Allergy/Immunology Flashcards
0
Q
Antibody mediated allergic response
A
Type II Allergic Reaction
1
Q
IgE mediated (anaphylactic) allergic reaction
A
Type I Allergic Response
2
Q
Immune Complex Deposition
A
Type III Allergic Reaction
3
Q
Delayed Hypersensitivity (Poison Ivy) Reaction
A
Type IV Allergic Reaction
4
Q
Recurrent pyogenic infections
A
B cell (Ab) dysfunction
5
Q
Chronic or recurrent candida infection (nails, scalp, or mouth)
A
T cell dysfunction
6
Q
- Eczema and petichiae (thrombocytopenia)
- X-linked
- low IgM
- humoral and cellular immunodeficiency
- autoimmune disease and malignancy
- Tx: manage bleeding and infx, BMT
A
Wiskott Aldrich Syndrome
7
Q
- absence of lymphoid tissue
- defect in B and T cell function
- dermatitis, diarrhea, FTT, thrush, otitis, LTI
- low normal WBC
- Dx: analysis of T, B, and NK cell subsets
- Tx: BMT
- also adenosine deaminase deficincy
A
SCID
8
Q
-absence of thymic shadow Cardiac defects Abnl face (low set ears) Thymic hypoplasia Cleft palate Hypocalcemia (tetany) 22- long arm of Xsome 22
A
DiGeorge Syndrome
9
Q
- “ataxia” w/ discoloration of the conjunctiva
- frequent sinus infx
A
Ataxia Telangectasia
10
Q
- No B cells
- decr lymphoid tissue
- recurrent infx with encapsulated pyogenic bacteria (pseudomonas, S. pneumo, H. flu)- pna, otitis
- X-linked
- low IgGAMEs–>B&T cell subsets
- require IVIG
A
Bruton’s X-linked agammaglobulinemia
11
Q
- defective Ab response
- B lymphocytes don’t differentiate
- deficiency of Ig sub-types
- may have T cell defects too
- recurrent URTI, LRTI, herpes zoster
- associated with autoimmune disease, lymphoma and EBV
- require IVIG
A
CVID
12
Q
- recurrent overwhelming meningococcal disease
- most are autosomal recessive
A
Complement deficiency
13
Q
- T cell abnl prevents IgM–>IgG
- absence of CD 40 ligand
- disruption of B cell differentiation
- frequent otitis, sinopulmonary infx, diarrhea, and opportunistic infx
- low IgG, A, E, incr IgM
- X linked (males)
- Tx: IVIG
A
Hyper IgM
14
Q
- MC immunodeficiency
- recurrent sinopulmonary infx
A
IgA deficiency