JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY | 卷:62 |
Chronic phototoxicity and aggressive squamous cell carcinoma of the skin in children and adults during treatment with voriconazole | |
Article | |
Cowen, Edward W.1  Nguyen, Josephine C.1  Miller, Daniel D.2  McShane, Diana3  Arron, Sarah T.2  Prose, Neil S.3  Turner, Maria L.1  Fox, Lindy P.2  | |
[1] NCI, Dermatol Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA | |
[2] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA | |
[3] Duke Univ, Dept Dermatol, Durham, NC 27706 USA | |
关键词: fungal infection; immunosuppression; photoaging; photosensitivity; phototoxicity; squamous cell carcinoma; voriconazole; | |
DOI : 10.1016/j.jaad.2009.09.033 | |
来源: Elsevier | |
【 摘 要 】
Background. Voriconazole is a broad-spectrum antifungal agent associated with photosensitivity and accelerated photoaging. A possible link with aggressive squamous cell carcinoma (SCC) has also been reported. Objective: We sought to determine the incidence and frequency of cutaneous SCC among patients undergoing long-term treatment with voriconazole who also manifest features of chronic phototoxicity. Methods: We conducted a retrospective review of patients who developed one or more squamous cell neoplasms during long-term treatment with voriconazole at 3 academic dermatology centers. Results: A total of 51 cutaneous SCC were identified in 8 patients (median age 34.5 years, range 9-54) treated with chronic voriconazole (median duration 46.5 months, range 13-60). Underlying diagnoses included graft-versus-host disease, HIV, and Wegener granulomatosis. Signs of chronic phototoxicity and accelerated photoaging included erythema, actinic keratoses, and lentigo formation. Limitations: The retrospective nature of the study cannot determine the true population risk of SCC associated with voriconazole therapy. A prospective cohort study is needed. Conclusion: A high index of suspicion for photosensitivity and SCC may be warranted with chronic voriconazole use when used in the setting of concurrent immunosuppression. (J Am Acad Dermatol 2010;62:31-7.)
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