Herpetic gingivostomatitis mimicking Stevens-Johnson syndrome in an immunosuppressed adolescent with idiopathic chorioretinitis

We present the case of an 18-year-old male with bilateral idiopathic chorioretinitis maintained on immunosuppressive therapy with prednisone, adalimumab, and mycophenolate mofetil, who developed ulcers and bleeding of the lip mucosa after taking nonsteroidal anti-inflammatory drugs (NSAIDs) and amoxicillin/clavulanate for a suspected ear infection. The clinical presentation initially mimicked Stevens-Johnson syndrome (SJS), but further evaluation confirmed the diagnosis of herpetic gingivostomatitis. This case highlights the diagnostic challenges in differentiating between drug eruptions and infectious etiologies in immunosuppressed patients. Despite its severity, prompt recognition and antiviral therapy can lead to full recovery.

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Journal
IDCases
Published
2025-01-01
DOI
https://doi.org/10.1016/j.idcr.2025.e02321
Primary Topic
Drug-Induced Adverse Reactions
Type
article
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article

Herpetic gingivostomatitis mimicking Stevens-Johnson syndrome in an immunosuppressed adolescent with idiopathic chorioretinitis

Negin Yavari, Zheng Xian Thng, Jia‐Horung Hung, Aim-On Saengsirinavin et al.
IDCases
Drug-Induced Adverse Reactions
article

Herpetic gingivostomatitis mimicking Stevens-Johnson syndrome in an immunosuppressed adolescent with idiopathic chorioretinitis

Negin Yavari, Zheng Xian Thng, Jia‐Horung Hung, Aim-On Saengsirinavin, Christopher Or, Ngoc Trong Tuong Than, Azadeh Mobasserian, C. M. John, Çigdem Yaşar, Amir Akhavanrezayat, Xiaoyan Zhang, Quan Dong Nguyen, Chaw-Ning Lee, Osama Elaraby, Dalia El Feky, Frances Andrea Añover
article en

Abstract

We present the case of an 18-year-old male with bilateral idiopathic chorioretinitis maintained on immunosuppressive therapy with prednisone, adalimumab, and mycophenolate mofetil, who developed ulcers and bleeding of the lip mucosa after taking nonsteroidal anti-inflammatory drugs (NSAIDs) and amoxicillin/clavulanate for a suspected ear infection. The clinical presentation initially mimicked Stevens-Johnson syndrome (SJS), but further evaluation confirmed the diagnosis of herpetic gingivostomatitis. This case highlights the diagnostic challenges in differentiating between drug eruptions and infectious etiologies in immunosuppressed patients. Despite its severity, prompt recognition and antiviral therapy can lead to full recovery.

IDCasesVol. 41
National University of Singapore (SG), Palo Alto University (US), Tanta University (EG), Tan Tock Seng Hospital (SG), Smith-Kettlewell Eye Research Institute (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 80%
Drug-Induced Adverse Reactions
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