Peripheral Blood Smears Flashcards

1
Q

Anisocytosis

A

unequal sized RBCs

cellar are are otherwise uniform

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2
Q

Microcytosis

A
Iron deficiency anemia
Thalassemia
Anemia of chronic disease
Sideroblastic anemias
Chronic lead exposure
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3
Q

Macrocytosis

A

Folate/B12 deficiency
Liver disease
Primary bone marrow failure; myelodysplasia
Reticulocytosis (polychromasia)

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4
Q

Hypersegmented neutrophils

A

normally should have 4-6 lobes
these have 9-9 lobes and are larger
seen in megaloblastic anemia

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5
Q

Poikilocytosis

A

indicates the shape of thecells

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6
Q

macroocalocytes

A

large oval cells

B12/foltae megaloblastic anemia

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7
Q

Eliiptocytes

A

heriditary,

ellipsoid

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8
Q

Fragmetned erythrocytoses

A

chopped up RBCs (aka schistocytosis)
TTP, DIC, HUS
**prosthetic heart valves
hemolytic anemisa

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9
Q

acanthocyte

A

(Burr cell)
RBC w/ irregular shaped cells
liver disorders

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10
Q

Codocyte

A

aka target cells

red cells w/ central color spot in area of pallor (SCA, HbC, thalassemias)

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11
Q

dacrocyte

A

teardrop
myeloproliferative disorders
pernicious anemia
thalassemias

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12
Q

Stomatocyte

A

folded RBC mimicking a mouth and lips (slit-like appearance)
seen in hemolytic anemias
constitutive or acquired

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13
Q

Hypochromia

A

increased pallor int he center of RBC, lack of Hb
Thalassemia
Iron deficiency anemia
Sideroblastic anemia

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14
Q

Normochromic

A

normal Hb and stain w/ normal RBC intensity on peripheral smears
central pallor is 1/3 of cell

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15
Q

Hyperchromic

A

DOES NOT EXIST

can only cram 270mil Hb into 1 RBC

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16
Q

Rouleaux

A

stack of coins

seen in MM d/t elevated plasma globulins or globulins

17
Q

Clumping

A

d/t cold agglutinins

18
Q

basophilic stippling

A

round dark blue granules in retics on smears stained

classic lead poisoning

19
Q

Reticulocytes

A

): immature red cell progenitors not normally present in blood
The nucleus is pyknotic
undergoing hemolytic crises.(normal in new-borns)

20
Q

Howell Jolly Bodies

A

Spherical blue-black red cell inclusions seen on Wright-stained smears.
nuclear fragments,
hemolytic anemias and in post-splenectomy patients (below).

21
Q

Signet ring

A

indicates infection by plasmodium vivax

22
Q

Neutrophilia

A

elevated in bacterial infections, stress, corticosteroids

immature forms often present w/ elevated count

23
Q

Lymphcytosis

A

elevated in viral infections

“atypical lymphocytes”= EBV mono

24
Q

fragile lymphocytes

A

smudge or basket cells

common in CLL

25
Q

Basophilia

A

elevated in CML

26
Q

Left shift

A

indicates more immature forms of PMNs

d/t increased production (infection, myeloid cancers)

27
Q

Dohle body

A

toxic granulations w/in PMN made of cytoplasmic vacuoles
indicates infections

often w/ L shift

28
Q

Reduced lobulation of PMN

A

often associated w/ myelodysplastic syndromes

29
Q

Giant Plt

A

Suggest marrow response secondary to increased platelet destruction or consumption

Congenital disorders
Immune destruction
Disseminated intravascular coagulation (DIC)
Hemolytic uremic syndrome (HUS)
Thrombotic thrombocytopenic purpura (TTP)

30
Q

normoblasts

A

immature red cell progenitors not normally present in blood.
pyknotic nuclei
patients undergoing hemolytic crises.