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Stevens-Johnson Syndrome : A Case Report

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초록

Stevens-Johnson syndrome (SJS), an extremely severe acute hypersensitivity reaction, causes extensive necrosis on the skin and the mucous membrane. SJS is a disease of unknown cause that can occur in all age groups. It is thought to be caused by drug allergy or induced by bacterial infection. Epidermal surface invasion of less than 10 percent is called SJS, and invasion of more than 30 percent is called toxic epidermal necrolysis. Although it is rare with an incidence of 1 - 2 cases per million people per year, it has effects on tooth development and therefore on children who are in a growth phase. The purpose of this case report is to examine the effect of SJS on tooth development in children. In general, eruption of the upper and lower 1st molars and lower central incisors starts at 6 - 7 years of age. Root development also occurs at this time. In the case reported here, SJS occurred in a 6-year-old patient. Although the patient's SJS was completely cured , he still suffers from aftereffects. Developmental abnormalities in the patient’s teeth were observed only in teeth for which root development had been completed at the time. The purpose of this case report is to illustrate how to diagnose such systemic diseases by intra-oral features and to recognize and resolve tooth development problems associated with the disease.

Abstract

Stevens-Johnson syndrome (SJS), an extremely severe acute hypersensitivity reaction, causes extensive necrosis on the skin and the mucous membrane. SJS is a disease of unknown cause that can occur in all age groups. It is thought to be caused by drug allergy or induced by bacterial infection. Epidermal surface invasion of less than 10 percent is called SJS, and invasion of more than 30 percent is called toxic epidermal necrolysis. Although it is rare with an incidence of 1 - 2 cases per million people per year, it has effects on tooth development and therefore on children who are in a growth phase. The purpose of this case report is to examine the effect of SJS on tooth development in children. In general, eruption of the upper and lower 1st molars and lower central incisors starts at 6 - 7 years of age. Root development also occurs at this time. In the case reported here, SJS occurred in a 6-year-old patient. Although the patient's SJS was completely cured , he still suffers from aftereffects. Developmental abnormalities in the patient’s teeth were observed only in teeth for which root development had been completed at the time. The purpose of this case report is to illustrate how to diagnose such systemic diseases by intra-oral features and to recognize and resolve tooth development problems associated with the disease.

참고문헌 (22)

  1. Borchers AT, "Stevens-Johnson syndrome and toxic epidermal necrolysis", Autoimmun Rev, 7, pp.598~605 (2008)
  2. Łoboda J, "Stevens-Johnson syndrome and toxic epidermal necrolysis-based on literature", Przegl Lek, 72, pp.35~37 (2015)
  3. Tristani-Firouzi P, "Treatment of toxic epidermal necrolysis with intravenous immunoglobulin in children", J Am Acad Dermatol, 47, pp.548~552 (2002)
  4. Prins C, "Treatment of toxic epidermal necrolysis with high-dose intravenous immunoglobulins:multicenter retrospective analysis of 48 consecutive cases", Arch Dermatol, 139, pp.26~32 (2003)
  5. Auquier-Dunant A, "Correlations between clinical patterns and causes of erythema multiforme majus, Stevens-Johnson syndrome, and toxic epidermal necrolysis: results of an international prospective study", Arch Dermatol, 138, pp.1019~1024 (2002)
  6. Harr T, "Stevens-Johnson syndrome and toxic epidermal necrolysis", Chem Immunol Allergy, 97, pp.149~166 (2012)
  7. KDA Textbook editing board, "Dermatology", pp.221~227 (2008), Ryomoongak
  8. Bajaj N, "Cessation in root development:ramifications of 'Stevens-Johnson' syndrome", J Indian Soc Pedod Prev Dent, 30, pp.267~270 (2012)
  9. De Man K, "Abnormal root development, probably due to erythema multiforme (Stevens-Johnson syndrome)", Int J Oral Surg, 8, pp.381~385 (1997)
  10. Brook U, "Stevens-Johnson syndrome and abnormal root development: a case report", Int J Paediatr Dent, 4, pp.101~103 (1994)
  11. LIBRACH IM, "Erythema multiforme bullosa (Stevens-Johnson Syndrome); some observations on pathogenesis and on treatment with cortisone and ACTH", Postgrad Med J, 31, pp.570~574 (1995)
  12. Shetty SR, "Stevens-Johnson syndrome: a case report", J Oral Sci, 52, pp.343~346 (2000)
  13. Apajalahti S, "Prevalence of short-root anomaly in healthy young adults", Acta Odontol Scand, 60, pp.56~59 (2002)
  14. Bachot N, "Differential diagnosis of severe cutaneous drug eruptions", Am J Clin Dermatol, 4, pp.561~572 (2003)
  15. Fritsch PO, "Drug-induced Stevens-Johnson syndrome", toxic epidermal necrolysis, 2000, pp.1, 349~360
  16. Bastuji-Garin S, "Clinical classification of cases of toxic epidermal necrolysis, Stevens-Johnson syndrome, and erythema multiforme", Arch Dermatol, 129, pp.92~96 (1993)
  17. Assier H, "Erythema multiforme with mucous membrane involvement and Stevens-Johnson syndrome are clinically different disorders with distinct causes", Arch Dermatol, 131, pp.539~543 (1995)
  18. Oliveira LR, "Erythema Multiforme Minor: A Revision", American Journal of Infectious Disease, 4, pp.224~231 (2008)
  19. Del Pozzo-Magana BR, "A systematic review of treatment of drug-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in children", J Popul Ther Clin Pharmacol, 18, pp.121~133 (2011)
  20. Bachot N, "Intravenous immunoglobulin treatment for Stevens-Johnson syndrome and toxic epidermal necrolysis: a prospective noncomparative study showing no benefit on mortality or progression", Arch Dermatol, 139, pp.33~36 (2003)
  21. Huang X, "Fate of HERS during tooth root development", Dev Biol, 334, pp.22~30 (2009)
  22. Ranalli DN, "Stevens-Johnson syndrome: report of case with abnormal root development", ASDC J Dent Child, 51, pp.298~301 (1984)

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