Ann Dermatol. 2021 Dec;33(6):584-586. English.
Published online Nov 04, 2021.
Copyright © 2021 The Korean Dermatological Association and The Korean Society for Investigative Dermatology
Brief Communication

Abrupt Development of Esophageal Candidiasis after Secukinumab Treatment in a Psoriatic Patient

Hyun Jin Kang, Ju Hee Han, Chul Hwan Bang and Tae-Yoon Kim
    • Department of Dermatology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Received April 04, 2020; Revised June 29, 2020; Accepted July 01, 2020.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Dear Editor:

A 61-year-old male presented with a 40-year history of psoriasis on the whole body. He had previously been treated with methotrexate and topical betamethasone dipropionate/calcipotriol gel for two years in the local clinic. His medical history included diabetes mellitus (DM) and hypertension. Physical examination revealed multiple, erythematous scaly papules and plaques on the trunk and extremities (Fig. 1). Histopathologic findings showed parakeratosis, hypogranulosis and regular acanthosis with rete ridge elongation in the epidermis. Dilated capillaries and mild perivascular lymphohistiocytic infiltration were observed in the upper dermis (Fig. 2A). Routine laboratory examination showed no specific findings. He was treated with secukinumab 300 mg injected subcutaneously according to the standard schedule (weeks 0, 1, 2, 3, and 4, and every 4 weeks thereafter). After the fourth injection, dysphagia, odynophagia and abdominal discomfort developed. Esophagogastroduodenoscopy (EGD) demonstrated multiple whitish to yellowish plaques on the esophageal mucosal surface (Fig. 2B). Fungus culture and identification revealed Candida albicans. Under the diagnosis of esophageal candidiasis, he was treated with fluconazole 200 mg/day for seven days. Afterwards, the symptoms improved, and subsequent EGD showed resolution of candidiasis. Currently, the patient has been treated with guselkumab 100 mg for three months, and no recurrence of candidiasis has been observed.

Fig. 1
Multiple, erythematous papules and plaques with scales on the trunk and extremities. We received the patient's consent form about publishing all photographic materials.

Fig. 2
(A) Histopathologic findings showed parakeratosis, hypogranulosis and regular acanthosis with elongation of rete ridges in the epidermis. Dilated capillaries and mild perivascular lymphohistiocytic infiltration were observed in the upper dermis (H&E, ×100). (B) Esophagogastroduodenoscopy revealed diffuse whitish to yellowish patches on the mucosal surface of esophagus.

Secukinumab is an anti-interleukin (IL) 17A monoclonal antibody used for the treatment of moderate-to-severe plaque psoriasis and psoriatic arthritis1, 2. However, since IL-17A plays an essential role in immunological protection against various infections, inhibition of IL-17A can increase the susceptibility of patients to Candida infections2. According to the systematic review performed by Saunte et al.2, there was an increased incidence of Candida infections in patients treated with anti-IL-17A agents compared to placebo. Most cases involved orogenital candidiasis (26.5%), and esophageal involvement was relatively uncommon (2.4%). During the average follow-up period of 12 to 52 weeks, esophageal candidiasis occurred at least after eight weeks of injection, and there was no reported case that occurred in less than a month2.

Herein, we report an unusual case of a patient with psoriasis who developed esophageal candidiasis three weeks after treatment with secukinumab. He denied any history of candidiasis prior to the treatment. Since patients with underlying diseases such as DM, AIDS, or hematologic malignancies are more susceptible to infections3, our patient's underlying DM may have acted as a predisposing factor to such an early infection.

Thus, this case is worth reporting in three points. Firstly, it suggests that certain patients with underlying immune dysregulation can have Candida infections more abruptly than healthy individuals. Especially, since IL-17A plays a key role in host defense, clinicians should keep vigilance to the potential mucocutaneous infections when prescribing secukinumab4. Secondly, EGD must be used to evaluate esophageal candidiasis when the characteristic symptoms such as dysphagia, odynophagia, and abdominal discomfort occur. Lastly, not only clinicians, but also patients should be educated on the symptoms of Candida infections and advised to seek care when necessary3. Upon early diagnosis and appropriate antifungal treatments, most Candida infections are resolved, and biologic treatments can be continued without serious complications.

Notes

CONFLICTS OF INTEREST:The authors have nothing to disclose.

FUNDING SOURCE:None.

References

    1. Ha DL, Kim WI, Yang MY, Lee WK, Kim T, Park S, et al. Efficacy and safety of secukinumab for the treatment of moderate to severe psoriasis in Korea. Korean J Dermatol 2019;57:9–14.
    1. Saunte DM, Mrowietz U, Puig L, Zachariae C. Candida infections in patients with psoriasis and psoriatic arthritis treated with interleukin-17 inhibitors and their practical management. Br J Dermatol 2017;177:47–62.
    1. Vallabhaneni S, Chiller TM. Fungal infections and new biologic therapies. Curr Rheumatol Rep 2016;18:29
    1. Langley RG, Elewski BE, Lebwohl M, Reich K, Griffiths CE, Papp K, et al. Secukinumab in plaque psoriasis--results of two phase 3 trials. N Engl J Med 2014;371:326–338.

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