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DERMATOLOGY
1. Erythema Multiforme
2. Stevens-Johnson Syndrome and
Toxic Epidermal Necrolysis
3. Acute Urticaria & Angioedema
4. Exfoliative Erythroderma Syndrome
5. Staphylococcal Scalded Skin Syndrome
ERYTHEMA MULTIFORME
- infection : mycoplasma
- idiopathic : >50%
ERYTHEMA MULTIFORME
Physical exam:
EM Minor :
litle, mucous membrane (-), systemic symp (-) Skin
lesion : developed ≥ 10 d
dull red macule (48h)
↓
papule
↓
vesicles & bullae in center of the papule
(iris, target like lesion)
EM Major
ERYTHEMA MULTIFORME
DD : psoriasis, secondary syphilis,
urticaria.
Tx : glucocorticoid → prednisone 50-
80mg/d →quickly tapered
STEVENS-JOHNSON SYNDROME &
TOXIC EPIDERMAL NECROLYSIS
Def :
mucocutaneous drug-induced or idiophatic
reaction patterns characterized by skin
tenderness and erythema of skin and mucousa,
followed by extensive cutaneous and mucosal
epidermal necrotisand sloughing
→ potentially life-threatening due to
multisystem involvement
STEVENS-JOHNSON SYNDROME
&
TOXIC EPIDERMAL NECROLYSIS
Physical exam :
- prodromal rash : morbiliform, EM-like, diffuse erythema
- early : necrotic epidermis → macule with crinkled
surface → enlarge and coalesce → raised flaccid
blisters (Niklosky sign +)
STEVENS-JOHNSON
SYNDROME
STEVENS-JOHNSON SYNDROME
&
TOXIC EPIDERMAL NECROLYSIS
DD :
- early : EM major, exanthematous drug
eruption, scarlet fever, phototoxic
eruptions.
- fully evolved : EM major thermal burns,
SSSS, generalized bullous fixed drug
eruption, exfoliative dermatitis.
Management :
- withdrawal of suspected drugs
- best cared in intensive care unit
- manage replacement of IV fluids &
electrolytes ~III degree thermal burn
- syst glucocorticoid →high doses & early
- high doses iv immunoglobulin → TEN
- suction frequently → oropharyngeal
involvement
- treat complicating inf
- treat eye lesions →erythromycin oint
ACUTE URTICARIA AND ANGIOEDEMA
Def :
vascular reaction of the skin (trancient
edematous papules and plaques, usualy
pruritic) cause by local intercelular edema that
limited on the skin and mucousa.
ACUTE URTICARIA AND ANGIOEDEMA
Patogenesis :
mast cell & basophil
immunology non immunology (cholinergik efect, physic
(hypersensitivity type I,type III) agent, chemical histamin liberator)
histamin
↓
↑capilary permeability&vasodilatation
↓
liquid transudation
ACUTE URTICARIA AND ANGIOEDEMA
Clinical type :
- acute : acute onset & recurring over
<30 d → large wheals, associated
with angioedema →IgE dependent
Physical exam:
sharply defined wheals, small-large,
erythematous/white with an
erythematous rim, round, oval,
acriform, anular, serpiginous →
confluence
Management :
- Prevention : elimination of etiol
- Histamin H1 blocker
- Prednisone