eMedicine Specialties > Pediatrics: General Medicine > Dermatology

Contact Dermatitis: Follow-up

Author: Mark A Crowe, MD, Assistant Clinical Instructor, Department of Medicine, Division of Dermatology, University of Washington School of Medicine
Contributor Information and Disclosures

Updated: Aug 6, 2009

Follow-up

Deterrence/Prevention

  • Prevention of contact dermatitis is better than cure. The most important part of the treatment is to identify and eliminate further exposure to the causative agent.
  • Urushiol is the oily resin in poison ivy, poison sumac, and poison oak, which causes an allergic reaction. Keep in mind this resin can remain active for years on virtually any surface. Thoroughly wash everything that might have brushed against the plants, including clothing, shoes, tools, camping equipment, and pets.
  • Wearing a long-sleeved shirt, pants, gloves, and boots when in an infested area and bathing as soon as possible after exposure are effective methods to limit rhus dermatitis.
  • The only places in the United States where poison ivy is not found are areas above 4000 ft elevation, Alaska, Hawaii, and some desert areas of California and Nevada. Poison ivy usually grows east of the Rocky Mountains and in Canada. Poison oak grows in the western United States, Canada, and Mexico (western poison oak), and in the southeastern states (eastern poison oaks). Poison sumac grows in the eastern states and southern Canada.
  • Learn to recognize poison ivy, poison sumac, and poison oak and have them removed from areas where children are likely to play. Several features of poison ivy, oak, and sumac are useful in identification. Poison ivy and oak may be shrubs or climbing vines. All species of poison ivy and oak have 3 leaflets per leaf, hence the reminder, "Leaves of 3, let them be." The leaf stalk has a groove where it attaches to the branch. Blooms and fruits arise in the angle between the leaf and the branch. Young leaves frequently are reddish in color, and the mature fruit is tan or cream colored. Poison sumac is a shrub or small tree usually 5-10 feet tall and grows in swampy areas or peat bogs. Poison sumac contains 7-13 paired leaflets in a row. The American Academy of Dermatology has handouts with color photographs available for purchase or viewing on their web site.
  • Poison ivy, poison sumac, and poison oak are most dangerous in the spring and summer when plenty of sap is present. The leaves, branches, and trunk may show black marks where they have been injured. The sap turns black after exposure to air.
  • Do not let pets run through wooded areas where poison ivy, poison sumac, and poison oak grow. They may carry urushiol on their fur, causing contact dermatitis in family members who come in contact with the animal. Urushiol can travel in smoke if it burns in a fire; do not burn plants that look like poison ivy, poison sumac, or poison oak.

Complications

  • Secondary bacterial infections are uncommon in the acute stages of contact dermatitis. They may occur several days after damage to the skin and should be treated with systemic antibiotics.
  • Generalized eruptions secondary to autosensitization may occur in association with severe localized allergic contact dermatitis.
  • Pulmonary symptoms may occur following inhalation of irritants or potent allergens.
  • Scar formation may result from deep chemical burns or significant secondary infection.

