10 - Benign Leukocyte Disorders Flashcards

1
Q

eosinophil protein that gives it eosinophilia

A

major basic protein

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2
Q

normal differential of WBCs

A
neutrophil - 55%
lymphs - 35%
monos - 6%
eos - 3%
basos - 1%
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3
Q

leukemoid reaction

A

reactive inc in WBC count, usually refers to granulocytes

immature forms may appear in peripheral blood

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4
Q

causes of neutrophilia

A

reactive:
infections (bacterial)
inflammation/necrosis
drugs, hormones, toxins (steroids, Cushings)
strong physical/emotional stimuli / trauma

neoplastic: myeloproliferative neoplasms

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5
Q

causes of eosinophilia

A
reactive:
infxn (parasite, fungal)
allergy
drugs
collagen vascular dz
addison's dz

neoplastic:
myeloproliferative neoplasms
some T cell lymphomas/leukemias

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6
Q

causes of basophilia

A

rare - usually myeloproliferative neoplasm like CML

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7
Q

causes of monocytosis

A
reactive - 
neutropenia
collagen vascular dz
immune disorders
infxns (viral, tb, syph, bact endocarditis

neoplastic -
myeloproliferative neoplasms and leukemias

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8
Q

causes of lymphocytosis

A
reactive:
infxns (viral, pertussis, TB, rickettsia)
infectious mononucleosis
autoimmune
drugs

neoplastic - lymphomas/leukemias

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9
Q

when does the absolute neutrophil count become alarmingly low

A

<500 is REALLY bad

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10
Q

consequences of neutropenia

A

inc risk of bacterial/fungal infection (more of a problem with acute drops than chronic process)
ulcerations of oral cavity, skin, GI, GU
sx related to infxn - fever, chills, malaise

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11
Q

causes of neutropenia

A
inherited - congenital, cyclic
reactive-
nutritional deficiencies
drugs
severe infxn
autoimmune
neoplastic: 
acute leukemia
MDS
large granular lymphocyte leukemia
tumor in bone marrow
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12
Q

Kostmann syndrome

A

rare AR disorder

causes agranulocytosis due to mutation in elastase

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13
Q

causes of monocytopenia

A

aplastic anemia

hairy cell leukemia

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14
Q

causes of lymphopenia

A
HIV
immune deficiency
infxns
drugs (immunosuppressants)
autoimmune dz
malnutrition
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15
Q

dohle bodies - what are they

A

round/oval/rod pale gray/blue inclusions in neutrophil

stacks of RER or denatured aggregates of free ribosomes

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16
Q

when do you see dohle bodies?

A
normal pregnancy
infxn
various neoplasms
severe burns
trauma
G-CSF therapy
kwashiorkor
17
Q

toxic granulation - what is it

A

fine coarse reddish granules in neutrophil

result from altered maturation of granules

18
Q

when do you see toxic granulation

A
severe infxn
other inflammatory states
pregnancy
trauma
burns
G-CSF therapy
19
Q

when do you see vacuoles in cytoplasm of neutrophils?

A
septicemia
acute alcohol poisoning
carnitine deficiency
kwashiorkor
*may be artifact of sample hanging out in EDTA too long
20
Q

Pelger Huet anomaly

A

AD inheritance
hyposegmentation of neutrophil
function is normal usually

21
Q

when do you see hyposegmentation of neutrophils?

A
inherited - Pelger Huet anomaly
acquired - myelodysplasia and AML
drugs
infxn (mycoplasma, HIV)
rarely in bone marrow transplant pts
22
Q

when do you see hypersegmentation of neutrophils?

A

most common - megaloblastic myelopoiesis
B12 or folate deficiency
alcoholism
drugs

23
Q

chronic granulomatous disease

A

rare X linked disorder
defective oxidative burst - cant make H2O2, so catalase pos organisms cant be killed > make granulomas > recurrent abscesses, infections

24
Q

May Hegglin anomaly

A

AD inheritance
intracytoplasmic inclusions in granulocytes and monocytes (looks like a basophilic shadow)
giant platelets

25
Q

Chediak Higashi Syndrome

A

AR inheritance
reduced and abnormally large granules - look very unique
partial oculocutaneous albinism
recurrent infections

26
Q

Alder Reilly anomaly

A

AR inheritance
seen in mucopolysaccharidoses
abnormally coarse azurophilic granules in neutrophils and sometimes lymphs and monos