日本性感染症学会誌 Journal of Japanese Society for Sexually Transmitted Infections

Online ISSN: 2434-2505 Print ISSN: 0917-0324
日本性感染症学会 Japanese Society for Sexually Transmitted Infections
〒162-0801東京都新宿区山吹町358-5アカデミーセンター Japanese Society for Sexually Transmitted Infections Academy Center, 358-5 Yamabuki-cho, Shinju-ku, Tokyo 162-0801, Japan
Japanese Journal of Sexually Transmitted Infections 31(1): 113-116 (2020)
doi:10.24775/jjsti.C-2020-0002

症例報告症例報告

セツキシマブ投与中に多発潰瘍を生じた非典型的な臀部ヘルペス性潰瘍の1例A case of non-typical herpetic ulcer of the buttocks causing the repeated recurrence of an ulcer during chemotherapy

愛知医科大学皮膚科学教室Department of Dermatology, Aichi Medical University School of Medicine

受付日:2020年5月15日Received: May 15, 2020
受理日:2020年8月12日Accepted: August 12, 2020
発行日:2020年10月6日Published: October 6, 2020
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An 80-year-old Japanese male presented to our department with multiple ulcerous lesions on the buttocks. Prior to the appearance of the lesions on the buttocks, he had been on cetuximab for four months for the treatment of the recurrence of a rectal cancer. We supposed that the lesions were caused by cetuximab, therefore, topical corticosteroid was applied to the lesion. However, there was no improvement. We performed a skin biopsy and the histopathological findings showed multinucleated keratinocytes with inclusion bodies in the epidermis associated with infiltration of lymphoid cells in the dermis. A swab sample of the biopsy of the lesion using the loop-mediated isothermal amplification, was positive for herpes simplex virus-2 DNA. Treatment with cetuximab was discontinued and oral valaciclovir (500 mg twice daily) was administrated for 14 days. The skin lesions of the patient had healed with pigmentation 45 days after the initiation of this treatment. Treatment with cetuximab was then restarted; however, a few months later, the lesions flared up. Oral valaciclovir (500 mg twice daily) was then administrated for 14 days followed by suppressive therapy with oral valaciclovir (500 mg daily). No recurrence was observed after the suppressive therapy.

Key words: non-typical herpes simplex; molecularly targeted drugs; cetuximab

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