Pictures Flashcards

1
Q
A

normal red blood cells

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2
Q
A

eosinophil

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3
Q
A

basophil

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4
Q
A

monocyte

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5
Q
A

lymphocyte

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6
Q
A

lymphocyte

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7
Q
A

reactive lymphocyte

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8
Q
A

large granular lymphocyte

(NK cell or cytotoxic T cell)

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9
Q
A

neutrophil

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10
Q
A

left shift: neutrophil variants

horseshoe nuclei: band

bean nuclei: metamyelocytes

round nuclei: myelocyte

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11
Q
A

neutrophil with toxic granulation

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12
Q
A

platelet

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13
Q
A

giant platelet

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14
Q

Describe RBC

A

normocytic, normochromic RBC

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15
Q

Describe RBC

A

hypochromic RBC

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16
Q

Describe RBC

A

Hypochromia, anisocytosis, poikilocytosis

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17
Q
A

polychromasia

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18
Q
A

sickle cell

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19
Q
A

Bite cells and hemoglobin clumps

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20
Q
A

schistocytes

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21
Q
A

blast

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22
Q
A

promyelocyte

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23
Q
A

myelocyte

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24
Q
A

metamyelocyte

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25
Q
A

band

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26
Q
A

pronormoblast

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27
Q
A

basophilic erythroblast

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28
Q
A

polychromatophilic

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29
Q
A

normochromic erythroblast

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30
Q
A

immature megakaryocyte

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31
Q
A

mature megakaryocyte

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32
Q
A

bone marrow core biopsy (5 year old)

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33
Q
A

bone marrow core biopsy (35 years old)

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34
Q
A

bone marrow core biopsy

top circle: erythroid

bottom circle: myeloid

arrow: megakaryoctye

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35
Q
A

normal bone marrow

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36
Q

Describe.

Name.

A
  1. microcytosis, hypochromia, anisocytosis, poikilocytosis
  2. Iron deficiency
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37
Q

Describe.

Name.

A
  1. microcytosis, hypochromia, target cells
  2. beta thalasemia
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38
Q

Describe.

Name.

A
  1. impaired nuclear maturation indicated by red nucleus, enhanced cytoplasm
  2. meagaloblastic RBCs
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39
Q

What is this and what causes it?

A
  1. megoblastic anemia
  2. impaired B12 uptake, folate deficiency, some drugs, bone marrow dysfunction
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40
Q

Describe.

Name.

A
  1. normocytic, iron
  2. anemia of chronic infection
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41
Q

Describe.

Name.

A
  1. spherocytes
  2. hereditary spherocytosis
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42
Q

Describe.

Name.

A
  1. hemoglobin crystals
  2. Hemoglobin C disease
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43
Q
A

polychromasia (increased reticulocytes)

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44
Q

Describe.

Name.

A
  1. heinz bodies
  2. G6PD deficiency
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45
Q
A
  1. cell that looks like it has a blister
  2. G6PD deficiency
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46
Q
  1. Left arrows
  2. Upper right arrows

What is this?

A
  1. merozoites
  2. gametocyte
  3. Plasmodium falciparum
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47
Q
A

Plasmodium vivax

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48
Q
A

babesia

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49
Q
A

Bartonella bacilliformis

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50
Q
A

Bartonella bacilliformis

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51
Q
A

C. perfringens

52
Q
A

Warm autoimmune hemolytic anemia

53
Q
A

Warm autoimmune hemolytic anemia

54
Q

Describe.

Name.

A
  1. red cell agglutination
  2. cold autoimmune hemolytic anemia
55
Q

Describe.

Name.

A
  1. schistocytes
  2. microangiopathic hemolytic anemia due to thrombotic thrombocytopenia purpura
56
Q
A

hypersegmented neurtrophil

megaloblastic anemia

57
Q
A

megaloblastic anemia

A and C: abnormally large erythroid progenitors

B: megaloblast

58
Q
A

Iron Deficiency

59
Q
A

hemochromatosis

60
Q
A

angular cheilosis: ulceration at corners of mouth

iron-deficiency

61
Q
A

koilonychia: spooning nails (concave, rigid, brittle)

iron-deficiency

62
Q
A

glossitis: bald fissured appearance caused by flattening and loss of papillae

Iron-deficiency

63
Q
A

iron deficiency:

hypochromic, microcytic, poikilocytes, pencil cells, occasional target cells, plenty of platelets

