URTICARIA, EM &
DRUG ERUPTIONS
URTICARIA
• WHEALS
---------- transient <24hrs
superficial,
well demarcated
--------- erythematous/pale swellings of dermis
with itching
ANGIOEDEMA / QUINCKE’S
EDEMA
-poorly defined -affects deeper
dermal,s/c,submucosal
-pale/normal colour -usually last longer
-painful
CLASSIFICATION
• BASED ON DURATION
A/C ,C/C , episodic
CLASSIFICATION
• BASED ON CLINICAL PICTURE
-ordinary-a/c ,c/c
-physical&cholinergic -urticarial vasculitis
-contact urticaria -angioedema
without wheals
ACUTE URTICARIA
• CAUSES -IDIOPATHIC
-ALLERGIC
drug(penicillin), food(eg.shellfish), sting(eg.bee)
-NON ALLERGIC histamine
liberators -vanco pseudo allergic-
NSAIDS, pineapple -
INFECTION
CHRONIC URTICARIA
• PROVOKING/AGGRAVATING FACTORS -
drugs -food & food
additives -infection /
infestation -inhalants
-systemic d/s -implants
-menstrual cycle & pregnancy -stress
AUTOIMMUNE URTICARIA
• Due autoantibodies against FC€R1 receptors or to IgE bound
to the same receptor
• Lead to cross linking of 2 adjacent FC€R1 receptors and mast
cell degranulation
PHYSICAL URTICARIA
• DERMOGRAPHISM
• DELAYED PRESSURE URTICARIA
• CHOLINERGIC URTICARIA
• COLD URTICARIA
• SOLAR URTICARIA
• AQUAGENIC URTICARIA
URTICARIAL VASCULITIS
• >24-48hrs
• Burn/itch
• Tender/painful
• Residual bruising / staining
• Pupuric spots / rarely bullae
• Constitutional sympyoms
CONTACT URTICARIA
• ALLERGIC allergen
penetrate (eg.oral allergy syn)
• NON ALLERGIC by
direct injection of vasoactive chemicals by plants(eg.nettles)
or animals(eg.caterpillars)
Treatment of urticaria
• Antihistamines-H1 ,H2
• Steroids -a/c exacerbation
-UV -severe DPU
• Epinephrine-AE
• Plasmapheresis,IVIg, cyclosporine
HEREDITARY ANGIOEDEMA
• AD
• C1 esterase inhibitor deficiency
• Type1,2,3
• C4 screening, C1 esterase functional assay
• Rx-attenuated androgens,FFP, partly purified prep.n
ERYTHEMA MULTIFORME
• young age
• Mainly by infecton & drugs
• MCC- herpes simplex infection
• Extremities & face
• Mucosa may be involved
• Subsides in few weeks
• Typical lesion- target lesion
Target / iris lesion
• 3 ZONES
CENTRAL- dusky violaceous
erythema/blister/necrosis
MIDDLE- pale edematous
OUTER-erythema
treatment
• Symptomatic
• Systemic steroids if severe
• Acyclovir if recurrent
SJS TEN SPECTRUM
• SJS BSA<10%, 2 or
mucosa involved
• SJS-TEN OVERLAP BSA 10-
30%
• TEN BSA>30%
Drugs causing
• SHORT TERM -
penicillin,sulpha,quinolones,
cephalosporin ,p.mol
LONG TERM
-anticonvulsants,ATT,ART, allopurinol
SJS
• Sudden onset
• Prodrome
• Skin- erosions/blisters OR
EM like lesions
• Mucosa –oral(100%), eye(91%), genital(57%)
TEN
• SKIN -poorly
defined macules with purpuric/blistering centres
-EM like maculopapular rash
-confluent erythema -blisters over
palms&soles
• Extensive mucosal lesions
• Nikolsky +ve
Immediate Rx
• Withdrawal of offending drug
• Fluid replacement
• Nutritional support
• Dressing
• Temp regulation
• Corticosteroids,IVIg, cyclosporine
Continuing management
• Ophthalmic / oral care
• Antibiotics
• Monitoring of complications
• Prevention of recurrences