Prognosis

  • The prognosis of contact dermatitis depends on the cause and the possibility of avoiding repeated or continued exposure to the causal allergen or irritant. Most contact dermatitis resolves without intervention in 4-6 weeks if further exposure is prevented. Obviously, long-term success in treatment is poor if the correct diagnosis and offending agent are not identified.
  • Numerous individual factors are also important in prognosis. Although an alert patient can reduce contact, some ubiquitous allergens, such as rubber or nickel, are quite impossible to totally avoid.
  • Some allergens probably are still unknown, and the significance of others may not be fully realized yet.
  • New sensitivities to topical medications or other substances may develop during the course of dermatitis. Sensitivity to rubber gloves may complicate dermatitis of the hands. Sensitivity to neomycin may complicate the course when applied to an infected dermatitis. During a long course of relapsing dermatitis, sensitivity to various allergens may accumulate, increasing the risk of recurrence.
  • Contact dermatitis of the hands is generally of mixed origin, caused by alternating or simultaneous exposure to allergens and irritants. Half of patients with hand dermatitis have had symptoms of dermatitis for more than 5 years. When followed up after 6-22 months, one quarter of the patients heal completely, half of the patients improve, and one quarter of the patients are unchanged or worse. No difference in prognosis between irritant and allergic dermatitis is observed.
  • Relapses or chronicity is due not only to reexposure to allergens and irritants, but also to other contributory mechanisms.
    • The barrier function of the skin is impaired for months or even years after an episode of dermatitis. Recovery can be prevented by exposure to irritants or allergens in concentrations that may be tolerated by normal skin.
    • Inappropriate treatment with irritants or allergens, such as overzealous use of cleansers and antiseptics, use of various popular or herbal remedies, or both, may prolong the course.
    • Secondary infection is common in chronic contact dermatitis, preventing normal recovery.

Patient Education

  • Patch testing can be extremely important in diagnosing the cause of allergic contact dermatitis; however, patients forget more than 40% of identified allergens. Provide a printed list of sources of allergic contact to the patient. Discuss sources of allergic contact with the same or cross-reacting allergens.
  • Discuss prognosis. Acute allergic contact dermatitis may take several weeks to completely resolve. Recurrences are common unless the contactant is identified and avoided.
  • Provide instructions for reduction of further contact, identification of sources of contactant, barrier protection, good skin care, and hygiene.
  • Allergy does not disappear when the dermatitis clears. Risk of relapses usually persists throughout life.
  • Following significant episodes of dermatitis, the area of involved skin may be especially sensitive to recurrences for several months.
  • Allergic contact dermatitis may be prolonged by subsequent contact with weak irritants. Conversely, patients with irritant dermatitis may develop an undetected secondary allergy to an ingredient of creams or rubber gloves being used to treat the initial dermatitis.
  • Secondary infection is common in subacute or chronic contact dermatitis. If the contact dermatitis is resistant to appropriate therapy or suddenly worsens for no particular reason, secondary bacterial infection should be considered.
  • Urushiol, the allergen in poison ivy, can remain active for months. Exposed clothing, shoes, tools, camping equipment, and pets must be washed thoroughly.
  • If rhus dermatitis is a problem, patients must learn to recognize the plants and have them removed from areas where children are likely to play. The American Academy of Dermatology has handouts with color photographs available for purchase or viewing on their web site.
  • Wearing a long-sleeved shirt, pants, gloves, and boots when in areas infested with poison ivy and bathing as soon as possible after exposure are effective methods for reducing rhus dermatitis.
  • For excellent patient education resources, visit eMedicine’s Skin, Hair, and Nails Center. Also, see eMedicine’s patient education articles Contact Dermatitis and Eczema.

Miscellaneous

Medicolegal Pitfalls

  • Potential sources for exposure to specific allergens and irritants are often extensive. Extensively counsel patients with documented contact dermatitis on possible sources of future exposure. If possible, provide a written list of potential sources. Although listing every potential source of exposure is impossible, provide the patient with the name of the contactant and related chemical compounds. Failure to do so may result in the patient experiencing unnecessary exposure and dermatitis. In cases of extreme sensitivity, exposure may produce severe or fatal reactions.
  • Patients with severe allergies may experience anaphylaxis. Anaphylaxis occurs most commonly in patients who are extremely sensitive to latex and is less common in patients sensitive to exposure to other antigens.
  • Inadvertent exposure to latex in a patient with severe latex allergy may result in adverse outcomes and litigation. Equipment and gloves should be latex-free during clinical examinations and surgical procedures of patients with extreme sensitivity to latex. Failure to obtain a history suggestive of recognized or unrecognized latex allergy may result in adverse outcomes and litigation.
  • Anaphylaxis may occur shortly after application of antigens used in patch testing. This finding is particularly true when testing for latex allergy but may occur with exposure to other antigens.
  • Monitor patients for anaphylactic reactions to antigens used in patch testing. Appropriate resuscitation must be available should anaphylaxis occur during the early stages of patch testing.

