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CONTACT DERMATITIS

CONTACT DERMATITIS. (49) Marienelle R. Maulion Section C Group 5. Contact Dermatitis. The generic term applied to acute and chronic inflammatory reactions to substances that come in contact with the skin Acute dermatitis : pruritus, erythema, and vesiculation

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CONTACT DERMATITIS

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  1. CONTACT DERMATITIS (49) Marienelle R. Maulion Section C Group 5

  2. Contact Dermatitis • The generic term applied to acute and chronic inflammatory reactions to substances that come in contact with the skin • Acute dermatitis: pruritus, erythema, and vesiculation • Chronic dermatitis: pruritus, xerosis, lichenification, hyperkeratosis, and/or fissuring

  3. Regional Sites of Predilection

  4. Tests for Sensitivity PATCH TEST • To detect hypersensitivity to a substance that is in contact with skin so that the allergen may be determined and corrective measures taken

  5. Tests for Sensitivity Provocative Use Test • Confirms a positive closed patch test reaction to ingredients of a substance; to test products that are made to stay on the skin once applied Photopatch Test • To evaluate for contact photoallergy to such substances as sulfonamides, phenothiazines, PABA, oxybenzone, musk ambrette

  6. Types of Contact Dermatitis Irritant Contact Dermatitis • An inflammatory reaction in the skin resulting from exposure to a substance that causes an eruption in most people who come in contact with it Allergic Contact Dermatitis • An acquired delayed sensitivity to various substances that produce inflammatory reactions in only those who have been previously sensitized to the allergen

  7. Irritant Contact Dermatitis Etiologic Agents • Water, soaps, detergents, bleaches, lye, drain pipe cleaners, toilet bowl and oven cleansers • Acids and Alkalis • Solvents and Hydrocarbons • Fiberglass, dust, capsaicin, teargas, metal salts Predisposing Factors • History of atopic dermatitis • Occupational exposure/ Repeated exposure • Low temperature/ Low humidity • Condition of the skin

  8. Irritant Contact Dermatitis Pathogenesis • The irritants cause cell damage if applied for sufficient time and in adequate concentration. Inflammatory response occurs because of the inability of the skin to defend and repair its integrity and function from penetrating chemicals.

  9. Irritant Contact Dermatitis Acute Irritant Contact Dermatitis • Burning, stinging, painful sensations can occur immediately within seconds after exposure or may be delayed up to 24 hour LESION Erythema with a dull, nonglistening surface  vesiculation (blister formation)  erosion  crusting  shedding of crusts and scaling or erythema necrosis  shedding of necrotic tissue  ulceration  healing

  10. Irritant Contact Dermatitis Acute Irritant Contact Dermatitis

  11. Irritant Contact Dermatitis Acute Irritant Contact Dermatitis

  12. Irritant Contact Dermatitis Chronic Irritant Contact Dermatitis • Prolonged and repeated exposures of the skin to irritants results to a chronic disturbance of the barrier function, subsequently, elicit a chronic inflammatory response. • Stinging and itching, pain as fissures develop LESION Dryness  chapping erythema hyperkeratosis and scaling  fissures and crusting • Lichenification, vesicles, pustules, and erosions

  13. Irritant Contact Dermatitis Chronic Irritant Contact Dermatitis

  14. Allergic Contact Dermatitis Etiologic Agents/Allergens • Poison Ivy, raw cashew nuts, mango, chrysanthemum, pollens, castor bean, latex of fig and rubber trees • Fabric finishers, dyes, rubber additives, anti-wrinking and crease-holding chemicals, brassieres, tight clothes • Rubber accelerators, leathers, adhesives, foam rubber padding, felt, cork liners, formaldehyde in shoes • Nickel-containing (earrings, watch), Chromate (paint, gloves), Mercury (waving solution, amalgams), Cobalt (paints, glass), Arsenic (fabric dyes, disinfectants), Gold (dental gold, gold jewelry contaminated with radon) • Fragrance, cosmetic preservatives, permanent hair dye, acid permanent wave preparation, sunscreens, mechanical hair removers, nail lacquers, deodorants

  15. Allergic Contact Dermatitis Pathogenesis

  16. Allergic Contact Dermatitis Acute Allergic Contact Dermatitis • Well-demarcated erythema and edema on which are superimposed closely spaced, nonumbilicated vesicles, and/or papules LESION: ErythemaPapules vesicles erosions crusts scaling.

  17. Allergic Contact Dermatitis Acute Allergic Contact Dermatitis

  18. Allergic Contact Dermatitis Acute Allergic Contact Dermatitis

  19. Allergic Contact Dermatitis Chronic Allergic Contact Dermatitis • Plaques of lichenification (thickening of the epidermis with deepening of the skin lines in parallel or rhomboidal pattern), scaling with satellite, small, firm, rounded or flat-topped papules, excoriations, erythema, and pigmentation LESION Papules scalinglichenification excoriations

  20. Allergic Contact Dermatitis Chronic Allergic Contact Dermatitis

  21. Allergic Contact Dermatitis Chronic Allergic Contact Dermatitis

  22. Management for Contact Dermatitis Prevention • Avoid exposure to potential allergen • Avoid repeated and prolonged exposure to irritants • Wear protective clothing • Check skin reactions to cosmetics before applying

  23. Management for Contact Dermatitis Treatment for Irritant Contact Dermatitis • Identify and remove the etiologic agent • Wet dressings with gauze soaked in Burow's solution, changed every 2 to 3 hours • Larger vesicles may be drained, but tops should not be removed • Topical class I glucocorticoid preparations • Severe cases: systemic glucocorticoids • Prednisone, 2-week course, 60 mg initially, tapering by steps of 10 mg

  24. Management for Contact Dermatitis Treatment for Allergic Contact Dermatitis • Identify and remove the etiologic agent. • Topical glucocorticoid ointments/gels (classes I to III) for early nonbullous lesions • Larger vesicles may be drained, but tops should not be removed • Wet dressings with cloths soaked in Burow's solution changed every 2 to 3 hours • Systemic glucocorticoids: Severe & Exudative lesions • Prednisone, initial 70 mg (adults), tapering by 5 to 10 mg/d over a 1- to 2-week period.

  25. Thank you.

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