64
Q

Bone marrow: Perl’s stain

A

normal iron stores: blue

65
Q

Bone marrow: Perl’s stain

A

iron deficiency

no hemosiderin

inset: no siderotic granules in erythroblasts

66
Q
A

bronzing of skin: due to iron in melanin

hemachromatosis

67
Q
A

lots of iron in hepatocytes

hematochromatosis

68
Q
A

ring sideroblasts with perinuclear ring of iron granules

sideroblastic anemia

69
Q
A

lead poisoning

causes sideroblastic anemia

70
Q
A

basophilic stippling: precipitated RNA in RBC

71
Q
A

pallor and mild icterus

megaloblastic anemia

72
Q
A

Glossitis: beefy, red, painful

Megaloblastic anemia: folate deficiency and B12 deficiency

73
Q
A

Macrocytic RBC

74
Q
A

hypersegemented neutrophil

megaloblastic anemia

75
Q
A

Cracked Erythroblast: megaloblastic anemia

76
Q
A

demyelation of the lateral (pyrimidal) and posterior columns

B12 deficiency: severe neuropathy at this stage

77
Q
A

sickle cell anemia

78
Q
A

top: Spleen in sickle cell disease (low power). Red pulp cords and sinusoids are markedly congested; between the congested areas, pale areas of fibrosis resulting from ischemic damage are evident.
bottom: Under high power, splenic sinusoids are dilated and filled with sickled red cells.

79
Q
A

infarcted spleen due to sickle cell anemia

80
Q
A

Thalassemia. X-ray film of the skull showing new bone formation on the outer table, producing perpendicular radiations resembling a crewcut.

81
Q
A

facial abnormalities seen in beta thalassemia

bossing of skull, hypertrophy of maxilla, exposing upper teeth, depression of nasal bridge, periorbital puffiness

82
Q
A

Expanded marrow in Skull: Beta thalassemia

83
Q
A

osteoporosis: Beta thalassemia

84
Q
A

splayed teeth due to widening of the maxilla and mandible

Beta thalassemia

85
Q
A

Beta thalassemia

pallor, short, massive spleen, wasted limbs

86
Q
A

ulcer: can occur in all types of hereditary anemias including sickle cell, B-thalassemia, hereditary spherocytosis

87
Q
A

B-Thalassemia major

nucleated RBC, microcytosis, hypochromasia, target cells, teardrop cells, fragments, basophilic stippling

patient short of breath: look for heart failure due to iron load (freq. transfusions)

88
Q
A

thalassemia trait

microcytosis, hypochromasia, target cells, teardrop cells, rare fragments

low MCV/MCh and increased RDW helps distinguish from iron deficiency

89
Q
A

B-Thalassemia

fibrosis in portal tracts and nodular regeneration of hepatic parencymal cells, lots of iron

90
Q
A

B-Thalassemia with pre-existing hep Ccarcinoma on left, and hepatic cirrhosis on right

91
Q
A

hepatomegaly, heart failure, splenomegaly, edema, die

hydrops fetalis (gamma4)

92
Q
A

alpha-thalassemia: HbH

deposits: precipitated alpha globin chains and golf ball cells

93
Q
A

HbH

right: inclusion body (golfball with deposits-> beta tetramers)
left: reticulocyte

94
Q
A

HbH

microcytosis, hypochromasia, target cells, microspherocytes, fragments, some basophilic stippling may occur

95
Q
A

sickle cell anemia

deep stained sickle cells, target cells, polychromasia, hypochromic

96
Q
A

sickle cell anemia

left: dactylitis
right: leading to shortened fingers in adulthood

97
Q
A

sickle cell anemia

shortened finger due to dactylitis in childhood

98
Q
A

sickle cell anemia

right middle metacarpal bone shortened due to infarction of growing epiphysis in childhood

99
Q
A

pelvis necrosis, flattening of femoral heads

sickle cell anemia

100
Q
A

sickle cell anemia: chest syndrome

alveolar edema and fat cell embolism

101
Q
A

Sickle Cell/ hemoglobin C disease

102
Q
A

teleangiectasia: vascular malformations on face, lips and hands

can get in iron deficiency

103
Q
A

iron deficiency

smooth, shiny, red tongue and koilonychia (spoon nails)

104
Q
A

normal RBCs

105
Q
A

target cells

106
Q
A

acanthocytes: spur cells

107
Q
A

echinocytes: burr cells

108
Q
A

dacrocytes: tear drops

109
Q
A

spherocytes

110
Q
A

ovalocytes

111
Q
A

blister cells at arrows

112
Q
A

bite cells

113
Q
A

schistocytes

114
Q
A

sickle cells

115
Q
A

dehydration effect of RBC

116
Q
A

Howell-Jolly bodies

117
Q
A

nucleated RBC precursors

118
Q
A

pappenheimer bodies

119
Q
A

trophozoites of Plasmodium vivax

120
Q
A

coarse basophilic stippling of lead poisoning

121
Q
A

heinz bodies in person with spleen removed

122
Q
A

B12 deficiency

giant hypersegemented neutrophil

123
Q
A

hypersegmented neutrophils from antifolate chemo

124
Q
A

myelodysplastic syndrome

dysplastic neutrophil (pseudopelgeroid cell)

125
Q
A

degenerating neutrophil