A case of toxic epidermal necrolysis in a paediatric patient with mycoplasma pneumoniae infection
DOI:
https://doi.org/10.18203/2320-6012.ijrms20253190Keywords:
Toxic epidermal necrolysis, Stevens-Johnson syndrome, Mycoplasma pneumoniae, Paediatrics, Body surface area, Critical careAbstract
Toxic Epidermal Necrolysis (TEN) is a rare, life-endangering emergency condition with a high mortality rate. While medications are recognized as common trigger factors, infections like Mycoplasma pneumoniae are also increasingly being recognized as other potential triggers, particularly in the paediatric population. A 6-year-old boy presented with fever, sore throat and tender skin lesions that rapidly progressed from erythema, macular rash to multiple vesicles, flaccid bullae and erosion, affecting more than 70% of total body surface area. Epidermal necrolysis affects more than 30% of the total body surface area including genital, oral and conjunctival mucus membranes. A diagnosis of Toxic Epidermal Necrolysis was established. Laboratory tests confirmed Mycoplasma pneumoniae infection and a chest Х-ray revealed pneumonia. For management of TEN, IVIG, followed by Methylprednisolone pulses were in combination. This was combined with antibacterial therapy and supportive care. The patient made a complete recovery with no complications after 36 days under Intensive Care. This case underscores Mycoplasma pneumoniae as a paediatric TEN trigger. It also serves to highlight the efficacy of combined immunotherapy and multidisciplinary care and the importance of early intervention in minimizing complications, especially in such severe cases.
Metrics
References
Alajmi A, Jfri A, Gomolin A, Jafarian F. A pediatric case of Stevens-Johnson syndrome/toxic epidermal necrolysis with rapid response to intravenous cyclosporine. JAAD Case Rep. 2020;6(6):555–7. DOI: https://doi.org/10.1016/j.jdcr.2020.04.003
Del Pozzo-Magaña BR, Lazo-Langner A. Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Children: A Literature Review of Current Treatments. EMJ Dermatology. 2016;83–9. DOI: https://doi.org/10.33590/emjdermatol/10314211
Labib A, Milroy C. Toxic Epidermal Necrolysis; 2025.
Lerch M, Mainetti C, Terziroli Beretta-Piccoli B, Harr T. Current Perspectives on Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis. Clin Rev Allergy Immunol. 2018;54(1):147–76. DOI: https://doi.org/10.1007/s12016-017-8654-z
McPherson T, Exton LS, Biswas S, Creamer D, Dziewulski P, Newell L, et al. British Association of Dermatologists’ guidelines for the management of Stevens–Johnson syndrome/toxic epidermal necrolysis in children and young people, 2018. British Journal of Dermatology. 2019;181(1):37–54. DOI: https://doi.org/10.1111/bjd.17841
Heuer R, Paulmann M, Annecke T, Behr B, Boch K, Boos AM, et al. S3 guideline: Diagnosis and treatment of epidermal necrolysis (Stevens‐Johnson syndrome and toxic epidermal necrolysis) – Part 1: Diagnosis, initial management, and immunomodulating systemic therapy. JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 2024;22(10):1448–66. DOI: https://doi.org/10.1111/ddg.15515
Maity S, Banerjee I, Sinha R, Jha H, Ghosh P, Mustafi S. Nikolsky’s sign: A pathognomic boon. J Family Med Prim Care. 2020;9(2):526–30. DOI: https://doi.org/10.4103/jfmpc.jfmpc_889_19
Canhão G, Pinheiro S, Cabral L. Toxic Epidermal Necrolysis: A Clinical and Therapeutic Review. European Burn Journal. 2022;3(3):407–24. DOI: https://doi.org/10.3390/ebj3030036
Gillis NK, Hicks JK, Bell GC, Daly AJ, Kanetsky PA, McLeod HL. Incidence and Triggers of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in a Large Cancer Patient Cohort. J Invest Dermatol. 2017;137(9):2021–3. DOI: https://doi.org/10.1016/j.jid.2017.05.010
Liotti L, Caimmi S, Bottau P, Bernardini R, Cardinale F, Saretta F, et al. Clinical features, outcomes and treatment in children with drug induced Stevens-Johnson syndrome and toxic epidermal necrolysis. Acta Biomed. 2019;90(3-S):52–60.
Yang MS, Kang MG, Jung JW, Song WJ, Kang HR, Cho SH, et al. Clinical features and prognostic factors in severe cutaneous drug reactions. Int Arch Allergy Immunol. 2013;162(4):346–54. DOI: https://doi.org/10.1159/000354918
Creamer D, Walsh SA, Dziewulski P, Exton LS, Lee HY, Dart JKG, et al. U.K. guidelines for the management of Stevens–Johnson syndrome/toxic epidermal necrolysis in adults 2016. British Journal of Dermatology. 2016;174(6):1194–227. DOI: https://doi.org/10.1016/j.bjps.2016.01.034
Viard-Leveugle I, Gaide O, Jankovic D, Feldmeyer L, Kerl K, Pickard C, et al. TNF-α and IFN-γ are potential inducers of Fas-mediated keratinocyte apoptosis through activation of inducible nitric oxide synthase in toxic epidermal necrolysis. J Invest Dermatol. 2013;133(2):489–98. DOI: https://doi.org/10.1038/jid.2012.330
Lee HY, Fook-Chong S, Koh HY, Thirumoorthy T, Pang SM. Cyclosporine treatment for Stevens-Johnson syndrome/toxic epidermal necrolysis: Retrospective analysis of a cohort treated in a specialized referral center. J Am Acad Dermatol. 2017;76(1):106–13. DOI: https://doi.org/10.1016/j.jaad.2016.07.048
Zimmermann S, Sekula P, Venhoff M, Motschall E, Knaus J, Schumacher M, et al. Systemic Immunomodulating Therapies for Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis: A Systematic Review and Meta-analysis. JAMA Dermatol. 2017;153(6):514–22. DOI: https://doi.org/10.1001/jamadermatol.2016.5668
Frantz R, Huang S, Are A, Motaparthi K. Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis: A Review of Diagnosis and Management. Medicina (B Aires). 2021;57(9):895. DOI: https://doi.org/10.3390/medicina57090895
French LE. Toxic Epidermal Necrolysis and Stevens Johnson Syndrome: Our Current Understanding. Allergology International. 2006;55(1):9–16. DOI: https://doi.org/10.2332/allergolint.55.9
Silversides JA, Lappin E, Ferguson AJ. Staphylococcal toxic shock syndrome: mechanisms and management. Curr Infect Dis Rep. 2010;12(5):392–400. DOI: https://doi.org/10.1007/s11908-010-0119-y
De A, Rajagopalan M, Sarda A, Das S, Biswas P. Drug Reaction with Eosinophilia and Systemic Symptoms: An Update and Review of Recent Literature. Indian J Dermatol. 2018;63(1):30–40. DOI: https://doi.org/10.4103/ijd.IJD_582_17