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
Basophilia
elevated in CML
26
Left shift
indicates more immature forms of PMNs | d/t increased production (infection, myeloid cancers)
27
Dohle body
toxic granulations w/in PMN made of cytoplasmic vacuoles indicates infections often w/ L shift
28
Reduced lobulation of PMN
often associated w/ myelodysplastic syndromes
29
Giant Plt
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
normoblasts
immature red cell progenitors not normally present in blood. pyknotic nuclei patients undergoing hemolytic crises.