Abstract
Stevens-Johnson syndrome is a life-threatening, immune-mediated, acute inflammatory disorder of the mucocutaneous membranes. It affects people of almost any age and has a high mortality and morbidity rate. Therefore, histopathological confirmation of the diagnosis is essential. Ocular involvement occurs in more than 50% of the affected patients. Here, we report a case of Stevens-Johnson syndrome with ocular involvement in a 10-year-old boy suffering from pain, burning, stinging, and decreased vision in both eyes for over 2 years. Histopathological findings were consistent with the changes due to the syndrome. Stevens-Johnson syndrome affects various mucous membranes along with the skin. Ocular involvement may manifest both acutely and chronically and causes morbidities. A careful clinical and histopathologic examination is required in order to give the correct diagnosis.
Similar content being viewed by others
Data Availability
Not applicable.
Code Availability
Not applicable.
References
Pereira FA, Mudgil AV, Rosmarin DM. Toxic epidermal necrolysis. J Am Acad Derm. 2007;56:181–200.
Ferrandiz-Pulido C, Garcia-Patos V. A review of causes of Stevens-Johnson syndrome and toxic epidermal necrolysis in children. Arch Dis Child. 2013;98(12):998–1003.
Sotozono C, Ang LP, Koizumi N, et al. New grading system for the evaluation of chronic ocular manifestations in patients with Stevens-Johnson syndrome. Ophthalmology. 2007;114:1294–302.
Levi N, Bastuji-Garin S, Mockenhaupt M, et al. Medications as risk factors of Stevens-Johnson syndrome and toxic epidermal necrolysis in children: a pooled analysis. Pediatrics. 2009;123:297–304.
Dodiuk-Gad RP, Chung WH, Valeyrie-Allanore L, Shear NH. Stevens-Johnson syndrome and toxic epidermal necrolysis: an update. Am J Clin Dermatol. 2015;16(6):475–93.
Chow LLW, Shih KC, Chan JCY, Lai JSM, Ng ALK. Comparison of the acute ocular manifestations of Stevens-Johnson syndrome and toxic epidermal necrolysis in Chinese eyes: a 15-year retrospective study. BMC Ophthalmol. 2017;17(1):65.
Wetter DA, Camilleri MJ. Clinical, etiologic, and histopathologic features of Stevens-Johnson syndrome during an 8-year period at Mayo Clinic. Mayo Clin Proc. 2010;85(2):131–8.
Hazin R, Ibrahimi OA, Hazin MI, Kimyai-Asadi A. Stevens-Johnson syndrome: pathogenesis, diagnosis, and management. Ann Medicine. 2008;40:129–38.
Chang YS, Huang FC, Tseng SH, Hsu CK, Ho CL, Sheu HM. Erythema multiforme, Stevens-Johnson syndrome, and toxic epidermal necrolysis: acute ocular manifestations, causes, and management. Cornea. 2007;26(2):123–9.
Swamynathan SK, Wells A. Conjunctival goblet cells: ocular surface functions, disorders that affect them, and the potential for their regeneration [published correction appears in Ocul Surf. 2020 Feb 28;:]. Ocul Surf. 2020;18(1):19–26.
López-García JS, Rivas Jara L, García-Lozano CI, Conesa E, de Juan IE, Murube del Castillo J. Ocular features and histopathologic changes during follow-up of toxic epidermal necrolysis. Ophthalmology. 2011;118(2):265–71.
Ueta M. Pathogenesis of Stevens-Johnson syndrome/toxic epidermal necrolysis with severe ocular complications. Front Med (Lausanne). 2021;8: 651247.
Ueta M. Findings by an ınternational collaboration on SJS/TEN with severe ocular complications. Front Med (Lausanne). 2021;8: 649661.
Author information
Authors and Affiliations
Contributions
EG contributed to the literature review and manuscript preparation. EO contributed to the diagnosis, manuscript preparation, and editing.
Corresponding author
Ethics declarations
Ethical Approval
Not applicable.
Informed Consent to Participate
Not applicable.
Informed Consent to Publication
A written informed consent form was obtained from the parents.
Conflict of Interest
The authors declare no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
This article is part of the Topical Collection on Medicine
Rights and permissions
About this article
Cite this article
Gun, E., Ozer, E. Corneal Histopathology in Stevens-Johnson Syndrome: A Case Report and Review of Literature. SN Compr. Clin. Med. 4, 122 (2022). https://doi.org/10.1007/s42399-022-01201-5
Accepted:
Published:
DOI: https://doi.org/10.1007/s42399-022-01201-5