Allergy/Immuno Flashcards

(59 cards)

1
Q

triggers for vasomotor rhinitis

A

cold air, tearing, pollution and emotion

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2
Q

gold standard of dx food allergy is

A

oral food test in front of cliniciNS

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3
Q

what kind of allergy testing isnt affected by recent antihistamine use

A

RAST since is a blood test measuring for IgE

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4
Q

C1 esterase deficiency causes whst

A

hereditary angioedema

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5
Q

what medicine blunts the effects of epinephrine and should be reversed if the patient is having anaphyaxis and needs epi

A

beta blocker, give glucagon to reverse

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6
Q

what formula should you use for milk protein allergy

A

hydrolyzed not SOY

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7
Q

is FPIES IgE mediated

A

no

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8
Q

when does FPIES get better

A

as the GI tract matures

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9
Q

Bloody diarrhea or reg diarrhea and emesis in a patient drinking cows formula but not when on clears and eating foods with none whole protein contents , dx?

A

FPIES

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10
Q

what is food protein induced enterocolitis syndrome

A

a severe reaction to an allergen about 1-3 hours after ingestion, severe vomiting and diarrhea (cows milk and soy are culprits)

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11
Q

hydrogen breath test tests for what

A

lactase deficiency

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12
Q

type 3 HS reaction is?

A

immune complex

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13
Q

ype 4 HS reaction is

A

cell mediated ( t cell) “poison ivy”

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14
Q

type 2 HS reaction is

A

antibody mediated “ b cell”

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15
Q

type 1 HS reaxtion is

A

IGE mediated anaphylaxis

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16
Q

what medication blunts the response to epi? what should you give

A

beta blokers, give glucagon to reverse the effects

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17
Q

anaphylactoid reactions happen in reponse to whatr

A

contrast, PCN, vanc, NSAID and opitates

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18
Q

what should be given to prevent an anaphyactoid reaction

A

diphenhydramine and steroids

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19
Q

nephritis, arthralgias, arthritis and or rash after exposure to medication 1-2 weeks prior is known as

A

serum sickness

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20
Q

bee sting reactions are due to what

A

IgE mediated (type 2 HS rxn)

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21
Q

bee sting reactions are due to what

A

IgE mediated (type 2 HS helper t cells rxn)

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22
Q

bee sting reactions are due to what

A

IgE mediated (type 2 HS rxn)

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23
Q

helper t cells

A

CD4

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24
Q

Cytotoxic t cells

25
PJP is found in SCID and HyperIgM but not in
Bruton Agammaglobulinemia
26
chronic or recurrent fungal infections is seen in what kind of condition
t cell/ combined t cell deficiencies
27
skin testing like ppd check for what kind of HS rexn
Type 4
28
SCID is what kind of cell deficiency
t AND b cells " thats why it is called combined"
29
first 3–6 months with otitis media (OM), thrush, diarrhea, and dermatitis.
SCID
30
what is the cure for SCID
BMT
31
what should SCID patient's not receive
live vaccines
32
what are two common combined t and b cell deficiences
wiskott aldrich and SCID
33
lymphopenia is usually in relaiton to what cell line being low
t cells
34
what imunoglobulin is increased in WIA
IgA, IgM is dereased
35
what test is used to dx digeorge
FISH
36
what is an AR condition that involves the ineffective repaire of damaged DNA
ataxia telengeictasia
37
1st sig of ataxia telengiectasia
cerebellar ataxia around age 1
38
ataxia telengiectasia has an increased risk of malginancy when
in the 3rd decade of life
39
ataxia telengiectasia has what kind of recurring illness
pneumonia and sinusitis (AFP is high)
40
in what condition do B cells fail to form into plasma cells causing a deficiency of all the Ig subtypes
combined variable immunodeficiency
41
a risk of EBV associated lymphoma is seen in
CVID
42
recurrent HSV and VZV infections are common in
CVID
43
IgM will not class switch to IgG due to a missing signal from t and b cells in what syndrome
HyperIgM Syndrome
44
patients with HyperIgM syndrome have wat kind of infections
PNA, sinusitis and OM
45
tx for hyperIgM is
IVIG
46
how to test for b cell deficiency
obtain titers
47
condition where there are no b cells so no immunoglobulins
x linked agammaglobulinemia
48
when you see b cell, think of what kind of infection
bacterial
49
ch50 is a great test to tell between XLA agammaglbulinemia and C1-C4 esterase deficiency how?
CH50 is nl in XLA and low in C1-C4 complement deficiency
50
this condition: - presents at 6 month - only in boys - recurrent bacterial infections (encapsulated) - lack of B cells ( aka no Ig's ) - High T cells
X linked agammaglobulinemia
51
tx for XLA
IVIG, abx ppx or BMT is curative
52
transient hypogammaglobulinemia of infance has low what
IgG and IgA, gets better by age 3-6
53
eosinophils high, eczema and high IgEis
Hyper IgE syndrome
54
delayed shedding of primary dentition is seen in
Hyper IgE
55
impaired neutrophil chemotaxisi ( aka no erythema at infection sites) is seen in what condition
Hyper IgE
56
which complement deficiency is related to herditary angioededma
C1 esterase deficiency
57
neutropenia, oculocutaneous albinism, low platelets and recurrent indection with staff, what is the confition
chedik higashi syndrome
58
pancreatic insufficiecny + pancytopneia
schwachman diamond syndrome
59
pure red cell aplpasia (only red cell line affected) + triphalngeal thumb+macrocytosis
diamond blacfan anemia