmation of HS.
EMA binding test
26
larger than normal red cells with bluish tinge (Wright’s stain)
Polychromatophilic erythrocytes
27
bluish tinge in Polychromatophilic erythrocytes
residual RNA
28
increased number of red cells with variation in SHAPE
Poikilocytosis
29
Almost spherical in shape | Lacks the central pallor
SPHEROCYTE
30
STOMATOCYTE aka
Mouth cell
31
Elongated RBCs with a slit-like | central pallo
STOMATOCYTE
32
-most common form of stomatocytosis
Dehydrated hereditary | stomatocytosi
33
appears to have puddled at one end
Dehydrated hereditary | stomatocytosi
34
ACANTHOCYTE aka
thorn cell/spur cell
35
RBCs with irregularly | spiculated surface
ACANTHOCYTE
36
Abetalipoproteinemia aka
Bassen-Kornzweig syndrome | & Hereditary acanthocytosis
37
characterized by defective apo B synthesis
Abetalipoproteinemia
38
what are NOT | found in plasma in Abetalipoproteinemia
VLDL, LDL, and | chylomicron:
39
McLeaod syndrome(kell bld group)
ACANTHOCYTE
40
BURR CELL aka
Echinocyte
41
RBCs with | regularly spiculated surface
BURR CELL
42
BURR CELL associated with
Uremia | & Pyruvate kinase deficiency
43
hereditary leptocytosis
Elliptocyte
44
Elliptical (cigar-shaped) RBC
Elliptocyte
45
DACRYOCYTE aka
teardrop/pear-shaped
46
Primary Myelofibrosis (PMF)
dacryocytes
47
Fragmented RBC
schistocytes/schizocytes
48
DIC tests
D-dimer test | PF 1+2
49
DIC related conditions
" TOMASA " ``` Tissue trauma Obstetric complications Mucus-secreting tumors Acute infections Snake bites Acute promyelocytic leukemia ```
50
Drepanocyte aka
Sickle cell/ meniscocyte
51
sickle/crescentshaped
Drepanocyte
52
Two forms of drepanocyte
1) irreversible sickle cells (ISC) | 2) Oat-shaped cell
53
no capacity to return to normal shape
irreversible sickle cells (ISC)
54
once oxygenated can go back to original form
oat cell
55
RBCs which show a centrally stained area with a thin outer rim of hemoglobin
LEPTOCYTE
56
LEPTOCYTE aka
codocyte, platycyte, Greek helmet cell, mexican hat cell, Bull's eye cell, target cell
57
leptocyte associated with
liver disease, certain hemoglobinopathies, Thalassemia LCAT deficiency
58
BITE CELL aka
Degmacyte
59
Glucose-6-Phosphate Dehydrogenase (G-6-PD) deficiency poikilocyte
BITE CELL
60
Demonstrate a semicircular defect in their edge (resembles a bite mark)
BITE CELL
61
Folded RBCs
BISCUIT CELL
62
Hemoglobin SC disease
BISCUIT CELL
63
BRONZE ELLIPTOCYTE associated with
Sickle cell anemia
64
Bipolar or central distribution of | hemoglobin
BRONZE ELLIPTOCYTE
65
-As large as leukocytes -Pale-pink staining ghost of the red cell
SEMILUNAR BODY
66
associated with malaria and overt hemolysis
semilunar body
67
punctate basophilia
basophilic stippling
68
aggregated RNA
basophilic stippling
69
basophilic stippling associated with
- Lead poisoning (plumbism) | - megaloblastic anemia
70
2 forms of basophilic stippling
1) fine stippling - polychromatophilia | 2) coarse stippling -
71
iron stains
siderotic granules
72
NMB, Wright stain
Pappenheimer bodies
73
Pappenheimer bodies
SIDEROTIC GRANULES
74
dimorphic peripheral blood picture
Sideroblastic anemia
75
Remnants of nuclear chroma | tin (DNA)
HOWELL-JOLLY BODIES
76
HOWELL-JOLLY BODIES associated
- Megaloblastic anemias - After splenectomy - Thalassemia
77
histochem staining reaction for DNA
Feulgen reaction (+)
78
THREADLIKE/ MITOTIC SPINDLES
CABOT RINGS
79
Denatured and | precipitated hemoglobin
HEINZ BODIES
80
-Glucose-6-Phosphate Dehydrogenase (G-6-PD) deficiency inclusion body
HEINZ BODIES
81
supravital stains for HEINZ BODIES
NMB BCB Crystal violet methyl violet
82
eccentrically along the inner RBC membrane, large, round, blue to purple materials)
HEINZ BODIES
83
Precipitated Hb H
Hb H inclusion bodies
84
Hgb H disease is associated with
Alpha thalassemia
85
Appearance of RBCs with Hb H Bodies:
pitted golf balls
86
graded as : 1 + = 1 to 5 per field 2 + = 6 to 10 per field 3 + = greater than 10 per field
``` Polychromatophilia Helmet cells (helmet-shaped schistocytes) Dacryocytes (teardrop cells) Acanthocytes (thorn or spur cells) Schistocytes (fragmented RBCs) Spherocytes ```
87
1 + = 3 to 10 per field 2 + = 11 to 20 per field 3 + = greater than 20 per field
``` Poikilocytosis Ovalocytes Elliptocytes Burr cells Bizarre-shaped RBC Target cells (codocytes/leptocytes/bull’s eye cell/ Mexican hat cells/Greek helmet cells/platycytes) Stomatocytes (mouth cells) ```
88
pseudoagglutination aka
Rouleaux
89
Caused by a serum protein abnormality
Rouleaux
90
1 + IN ROULEAUX
= aggregates of 3 to 4 RBCs
91
2 + IN ROULEAUX
= aggregates of 5 to 10 RBCs
92
3 + IN ROULEAUX
= many aggregates with | only a few free RBCs
93
Graded as POSITIVE only
Sickle cells Basophilic stippling Pappenheimer bodies Howell-Jolly bodies