Allergy Flashcards
(37 cards)
Anaphylaxis, type and etiology?
Type 1
IgE to mast cells
Degranulation
Vasodilation
Anaphylaxis, presentation
Low BP Fast or slow HR Hives, prurits angiodema headache, vomiting diarrhea, SOB, cough
Autoimmune hemolytic anemia, type and etiology?
Type 2, cytotoxic
IgG bind to RBCs, leading to premature destruction,
-1/2 cases idiopathic
Autoimmune hemolyic anemia, presentation?
Symptoms - non specific, may have general symptoms of anemia -fatigue etc.
- jaundice or splenomegaly
- reticulocytes in peripheral blood smear
Poststreptococcal glomerulonephritis, type and etiology?
Type 3, Immune complex mediated
- prior infection of beta hemolytic strep
- immune complexes form and get stuck in glomeruli
Contact Dermatitis, type?
Type 4, Delayed Hype reaction
PSGN background info?
History of pharyngitis summer
-or impetigo in winter
Contact dermatitis, etiology?
Phase 1- sensitization
Phase 2- Allergic response after preexposure.
May take months or years to see response
Contact dermatitis, symtoms?
Primary= intense pruritis
Pain with excoriation, risk of secondary infection
-transient erythema, vesiculation, swelling with bullae
Serum sickness, type and etiology?
Type 3, ICF
admin of nonhuman protein leads to AB response
- ICF deposits in small vessels/tissues = vasculitis and tissue injury
Ex. antitoxins and antivenims
Vasculitis, type and etiology?
Type 3, ICF
Immune complexes get stuck in vessel walls.
Three types of vasculitis?
Small- Henochschonlein purpurn
Medium - Kawasaki disease
Large vessel - Giant cell(temporal) arteritis
Symptoms of vasculitis?
Regardless of size, systemic inflammation:
- fever, night sweats
- fatigue, anorexia, weight loss
- arthralgias, arthritis
SMall= thick palpable purpura
Transplant rejection, type and etiology?
Type 4, delayed
Graft destruction caused by T cell-mediated to allograft histocompatibility antignes
Transplant rejection, symptoms
Broad: fevers, chills, malaise, arthralgias
Anaphylaxis vs. anaphylactoid?
Anaphylaxis = IgE dependent
Anaphylactoid = IgE independent
- no sensitization required
- can occur on first exposure
- not predicted by skin test
Urticaria
Hives
Swelling of upper dermis
rasied blebs (wheals) with circuscribed edges (red halo)
Itching (pruritis)
Angioedema -acquired
swelling of the deep dermis
characterized by pain or burning not pruritus
-typically affects the face
Angioedema - hereditary
deficiency of complement inhibitors
leads to recurrent potentially life threatening attacks facial, laryngeal and GI swelling
Urticaria and angiodema pathphys, and Treatment?
-Type 1 hypersensitivity, degranulation of mast cells
Histamine binds to H1 and H2, causing aterial dilation, venous constriction, increased capillary permeability
Treatment: ovar H1 antihistamine
Atopic diseases
- allergic rhinitis
- atopic dermatitis
- allergic asthma
- allergic gastroenteropathy
Food allergy vs. food intolerance?
allergy = specific immune response
-potentially life threatening
intolerance = associated with digestion
- not life threatening
Most common food allergies?
IgE associated:
- milk, eggs, peanut, soy, wheat, tree nuts, fish, shellfish
- asthma and urticaria not likely to be caused by food allergies
exanthematous/
morbilliform
Etiology: commonly penicillin family
S&S: “rash all over,” widespread symmetric, erythematous macules and papules on the trunk and extremities, pruritus, mild, fever
-First exposure rash after 7-10 days
Most common of all cutaneous drug eruptions (90%)
- Stop medication, resolves a few days to a week after the medication is stopped, can continue medication if not too severe and meds can’t be substituted, resolves without sequelae
- Treat: topical steriods and oral antihistamines