Case report: Managing pemphigus foliaceus using apremilast without systemic glucocorticosteroids or immunosuppressive agents.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2024
Historique:
received: 27 03 2024
accepted: 15 07 2024
medline: 14 8 2024
pubmed: 14 8 2024
entrez: 14 8 2024
Statut: epublish

Résumé

Pemphigus foliaceus (PF) is a superficial form of pemphigus. Treatment options for PF resemble pemphigus vulgaris, including glucocorticosteroids, immunosuppressive agents and rituximab et al. These treatment approaches can effectively improve the condition but may also be accompanied by high risks of side effects. Therefore, it is crucial to find a safe and effective treatment options for patients with PF. It will not only benefit/be necessary for patients who refuse glucocorticosteroids or immunosuppressive agents treatments, but also for patients who cannot be treated with glucocorticosteroids or immunosuppressive agents. Herein, we reported a case of PF that was treated with apremilast without systemic glucocorticosteroids or immunosuppressive agents. A 54-year-old woman presented with itchy erythema and erosions on the trunk for more than 1 month. The patient applied mometasonefuroate cream without improvement for a duration of two weeks. The past history of diabetes mellitus and atrophic gastritis was reported. Physical examination revealed scattered erythematous macules and erosions on the trunk. No mucosal involvement was observed. The condition was assessed by the pemphigus disease area index and numerical rating scale, with baseline scores of 7 and 8, respectively. Histopathological examination showed acantholysis and intraepithelial blister. Direct immunofluorescence revealed the presence of IgG and Complement 3 deposition between the acanthocytes with the reticular distribution. Based on enzyme-linked immunosorbent assay results, the levels of Dsg1 and Dsg3 antibodies were 28.18 and 0.26 kU/L respectively. The diagnosis of PF was made. This patient was successfully treated with apremilast without systemic glucocorticosteroids or immunosuppressive agents. The patient has continued with apremilast 30mg once daily for maintenance and no adverse events related to apremilast such as gastrointestinal side effects were observed during the 9-month follow-up period. In conclusion, apremilast therapy without systemic glucocorticosteroids nor immunosuppressive agents might provide an effective alternative to management of mild PF without obvious side effect.

Identifiants

pubmed: 39139566
doi: 10.3389/fimmu.2024.1408116
pmc: PMC11319141
doi:

Substances chimiques

apremilast UP7QBP99PN
Thalidomide 4Z8R6ORS6L
Immunosuppressive Agents 0
Glucocorticoids 0
Anti-Inflammatory Agents, Non-Steroidal 0

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1408116

Informations de copyright

Copyright © 2024 Zhang, Yu, Wan, Chen and Chen.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Quanhong Zhang (Q)

Department of Dermatology, Wuhan No.1 Hospital, Wuhan, China.
Department of Dermatology, Traditional Chinese and Western Medicine Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Lang Yu (L)

Department of Dermatology, Wuhan No.1 Hospital, Wuhan, China.
Jianghan University School of Medicine, Wuhan, China.

Li Wan (L)

Dermatology Hospital of Southern Medical University, Guangzhou, China.

Liuqing Chen (L)

Department of Dermatology, Wuhan No.1 Hospital, Wuhan, China.
Hubei Province & Key Laboratory of Skin Infection And Immunity, Wuhan, China.

Jinbo Chen (J)

Department of Dermatology, Wuhan No.1 Hospital, Wuhan, China.
Hubei Province & Key Laboratory of Skin Infection And Immunity, Wuhan, China.

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Classifications MeSH