Allergy and Immunology Flashcards

1
Q

Difference between anaphylaxis and anaphylactoid reaction

A

Anaphylaxis = IgE mediated with prior sensitization to the antigen

Anaphylactoid reaction = non-IgE related, clinically identical and treated the same way, but do not need preceding sensitization to the antigen

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2
Q

Best initial therapy for anaphylaxis

A
  1. Epinephrine
  2. Antihistamines: diphenhydramine (H1-blocker) and ranitidine (H2-blocker)
  3. Glucocorticoids
  4. Emergent airway protection if needed
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3
Q

Although angioedema is often idiopathic, what medication should you ask about in patients presenting with sudden swelling of their face/tongue/eyes/airway?

A

If they recently started an ACE inhibitor

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4
Q

True/False

Hereditary angioedema DOES NOT respond to glucocorticoids

A

True

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5
Q

Best initial test when suspecting angioedema

A

Decreased levels of C2 and C4

2/2 deficiency of C1 esterase inhibitor

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6
Q

Treatment for angioedema

A
  1. Protect the airway
  2. FFP or Ecallantide
  3. Androgens: danazol and stanazol
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7
Q

Define Urticaria

A

Allergic reaction that causes sudden swelling of the superficial layers of the skin (considered part of anaphylaxis)

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8
Q

Treatment for urticaria

A
  1. Antihistamines
  2. Leukotriene receptor antagonists
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9
Q

Treatment for allergic rhinitis

A
  1. Avoidance of allergen (e.g., cover mattresses and pillows)
  2. Intranasal corticosteroid sprays
  3. Antihistamines
  4. Intranasal anticholinergic medications
  5. Desensitization
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10
Q

Low B cell output

Normal T cells

A

CVID

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11
Q

Low B cells

Normal T cells

Young male

A

X-linked (Bruton) agammaglobulinemia

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12
Q

Low B cells and T cells

Analogous to HIV

A

SCID

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13
Q

Atopic disorders

Anaphylaxis

A

IgA deficiency

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14
Q

Recurrent skin infections with Staph

A

Hyper IgE syndrome

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15
Q

Normal T cells

Normal B cells

Low platelets

Eczema

A

Wiskott-Aldrich syndrome

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16
Q

Infections, combined with:

Staph

Burkholderia

Nocardia

Aspergillus

A

CGD

17
Q

Recurrent sinopulmonary infections in adults (equal gender distribution) with normal amounts of lymphoid tissue (nodes, adenoids, and tonsils)

A

CVID

Increased risk of lymphoma

Treatment = IVIG

18
Q

Absence of tonsils, adenoids, and lymph nodes

Male children with increased sinopulmonary infections

A

X-linked (Bruton) Agammaglobulinemia

Treatment = IVIG

19
Q

Treatment for SCID

A

Bone Marrow Transplant (BMT)

20
Q

Anaphylaxis to blood transfusion

A

Think IgA deficiency

21
Q

Should you give IVIG to someone with IgA deficiency

A

No

They will not work because the amount of IgA in the product is too insignificant to be therapeutic and the trace amounts of IgA in IVIG may provoke anaphylaxis

22
Q

Treatment for Hyper IgE Syndrome

A

Prophylactic antibiotics (dicloxacillin or cephalexin)

23
Q

Treatment for Wiskott-Aldrich Syndrome

A

BMT (T lymphocytes are markedly deficient in the blood and lymph nodes)

24
Q

Diagnostic test for CGD

A

Abnormal nitroblue tetrazolium testing

Detects decrease in the respiratory burst 2/2 a decrease in NADPH oxidase