Prognosis-SCORTEN index
-age>40 -HR>120
-BUN>28mg/dl -RBS>252mg/dl
-HCO3- <20mg/ml
-initial BSA>30%
-presence of malignancy
1-3.2% 5or>5-90%
FDE
• Recurs at same site
• After 30mts-8hr
• Round/oval, sharply demarcated,itchy lesion
• Erythema&edema…..dusky violaceous
brown…..crusting&scaling………….post inflammatory
hyperpigmentation
• Limbs,hands&feet
• Oral,anal&genital
• Repeated attacks-new lesions,lesions increase in size
• Cotrimoxazole,tetracycline, NSAIDS
EXANTHEMATIC DRUG
ERUPTION
• Most common
• Upto 3 weeks
• Erosive stomatitis
• Face&pressure areas spared
• Intertriginous areas favoured
• Palmar&plantar lesions
• Purpuric lesions
• Penicillin,sulpha,NSAIDS, anticonvulsant
DHS
• DRESS / DIDMOHS
• After 3-6 weeks
• Facial edema with infiltrated papules
• Exnthematous rash …..exfoliative dermatitis
• Hepatitis,nephritis,pneumonitis,myocarditis
• Hypereosinophilia&atypical lymphocytes
• LNE
• DRUGS-anticonvulsants,sulpha, dapsone,minocycline,
terbinafine
• Rx- steroids
Drug induced pseudolymphoma
syndrome
• More insidious onset – usually after 7 weeks
• Facial edema+ but no fever
• Ery. plaques / multiple infiltrative papules
/ solitary nodule
• Rx- drug withdrawal
• Anticonvulsants,antipsychotics,antihistamines,CCB,ACEI,beta blocker
AGEP
• Multiple pustules with fever mimicking pustular psoriasis
• within 24 hrs
• Start on face& flexures
• penicillin / macrolide
Urticaria and drug eruptions

Urticaria and drug eruptions

  • 1.
  • 4.
    URTICARIA • WHEALS ---------- transient<24hrs superficial, well demarcated --------- erythematous/pale swellings of dermis with itching
  • 6.
    ANGIOEDEMA / QUINCKE’S EDEMA -poorlydefined -affects deeper dermal,s/c,submucosal -pale/normal colour -usually last longer -painful
  • 7.
    CLASSIFICATION • BASED ONDURATION A/C ,C/C , episodic
  • 8.
    CLASSIFICATION • BASED ONCLINICAL PICTURE -ordinary-a/c ,c/c -physical&cholinergic -urticarial vasculitis -contact urticaria -angioedema without wheals
  • 9.
    ACUTE URTICARIA • CAUSES-IDIOPATHIC -ALLERGIC drug(penicillin), food(eg.shellfish), sting(eg.bee) -NON ALLERGIC histamine liberators -vanco pseudo allergic- NSAIDS, pineapple - INFECTION
  • 10.
    CHRONIC URTICARIA • PROVOKING/AGGRAVATINGFACTORS - drugs -food & food additives -infection / infestation -inhalants -systemic d/s -implants -menstrual cycle & pregnancy -stress
  • 11.
    AUTOIMMUNE URTICARIA • Dueautoantibodies against FC€R1 receptors or to IgE bound to the same receptor • Lead to cross linking of 2 adjacent FC€R1 receptors and mast cell degranulation
  • 13.
    PHYSICAL URTICARIA • DERMOGRAPHISM •DELAYED PRESSURE URTICARIA • CHOLINERGIC URTICARIA • COLD URTICARIA • SOLAR URTICARIA • AQUAGENIC URTICARIA
  • 14.
    URTICARIAL VASCULITIS • >24-48hrs •Burn/itch • Tender/painful • Residual bruising / staining • Pupuric spots / rarely bullae • Constitutional sympyoms
  • 15.
    CONTACT URTICARIA • ALLERGICallergen penetrate (eg.oral allergy syn) • NON ALLERGIC by direct injection of vasoactive chemicals by plants(eg.nettles) or animals(eg.caterpillars)
  • 16.