Special Concerns

  • Occupational contact dermatitis is a major problem.9 Patients may need assistance with positively identifying irritants or allergens in the work place. Once identified, the patient's environment must be appropriately adjusted. Patients may need assistance with documentation for worker's compensation claims.
  • Although some studies suggest an increased incidence of allergic contact dermatitis exists in atopic patients, most recent studies suggest incidence of allergic contact dermatitis in atopic patients is similar to that of patients experiencing other conditions, such as seborrheic dermatitis. Some evidence suggests that atopic patients may be less easily sensitized than other groups. Patients with severe atopic dermatitis, in fact, may have a diminished capacity for dinitrochlorobenzene (DNCB) sensitization. Atopic patients are also more susceptible to irritant patch test reactions, especially when testing with metals. This may lead to false-positive results from routine patch testing. In a study of 101 sets of twins, no correlation was found between positive patch test results and atopy.
  • Investigators have found that most people could be immunized against poison ivy through prescription pills; however, this procedure can take months to achieve a reasonable degree of hyposensitization and must be continued over a long period. Immunization can cause uncomfortable side effects and should only be considered for individuals, such as firefighters, who must live or work in areas where they come into constant contact with poison ivy.
 


More on Contact Dermatitis

Overview: Contact Dermatitis
Differential Diagnoses & Workup: Contact Dermatitis
Treatment & Medication: Contact Dermatitis
Follow-up: Contact Dermatitis
Multimedia: Contact Dermatitis
References

References

  1. Lee PW, Elsaie ML, Jacob SE. Allergic contact dermatitis in children: common allergens and treatment: a review. Curr Opin Pediatr. Aug 2009;21(4):491-8. [Medline].

  2. Militello G, Jacob SE, Crawford GH. Allergic contact dermatitis in children. Curr Opin Pediatr. Aug 2006;18(4):385-90. [Medline].

  3. Fisher AA, Rietschel RL, Fowler JF. Fisher's Contact Dermatitis. 4th ed. Philadelphia, PA: Lippincott, Williams & Wilkins; 1995.

  4. Warshaw E, Lee G, Storrs FJ. Hand dermatitis: a review of clinical features, therapeutic options, and long-term outcomes. Am J Contact Dermat. Sep 2003;14(3):119-37. [Medline].

  5. Brasch J, Geier J. Patch test results in schoolchildren. Results from the Information Network of Departments of Dermatology (IVDK) and the German Contact Dermatitis Research Group (DKG). Contact Dermatitis. Dec 1997;37(6):286-93. [Medline].

  6. de Lagran ZM, de Frutos FJ, de Arribas MG, Vanaclocha-Sebastian F. Contact urticaria to raw potato. Dermatol Online J. May 15 2009;15(5):14. [Medline].

  7. Clemmensen O, Hjorth N. Perioral contact urticaria from sorbic acid and benzoic acid in a salad dressing. Contact Dermatitis. Jan 1982;8(1):1-6. [Medline].

  8. [Guideline] American Academy of Allergy, Asthma and Immunology; American College of Allergy, Asthma and Immunology. Contact dermatitis: a practice parameter. Ann Allergy Asthma Immunol. Sep 2006;97(3 Suppl 2):S1-38. [Medline].

  9. Raikhlin-Eisenkraft B. Contact dermatitis from occupation-induced injury. Isr Med Assoc J. May 2009;11(5):322. [Medline].

  10. Ayala F, Balato N, Lembo G, et al. A multicentre study of contact sensitization in children. Gruppo Italiano Ricerca Dermatiti da Contatto e Ambientali (GIRDCA). Contact Dermatitis. May 1992;26(5):307-10. [Medline].

