Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2017 Jul 1;153(7):694-697.
doi: 10.1001/jamadermatol.2017.0989.

Eruptive Keratoacanthomas Associated With Pembrolizumab Therapy

Affiliations
Case Reports

Eruptive Keratoacanthomas Associated With Pembrolizumab Therapy

Azael Freites-Martinez et al. JAMA Dermatol. .

Abstract

Importance: To our knowledge, there have been no previous reports of eruptive keratoacanthomas (KAs) in patients receiving pembrolizumab.

Objective: To report the cases of 3 consecutive patients with pembrolizumab-induced eruptive KAs and their management.

Design, setting, and participants: Case report study of 3 patients from 2 centers with pembrolizumab-treated cancer who all developed eruptive KAs.

Interventions: All 3 patients had AK treatment with clobetasol ointment and intralesional triamcinolone; 2 patients also underwent open superficial cryosurgery.

Results: Three consecutive patients with cancer, 2 men and 1 woman (median age, 83 years; range 77-91 years), experienced pembrolizumab-associated eruptive KAs. All patients presented with a sudden onset of multiple lesions on sun-exposed areas of their extremities after a median of 13 months (range, 4-18 months) of pembrolizumab therapy. On lesional biopsy, a lichenoid infiltrate was observed in the underlying dermis, predominantly composed of CD3+ T cells, scattered CD20+ B cells, and relatively few PD-1+ (programmed cell death 1-positive) T cells, an immunophenotypic pattern also observed in other cases of anti-PD-1-induced lichenoid dermatitis. Patients were treated with clobetasol ointment and intralesional triamcinolone, alone or in combination with open superficial cryosurgery. All KAs resolved in all patients, and no new lesions occurred during close follow-up. Pembrolizumab treatment was continued without disruption in all 3 cases, and all patients had complete responses of their primary cancers.

Conclusions and relevance: Pembrolizumab is used in advanced melanoma, advanced non-small-cell lung cancer, and in head and neck cancer. A variety of dermatologic immune-related adverse events including maculopapular eruption, lichenoid reactions, pruritus, and vitiligo have been described. This case series demonstrates that pembrolizumab therapy may also be associated with eruptive KAs with characteristic dermal inflammation, which improved with corticosteroid treatment (topical and intralesional) alone or in combination with cryosurgery, allowing patients to continue therapy with pembrolizumab.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest Disclosures: None reported.

Figures

Figure 1.
Figure 1.. Clinical Features Before and After Therapy With Clobetasol Ointment and Intralesional Triamcinolone Only (Patient 3)
A, Multiple erythematous, hyperkeratotic nodules and papules on dorsal hand surface. B, Therapy results 5 months after treatment.
Figure 2.
Figure 2.. Hematoxylin-Eosin Biopsy Sections Showing a Multiloculated, Crateriform, Keratin-Filled Atypical Squamoproliferative Lesion
A, Large keratinocytes with glassy-appearing, eosinophilic cytoplasm and minimal cytologic atypia. B, Higher magnification.

References

    1. Kwiek B, Schwartz RA. Keratoacanthoma (KA): an update and review. J Am Acad Dermatol. 2016;74(6):1220-1233. - PubMed
    1. Tidwell WJ, Malone J, Callen JP. Eruptive keratoacanthomas associated with leflunomide. JAMA Dermatol. 2016;152(1):105-106. - PubMed
    1. Lacouture ME, Morris JC, Lawrence DP, et al. Cutaneous keratoacanthomas/squamous cell carcinomas associated with neutralization of transforming growth factor β by the monoclonal antibody fresolimumab (GC1008). Cancer Immunol Immunother. 2015;64(4):437-446. - PMC - PubMed
    1. Aasi S, Silkiss R, Tang JY, et al. New onset of keratoacanthomas after vismodegib treatment for locally advanced basal cell carcinomas: a report of 2 cases. JAMA Dermatol. 2013;149(2):242-243. - PMC - PubMed
    1. Belum VR, Rosen AC, Jaimes N, et al. Clinico-morphological features of BRAF inhibition-induced proliferative skin lesions in cancer patients. Cancer. 2015;121(1):60-68. - PubMed

Publication types

MeSH terms