Anemias Flashcards

1
Q

Neutrophilia Causes

A

Bacterial infection (most common)
Some viral and fungal infections
Chronic Inflammation
Smoking, exercise, stress

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2
Q

Leukemoid Reaction vs. CML

A

Leukemoid Reaction: WBC <50, left shift, normal RBC, normal platelets, LAP increased, philadelphia chromosome absent

CML: WBC >50, left shift, low RBC, varying platelets, LAP decreased, philadelphia chromosome present

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3
Q

Neutropenia

Range, conditions

A

Absolute neutrophil count <1.5 x 10^3/uL

Decreased bone marrow production: aplastic anemia
Increased cell loss: anemia, chemotherapy

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4
Q

Pelger Huet Causes

A

Leukemia or myelodysplastic syndromes

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5
Q

Hypersegmented Neutrophils

causes

A

Megaloblastic anemia, B12, folate deficiency

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6
Q

Dohle Bodies

A

Severe infections, burns, cancer, toxic drugs

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7
Q

Toxic Granulation

A

Bacterial infections

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8
Q

Alder-Reilly

A

Normal function, large granules

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9
Q

Chediak-Higashi

Symptom, diff, inclusions

A

Early death, recurrent infections, neutropenia, thrombocytopenia, blue-green bodies

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10
Q

May-Hegglin

Inclusions? Smear?

A

Inclusions that look like Dohle bodies
Giant platelets, low platelet count, bleeding

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11
Q

Chronic Granulomatous Disease

A

Respiratory burst oxidase system, cannot generate oxygen to kill microorganisms

Form granulomas around pathogens in tissue

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12
Q

Reticulocytes

What are they, stain qualities,

A

Immature red blood cells with increased RNA
On wright stain, polychromatophilic cells
On new methylene blue supravital stain, blue granules

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13
Q

Reticulocyte Smear Procedure

A

1:1 ratio of blood to new methylene blue
Incubate for 15 minutes at room temperature in the stain

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14
Q

Miller Disc Formula

A

% retic = (# retics counted x 100) / (# RBCs counted x 9)

Count at least 112 RBCs, should have 5-7 RBCs in little square

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15
Q

RPI and Corrections

If pt HCT <45%

A

(% retic count / maturation time) x (patient HCT/45)

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16
Q

RPI Interpretation

A

<2.0: decreased production, Fe deficiency, aplastic anemia
>2.0: increased destruction, hemolytic anemia

16
Q

Absolute Retic Count Formula

A

(% retic x RBC should be given) / 100

16
Q

Sickle Cell Trait vs. Disease

Which is worse?

A

Sickle cell trait has one copy of mutation, not as many symptoms unless under low oxygen tension

16
Q

High Pressure Liquid Chromatography (HPLC)

What does it do, patient population

A

Separates and quantifies hemoglobin

Newborn screening

Done before electrophoresis

17
Q

Sickle Quick

Screens for, procedure, interpret, bad for

A

Screens SS disease and AS trait

RBCs lysed and hgb released, HgS is insoluble, will form turbid suspension in phosphate buffer

False positive in HbC Harlem or low hemoglobin

Bad test for babies, false negative from HgF

18
Q

Electrophoresis

What does it do, order for alkaline and acid, traveling trends

A

Identifies hemoglobin proteins based on electrical charges

Alkaline: CSFA
CEO, SDG travel together
H and Barts faster than A (won’t show up)

Acid Citrate: FASC
ADGEO travel together