  11. Azurdia RM, King CM. Allergic contact dermatitis due to phenol-formaldehyde resin and benzoyl peroxide in swimming goggles. Contact Dermatitis. Apr 1998;38(4):234-5. [Medline].

  12. Barros MA, Baptista A, Correia TM, Azevedo F. Patch testing in children: a study of 562 schoolchildren. Contact Dermatitis. Sep 1991;25(3):156-9. [Medline].

  13. Basketter DA, Jefferies D, Safford BJ, et al. The impact of exposure variables on the induction of skin sensitization. Contact Dermatitis. Sep 2006;55(3):178-85. [Medline].

  14. Beattie PE, Green C, Lowe G, Lewis-Jones MS. Which children should we patch test?. Clin Exp Dermatol. Jan 2007;32(1):6-11. [Medline].

  15. Belsito D, Wilson DC, Warshaw E, et al. A prospective randomized clinical trial of 0.1% tacrolimus ointment in a model of chronic allergic contact dermatitis. J Am Acad Dermatol. Jul 2006;55(1):40-6. [Medline].

  16. Belsito DV, Fowler JF Jr, Sasseville D, et al. Delayed-type hypersensitivity to fragrance materials in a select North American population. Dermatitis. Mar 2006;17(1):23-8. [Medline].

  17. Berne B, Bostrom A, Grahnen AF, Tammela M. Adverse effects of cosmetics and toiletries reported to the Swedish Medical Products Agency 1989-1994. Contact Dermatitis. May 1996;34(5):359-62. [Medline].

  18. Brancaccio RR, Brown LH, Chang YT, et al. Identification and quantification of para-phenylenediamine in a temporary black henna tattoo. Am J Contact Dermat. Mar 2002;13(1):15-8. [Medline].

  19. Brown T. Strategies for prevention: occupational contact dermatitis. Occup Med (Lond). Oct 2004;54(7):450-7. [Medline].

  20. Bruynzeel DP, Ferguson J, Andersen K, et al. Photopatch testing: a consensus methodology for Europe. J Eur Acad Dermatol Venereol. Nov 2004;18(6):679-82. [Medline].

  21. Bryden AM, Moseley H, Ibbotson SH, et al. Photopatch testing of 1155 patients: results of the U.K. multicentre photopatch study group. Br J Dermatol. Oct 2006;155(4):737-47. [Medline].

  22. Burden AD, Beck MH. Contact hypersensitivity to topical corticosteroids. Br J Dermatol. Nov 1992;127(5):497-500. [Medline].

  23. Clayton TH, Wilkinson SM, Rawcliffe C, Pollock B, Clark SM. Allergic contact dermatitis in children: should pattern of dermatitis determine referral? A retrospective study of 500 children tested between 1995 and 2004 in one U.K. centre. Br J Dermatol. Jan 2006;154(1):114-7. [Medline].

  24. Cockayne SE, Shah M, Messenger AG, Gawkrodger DJ. Foot dermatitis in children: causative allergens and follow-up. Contact Dermatitis. Apr 1998;38(4):203-6. [Medline].

  25. Codreanu F, Morisset M, Cordebar V, Kanny G, Moneret-Vautrin DA. Risk of allergy to food proteins in topical medicinal agents and cosmetics. Allerg Immunol (Paris). Apr 2006;38(4):126-30. [Medline].

  26. Cohen DE, Heidary N. Treatment of irritant and allergic contact dermatitis. Dermatol Ther. 2004;17(4):334-40. [Medline].

  27. Davis MD, el-Azhary RA, Farmer SA. Results of patch testing to a corticosteroid series: a retrospective review of 1188 patients during 6 years at Mayo Clinic. J Am Acad Dermatol. Jun 2007;56(6):921-7. [Medline].

  28. De Groot AC. Patch Testing: Test Concentrations and Vehicles for 3700 Chemicals. 2nd ed. New York, NY: Elsevier Science Ltd; 1994.

