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Jesus, made changes sa last slide (table) and the circles (site of predilection). Do we need to distinguish kung EM Minor or Major ung patient?. ERYTHEMA MULTIFORME. Erythema Multiforme. EM minor & EM with mucosal involvement Self-limited, recurrent disease
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Jesus, made changes sa last slide (table) and the circles (site of predilection) Do we need to distinguish kung EM Minor or Major ung patient?
Erythema Multiforme EM minor & EM with mucosal involvement • Self-limited, recurrent disease • No or only a mild prodrome (1 to 4 weeks) • Sharply marginatederythematousmacules become raised, edematous papules (24 to 48 hours) • Koebner’s phenomenon or photoaccentuation • Mucosal involvement in 25% -- usually limited to the oral mucosa • More severe classic case? Two or more mucous membranes involved in 45%
EM Minor Characteristic & Evolution of the Lesion • Periphery: ring of erythema • Central: flatters, more pruritic and dusky • “target” or “iris” lesion with three zones • Central dusky purpura • Elevated, edematous, pale ring • Surrounding macular erythema
EM Minor Sites of Predilection (Symmetrical and acral) • (Best observed on) Palms and soles • Dorsal feet • Extensor limbs • Elbows • Knees Age of Predilection • young adults
Erythema Multiforme Steven-Johnson syndrome / EM major • Clinically different from minor • Frequently, febrile prodrome
EM Major Characteristic & Evolution of the Lesion • Flat, erythematous or purpuric macules incomplete “atypical targets” (may blister centrally • Larger and more commonly confluent lesions compared to EM minor
EM Major Sites of Predilection • Begins diffusely on the trunk and mucous membranes • Spreads centripetally Age of Predilection • Eruption occurs at all ages
Etiologic Factors • EM minor = herpes simplex infection • Typically orolabial • 1 to 3 weeks (10 day average) after herpes lesion • May or not follow herpes outbreaks • EM major(SJS) = medications • Most centrally accentuated eruptions with atypical targets • Sulfonamides, antibiotics, NSAIDs, allopurinol, anticonvulsants • Due to abnormal metabolism of medications
Etiologic Factors • Also, EM major= Mycoplasmapneumoniae • Prominent mucosal involvement and bullous skin lesions – NOT classic iris lesions • Resemble SJS cases • And, EM major = radiation therapy • With phenytoin and tapering corticosteroids – induces EM starting at radiation port
Pathogenesis • Activated T lymphocytes • Epidermis: cytotoxic or suppressor cells • Dermis: helper T cells • EM minor – specific HLA types (HLA-DQ3) • SJS – abnormalities in drug metabolism Hence, there is a genetic component for both diseases
Disease Diagnosis • Physical examination • Characteristic Target Lesions • Distribution- symmetrical and acral • Evolution: Center becomes darker and purpuric Lesions flatten at the center Ring of Erythema