    Treatment of urticaria •Antihistamines-H1 ,H2 • Steroids -a/c exacerbation -UV -severe DPU • Epinephrine-AE • Plasmapheresis,IVIg, cyclosporine
  • 17.
    HEREDITARY ANGIOEDEMA • AD •C1 esterase inhibitor deficiency • Type1,2,3 • C4 screening, C1 esterase functional assay • Rx-attenuated androgens,FFP, partly purified prep.n
  • 18.
    ERYTHEMA MULTIFORME • youngage • Mainly by infecton & drugs • MCC- herpes simplex infection • Extremities & face • Mucosa may be involved • Subsides in few weeks • Typical lesion- target lesion
  • 22.
    Target / irislesion • 3 ZONES CENTRAL- dusky violaceous erythema/blister/necrosis MIDDLE- pale edematous OUTER-erythema
  • 23.
    treatment • Symptomatic • Systemicsteroids if severe • Acyclovir if recurrent
  • 24.
    SJS TEN SPECTRUM •SJS BSA<10%, 2 or mucosa involved • SJS-TEN OVERLAP BSA 10- 30% • TEN BSA>30%
  • 25.
    Drugs causing • SHORTTERM - penicillin,sulpha,quinolones, cephalosporin ,p.mol LONG TERM -anticonvulsants,ATT,ART, allopurinol
  • 28.
    SJS • Sudden onset •Prodrome • Skin- erosions/blisters OR EM like lesions • Mucosa –oral(100%), eye(91%), genital(57%)
  • 31.
    TEN • SKIN -poorly definedmacules with purpuric/blistering centres -EM like maculopapular rash -confluent erythema -blisters over palms&soles • Extensive mucosal lesions • Nikolsky +ve
  • 32.
    Immediate Rx • Withdrawalof offending drug • Fluid replacement • Nutritional support • Dressing • Temp regulation • Corticosteroids,IVIg, cyclosporine
  • 33.
    Continuing management • Ophthalmic/ oral care • Antibiotics • Monitoring of complications • Prevention of recurrences
  • 34.
    Prognosis-SCORTEN index -age>40 -HR>120 -BUN>28mg/dl-RBS>252mg/dl -HCO3- <20mg/ml -initial BSA>30% -presence of malignancy 1-3.2% 5or>5-90%
  • 36.
    FDE • Recurs atsame site • After 30mts-8hr • Round/oval, sharply demarcated,itchy lesion • Erythema&edema…..dusky violaceous brown…..crusting&scaling………….post inflammatory hyperpigmentation
  • 38.
    • Limbs,hands&feet • Oral,anal&genital •Repeated attacks-new lesions,lesions increase in size • Cotrimoxazole,tetracycline, NSAIDS
  • 40.
    EXANTHEMATIC DRUG ERUPTION • Mostcommon • Upto 3 weeks • Erosive stomatitis • Face&pressure areas spared • Intertriginous areas favoured • Palmar&plantar lesions • Purpuric lesions • Penicillin,sulpha,NSAIDS, anticonvulsant
  • 41.
    DHS • DRESS /DIDMOHS • After 3-6 weeks • Facial edema with infiltrated papules • Exnthematous rash …..exfoliative dermatitis • Hepatitis,nephritis,pneumonitis,myocarditis
  • 42.
    • Hypereosinophilia&atypical lymphocytes •LNE • DRUGS-anticonvulsants,sulpha, dapsone,minocycline, terbinafine • Rx- steroids
  • 43.
    Drug induced pseudolymphoma syndrome •More insidious onset – usually after 7 weeks • Facial edema+ but no fever • Ery. plaques / multiple infiltrative papules / solitary nodule • Rx- drug withdrawal • Anticonvulsants,antipsychotics,antihistamines,CCB,ACEI,beta blocker
  • 44.
    AGEP • Multiple pustuleswith fever mimicking pustular psoriasis • within 24 hrs • Start on face& flexures • penicillin / macrolide