  29. de Waard-van der Spek FB, Oranje AP. Purpura caused by Emla is of toxic origin. Contact Dermatitis. Jan 1997;36(1):11-3. [Medline].

  30. Dubakiene R, Kupriene M. Scientific problems of photosensitivity. Medicina (Kaunas). 2006;42(8):619-24. [Medline].

  31. Farage MA. Are we reaching the limits or our ability to detect skin effects with our current testing and measuring methods for consumer products?. Contact Dermatitis. Jun 2005;52(6):297-303. [Medline].

  32. Fisher AA. Allergic contact dermatitis in early infancy. Cutis. Nov 1994;54(5):300-2. [Medline].

  33. Fisher AA. Perfume dermatitis in children sensitized to balsam of Peru in topical agents. Cutis. Jan 1990;45(1):21-3. [Medline].

  34. Fotiades J, Soter NA, Lim HW. Results of evaluation of 203 patients for photosensitivity in a 7.3-year period. J Am Acad Dermatol. Oct 1995;33(4):597-602. [Medline].

  35. Goncalo S, Goncalo M, Azenha A, et al. Allergic contact dermatitis in children. A multicenter study of the Portuguese Contact Dermatitis Group (GPEDC). Contact Dermatitis. Feb 1992;26(2):112-5. [Medline].

  36. Goon AT, Goh CL. Patch testing of Singapore children and adolescents: our experience over 18 years. Pediatr Dermatol. Mar-Apr 2006;23(2):117-20. [Medline].

  37. Guerra L, Rogkakou A, Massacane P, et al. Role of contact sensitization in chronic urticaria. J Am Acad Dermatol. Jan 2007;56(1):88-90. [Medline].

  38. Guin JD. The black spot test for recognizing poison ivy and related species. J Am Acad Dermatol. Apr 1980;2(4):332-3. [Medline].

  39. Guin JD, Gillis WT, Beaman JH. Recognizing the Toxicodendrons (poison ivy, poison oak, and poison sumac). J Am Acad Dermatol. Jan 1981;4(1):99-114. [Medline].

  40. Hanks JW, Venters WJ. Nickel allergy from a bed-wetting alarm confused with herpes genitalis and child abuse. Pediatrics. Sep 1992;90(3):458-60. [Medline].

  41. Harvell J, Bason M, Maibach H. Contact urticaria and its mechanisms. Food Chem Toxicol. Feb 1994;32(2):103-12. [Medline].

  42. Hemmer W, Focke M, Gotz M, Jarisch R. Pigmented contact dermatitis of the lips from a lipstick. Contact Dermatitis. Nov 1997;37(5):244. [Medline].

  43. Hogan PA, Weston WL. Allergic contact dermatitis in children. Pediatr Rev. Jun 1993;14(6):240-3. [Medline].

  44. Humphrey S, Bergman JN, Au S. Practical management strategies for diaper dermatitis. Skin Therapy Lett. Sep 2006;11(7):1-6. [Medline].

  45. Jacob SE, Amado A, Cohen DE. Dermatologic surgical implications of allergic contact dermatitis. Dermatol Surg. Sep 2005;31(9 Pt 1):1116-23. [Medline].

  46. Jasim ZF, Darling JR, Handley JM. Severe allergic contact dermatitis to paraphenylene diamine in hair dye following sensitization to black henna tattoos. Contact Dermatitis. Feb 2005;52(2):116-7. [Medline].

  47. Kandil HH, al-Ghanem MM, Sarwat MA, al-Thallab FS. Henna (Lawsonia inermis Linn.) inducing haemolysis among G6PD-deficient newborns. A new clinical observation. Ann Trop Paediatr. Dec 1996;16(4):287-91. [Medline].

  48. Katsarou A, Koufou V, Armenaka M, et al. Patch tests in children: a review of 14 years experience. Contact Dermatitis. Jan 1996;34(1):70-1. [Medline].

