• Urticaria isa vascular reaction of the skin
characterized by the appearance of
wheals and associated with severe itching,
stinging, or pricking sensations
3
2. Chronic urticaria:
Duration>6 weeks and continuous (occurs
at least 2x/week when off of treatment)
Associations with HLA-DR4 and HLA-DQ8,
H. pylori gastritis, and intestinal
strongyloidiasis
Triggers; 60% ordinary (autoimmune,
psedoallergic, infection-related, idiopathic),
35% physical, 5% vasculitic
5
6.
3. Episodic urticaria:
Duration>6 weeks but not continuous
4. Physical urticaria: induced by exogenous
physical stimulus; lesions occur within
minutes of provocation and generally
resolve <2 hours and are localized to the
stimulated area
Examples include dermatographism,
cholinergic, cold, heat, solar, pressure,
exercise-induced, vibratory, and aquagenic
urticaria
6
7.
Clinical features
• Multiplepruritic whealsof different sizes
erupt anywhere on the body and ten fade
within 2-24 hours without bruising; often
appears in evening or upon waking; most
intense at night
• In severe cases can be associated with
fatigue, lassitude, sweats, chills,
indigestion, arthralgias
7
epidemiology
• Occurs atany age
• More common in women: chronic urticaria,
dermatographism, cold urticaria
• More common in men: pressure urticaria
10
11.
pathogenesis
• Increased releaseof histamine from mast
cells situated around the capillaries
• Increased capillary permeability
• Other substances besides histamine may
cause vasodilation and capillary
permeability (serotonin, leukotrienes,
prostaglandins, proteases, and kinins)
11
12.
Etiologic factors
• Drugs(most frequent cause of acute
urticaria) e.g. penicillin, aspirin
• Food – e.g. chocolate, shellfish, nuts,
peanuts, tomatoes, strawberries, melons,
pork, cheese, garlic, onions, eggs, milk,
and spices
• Food additives – yeast, dyes
• Infections – URTI (streptococcal), H.
pylori, Hepatitis B and C, helminths
12
13.
• Emotional stress– severe emotional
stress may exacerbate urticaria
• Menthol – found in mentholated cigarettes,
candy and mints, cough syrup, aerosol
sprays, and topical medications
• Neoplasms – urticaria has been
associated with carcinomas and hodgkin
disease
13
14.
• Inhalants –grass pollens, house dust
mites, feathers, formaldehyde, soybean
dust, cottonseed, animal dander,
cosmetics, aerosols, etc
• Alcohol: alcohol-induced mast cell
stimulation
• Hormonal imbalance: urticaria twice as
common among women than men
14
15.
• Genetics: polymorphismsin the β2
adrenergic receptor gene have been
identified in aspirin-intolerant acute
urticaria
15
16.
diagnosis
• Usually madeon clinical grounds
• Lesions in a fixed location for more than
24h suggest the possibility of urticarial
vasculitis, urticarial phase of an
immunobullous eruption, EM, granuloma
annulare, sarcoidosis, or CTCL
• If individual wheals last for longer than
24hrs, a skin biopsy should be performed
16
17.
Treatment
• Antipruiritic lotionsand avoidance of
triggers
• First line: Antihistamines
• Second line: systemic corticosteroids
• Third line: immunotherapy (for severe
refractory autoimmune urticaria only);
IVIG, cyclosporine, plasmapheresis
17
• Angioedema isan acute, evanescent,
circumscribed edema that usually affects
the most distensible tissues, such as the
eyelids, lips, earlobes, and external
genitalia, or mucous membranes of the
mouth, tongue, or larynx
• The swelling occurs in the deeper parts of
the skin or in the subcutaneous tissues
and as a rule is only slightly tender, with
the overlying skin unaltered, edematous,
or, rarely ecchymotic 19
20.
• There maybe diffuse swelling on the
hands, forearms, feet, and ankles
• Frequently the condition begins during the
night and is found on awakening
20
pathogenesis
• Hereditary AE:mutation in structural gene
for C1 inhibitor leading to:
- reduced quantity (type 1)
- reduced function (type 2)
• Acquired AE: secondary to formation of
inhibitory autoantibodies against C1 INH
or persistent low-level activation of C1q
24
25.
Clinical features
• Canmerge with wheals, especially at eyelids
• Can be a feature of anaphylaxis if the throat is
involved
• Hereditary AE: low C4
• Acquired AE: low C4 and low C1q
• Vibratory AE: hereditary (AD) or acquired;
vibratory stimulus (jogging, motorcycles) lead to
localized swelling and erythema in minutes
• Food/exercise-induced anaphylaxis: occurs
within minutes of exercise after prior ingestion of
specific foods or within 4 hours of a heavy meal
25
26.
treatment
• As inurticaria
• For C1 esterase inhibitor deficiency
- Emergency: give C1 inhibitor concentrate
or FFP (life saving)
- Antihistamines, corticosteroids, and
epinephrine do not work
- Treatment of choice: anabolic steroids
(stanozolol or danazol)
26
Clinical features
• Consideredan urticarial dermatosis and
not urticaria
• Lesions last > 24 hrs (unlike urticaria)
although clinically appears like urticaria
• Lesions are pruritic and/or painful (burning
sensation)
• Often occurs at pressure points and may
resolve with residual purpura
29
30.
• 40% developangioedema; 50% develop
arthralgia
• Course is unpredictable
• Acute hemorrhagic edema of childhood:
urticarial vasculitis with prominent
cutaneous hemorrhage in young children
30
pathology
• Evidence ofleukocytoclastic vasculitis,
fibrinoid deposits in/around blood vessels,
extravasation of red cells, endothelial cell
swelling, perivenular cellular infiltrate rich
in neutrophils
• Need to biopsy a lesion that is < 24 hours
old for accuracy
32
33.
treatment
• No universallyeffective therapy
• Antihistamines are usually insufficient
except in mild cases
• 50% improve with NSAIDs
• Isolated positive reports with colchicine,
dapsone, hydroxychloroquine
33