  49. Kim E, Maibach H. Changing paradigms in dermatology: science and art of diagnostic patch and contact urticaria testing. Clin Dermatol. Sep-Oct 2003;21(5):346-52. [Medline].

  50. Kok AN, Ertekin V, Bilge Y, Isik AF. An unusual cause of suicide: henna (Lawsonia inermis Linn.). J Emerg Med. Oct 2005;29(3):343-4. [Medline].

  51. Kriechbaumer N, Hemmer W, Focke M, et al. Sensitization to ethyl chloride in a handball player. Contact Dermatitis. Apr 1998;38(4):227-8. [Medline].

  52. Kwangsukstith C, Maibach HI. Effect of age and sex on the induction and elicitation of allergic contact dermatitis. Contact Dermatitis. Nov 1995;33(5):289-98. [Medline].

  53. Lever R, Forsyth A. Allergic contact dermatitis in atopic dermatitis. Acta Derm Venereol Suppl (Stockh). 1992;176:95-8. [Medline].

  54. Lutsky BN, Schuller JL, Cerio R, et al. Comparative study of the efficacy and safety of loratadine syrup and terfenadine suspension in the treatment of chronic allergic skin diseases in a pediatric population. Arzneimittelforschung. Nov 1993;43(11):1196-9. [Medline].

  55. Manzini BM, Ferdani G, Simonetti V, et al. Contact sensitization in children. Pediatr Dermatol. Jan-Feb 1998;15(1):12-7. [Medline].

  56. Matulich J, Sullivan J. A temporary henna tattoo causing hair and clothing dye allergy. Contact Dermatitis. Jul 2005;53(1):33-6. [Medline].

  57. McAlvany JP, Sherertz EF. Contact dermatitis in infants, children, and adolescents. Adv Dermatol. 1994;9:205-23; discussion 224. [Medline].

  58. Murphy GM. Investigation of photosensitive disorders. Photodermatol Photoimmunol Photomed. Dec 2004;20(6):305-11. [Medline].

  59. Neri I, Savoia F, Guareschi E, Medri M, Patrizi A. Purpura after application of EMLA cream in two children. Pediatr Dermatol. Nov-Dec 2005;22(6):566-8. [Medline].

  60. Oh-i T. Contact dermatitis due to topical steroids with conceivable cross reactions between topical steroid preparations. J Dermatol. Mar 1996;23(3):200-8. [Medline].

  61. Oranje AP, Aarsen RS, Mulder PG, et al. Food immediate-contact hypersensitivity (FICH) and elimination diet in young children with atopic dermatitis. Preliminary results in 107 children. Acta Derm Venereol Suppl (Stockh). 1992;176:- van Toorenenbergen AW. [Medline].

  62. Oranje AP, Aarsen RS, Mulder PG, Liefaard G. Immediate contact reactions to cow's milk and egg in atopic children. Acta Derm Venereol. 1991;71(3):263-6. [Medline].

  63. Oranje AP, Bruynzeel DP, Stenveld HJ, Dieges PH. Immediate- and delayed-type contact hypersensitivity in children older than 5 years with atopic dermatitis: a pilot study comparing different tests. Pediatr Dermatol. Sep 1994;11(3):209-15. [Medline].

  64. Orton DI, Wilkinson JD. Cosmetic allergy: incidence, diagnosis, and management. Am J Clin Dermatol. 2004;5(5):327-37. [Medline].

  65. Pacor ML, Di Lorenzo G, Martinelli N, Mansueto P, Friso S, Pellitteri ME. Tacrolimus ointment in nickel sulphate-induced steroid-resistant allergic contact dermatitis. Allergy Asthma Proc. Nov-Dec 2006;27(6):527-31. [Medline].

  66. Pambor M, Kruger G, Winkler S. Results of patch testing in children. Contact Dermatitis. Nov 1992;27(5):326-8. [Medline].

  67. Pambor M, Winkler S, Bloch Y. Allergic contact dermatitis in children. Contact Dermatitis. Jan 1991;24(1):72-4. [Medline].

  68. Patil S, Maibach HI. Effect of age and sex on the elicitation of irritant contact dermatitis. Contact Dermatitis. May 1994;30(5):257-64. [Medline].

  69. Pegas JR, Criado PR, Criado RF, Vasconcellos C, Pires MC. Allergic contact dermatitis to temporary tattoo by p-phenylenediamine. J Investig Allergol Clin Immunol. 2002;12(1):62-4. [Medline].

  70. Potasman I, Heinrich I, Bassan HM. Aquagenic pruritus: prevalence and clinical characteristics. Isr J Med Sci. Sep 1990;26(9):499-503. [Medline].

  71. Rasanen L, Lehto M, Mustikka-Maki UP. Sensitization to nickel from stainless steel ear-piercing kits. Contact Dermatitis. May 1993;28(5):292-4. [Medline].

  72. Redlick F, DeKoven J. Allergic contact dermatitis to paraphenylendiamine in hair dye after sensitization from black henna tattoos: a report of 6 cases. CMAJ. Feb 13 2007;176(4):445-6. [Medline].

  73. Rietschel RL. Clues to an accurate diagnosis of contact dermatitis. Dermatol Ther. 2004;17(3):224-30. [Medline].

  74. Roul S, Ducombs G, Leaute-Labreze C, et al. Footwear contact dermatitis in children. Contact Dermatitis. Dec 1996;35(6):334-6. [Medline].

  75. Rudzki E, Rebandel P. Contact dermatitis in children. Contact Dermatitis. Jan 1996;34(1):66-7. [Medline].

  76. Rycroft RJG, Menne T, Frosch PJ. Textbook of Contact Dermatitis. 2nd ed. New York, NY: Springer Verlag; 1994.

  77. Satyawan I, Oranje AP, van Joost T. Perioral dermatitis in a child due to rosin in chewing gum. Contact Dermatitis. Mar 1990;22(3):182-3. [Medline].

  78. Schauder S, Ippen H. Contact and photocontact sensitivity to sunscreens. Review of a 15-year experience and of the literature. Contact Dermatitis. Nov 1997;37(5):221-32. [Medline].

  79. Seidenari S, Manzini BM, Danese P. Contact sensitization to textile dyes: description of 100 subjects. Contact Dermatitis. Apr 1991;24(4):253-8. [Medline].

  80. Sevila A, Romaguera C, Vilaplana J, Botella R. Contact dermatitis in children. Contact Dermatitis. May 1994;30(5):292-4. [Medline].

  81. Shah M, Lewis FM, Gawkrodger DJ. Patch testing in children and adolescents: five years' experience and follow-up. J Am Acad Dermatol. Dec 1997;37(6):964-8. [Medline].

  82. Shivaram V, Christoph RA, Hayden GF. Skin disorders encountered in a pediatric emergency department. Pediatr Emerg Care. Aug 1993;9(4):202-4. [Medline].

  83. Sosted H, Johansen JD, Andersen KE, Menne T. Severe allergic hair dye reactions in 8 children. Contact Dermatitis. Feb 2006;54(2):87-91. [Medline].

  84. Stables GI, Forsyth A, Lever RS. Patch testing in children. Contact Dermatitis. May 1996;34(5):341-4. [Medline].

  85. Torgerson RR, Davis MD, Bruce AJ, Farmer SA, Rogers RS 3rd. Contact allergy in oral disease. J Am Acad Dermatol. Aug 2007;57(2):315-21. [Medline].

  86. Trevisan G, Kokelj F. Allergic contact dermatitis due to shoes in children: a 5-year follow-up. Contact Dermatitis. Jan 1992;26(1):45. [Medline].

  87. Wantke F, Focke M, Hemmer W, et al. Generalized urticaria induced by a diethyltoluamide-containing insect repellent in a child. Contact Dermatitis. Sep 1996;35(3):186-7. [Medline].

  88. Wantke F, Hemmer W, Jarisch R, Gotz M. Patch test reactions in children, adults and the elderly. A comparative study in patients with suspected allergic contact dermatitis. Contact Dermatitis. May 1996;34(5):316-9. [Medline].

  89. Watemberg N, Urkin Y, Witztum A. Phytophotodermatitis due to figs. Cutis. Aug 1991;48(2):151-2. [Medline].

  90. Weston WL. Contact dermatitis in children. Curr Opin Pediatr. Aug 1997;9(4):372-6. [Medline].

  91. Wilkowska A, Grubska-Suchanek E, Karwacka I, Szarmach H. Contact allergy in children. Cutis. Aug 1996;58(2):176-80. [Medline].

  92. Wolf R, Wolf D, Matz H, Orion E. Cutaneous reactions to temporary tattoos. Dermatol Online J. Feb 2003;9(1):3. [Medline].

Further Reading

Keywords

contact dermatitis, allergic contact dermatitis, ACD, dermatitis venenata, contact eczema, rhus dermatitis, poison ivy, poison oak, poison sumac, irritant contact dermatitis, ICD, primary irritant dermatitis, photo contact dermatitis, photoallergic contact dermatitis, phototoxic contact dermatitis, berloque dermatitis, contact urticaria, hives, whelps, eczematous dermatitis, acute caustic burn, cold urticaria, cholinergic urticaria, dermatographism, pressure urticaria, aquagenic pruritus, aquagenic urticaria, solar urticaria, heat urticaria, papular urticaria, exercise-induced urticaria, latex allergy, sunburn, nickel allergy, hyperpigmentation, folliculitis, melanoderma, Umbelliferae family

Contributor Information and Disclosures

Author

Mark A Crowe, MD, Assistant Clinical Instructor, Department of Medicine, Division of Dermatology, University of Washington School of Medicine
Mark A Crowe, MD is a member of the following medical societies: American Academy of Dermatology and North American Clinical Dermatologic Society
Disclosure: Nothing to disclose.

Medical Editor

Kevin P Connelly, DO, Clinical Assistant Professor, Department of Pediatrics, Division of General Pediatrics and Emergency Care, Virginia Commonwealth University; Medical Director, Paws for Health Pet Visitation Program of the Richmond SPCA; Pediatric Emergency Physician, Emergency Consultants Inc, Chippenham Medical Center
Kevin P Connelly, DO is a member of the following medical societies: American Academy of Pediatrics, American College of Osteopathic Pediatricians, and American Osteopathic Association
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Robert A Schwartz, MD, MPH, Professor and Head, Dermatology, Professor of Pathology, Pediatrics, Medicine, and Preventive Medicine and Community Health, UMDNJ-New Jersey Medical School
Robert A Schwartz, MD, MPH is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, American College of Physicians, and Sigma Xi
Disclosure: Nothing to disclose.

CME Editor

Merrily P M Poth, MD, Professor, Department of Pediatrics and Neuroscience, Uniformed Services University of the Health Sciences
Merrily P M Poth, MD is a member of the following medical societies: American Academy of Pediatrics, Endocrine Society, and Lawson-Wilkins Pediatric Endocrine Society
Disclosure: Nothing to disclose.

Chief Editor

Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center
Dirk M Elston, MD is a member of the following medical societies: American Academy of Dermatology
Disclosure: Nothing to disclose.

 
 
HONcode

We subscribe to the
HONcode principles of the
Health On the Net Foundation

All material on this website is protected by copyright, Copyright© 1994- by Medscape.
This website also contains material copyrighted by 3rd parties.

DISCLAIMER: The content of this Website is not influenced by sponsors. The site is designed primarily for use by qualified physicians and other medical professionals. The information contained herein should NOT be used as a substitute for the advice of an appropriately qualified and licensed physician or other health care provider. The information provided here is for educational and informational purposes only. In no way should it be considered as offering medical advice. Please check with a physician if you suspect you are ill.