Salopek Thomas G
Division of Dermatology, Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Case Rep Dermatol. 2017 Aug 3;9(2):108-111. doi: 10.1159/000478898. eCollection 2017 May-Aug.
This is a report on a 32-year-old man with a history of two previous melanomas with concurrent plaque-type psoriasis. His history dates to 2009, when he was diagnosed with his first melanoma on the right occiput, Clark's level IV, tumor thickness 1.53 mm, nonulcerated, mitotic index 1/mm. He subsequently developed nodal recurrence after an initial negative sentinel lymph node biopsy and was treated with complete lymph node dissection. In 2012, he was diagnosed with a second primary melanoma on the right upper chest, Clark's level IV, tumor thickness 0.9 mm, nonulcerated, mitotic index 3/mm. Due to worsening longstanding plaque-type psoriasis in 2015 he was placed on apremilast, with a dramatic improvement in his psoriasis within 4 months of starting therapy. Shortly thereafter the patient developed multiple blue-colored skin papules on the scalp near his first melanoma and on the trunk and upper limbs that on biopsy proved to be due to cutaneous metastasis of melanoma. The patient discontinued the apremilast as there was a concern that his tumor had recurred because of the drug. Apremilast is a phosphodiesterase-4 inhibitor that impairs the innate immune system, which mediates cancer immunosurveillance. It is postulated that the use of apremilast in our patient resulted in impaired cancer immunosurveillance and led to a recurrence of his melanoma. Although one cannot exclude the possibility of coincidental recurrence of an already metastatic melanoma (to the lymph nodes), caution should be exercised when considering apremilast in the context of patients with known malignancy, in particular melanoma.
这是一份关于一名32岁男性的报告,他有两次黑色素瘤病史,同时患有斑块型银屑病。他的病史可追溯到2009年,当时他在右枕部被诊断出患有首例黑色素瘤,Clark分级为IV级,肿瘤厚度1.53mm,无溃疡,有丝分裂指数为1/mm。他在最初前哨淋巴结活检为阴性后出现了淋巴结复发,并接受了根治性淋巴结清扫术。2012年,他在右上胸部被诊断出患有第二原发性黑色素瘤,Clark分级为IV级,肿瘤厚度0.9mm,无溃疡,有丝分裂指数为3/mm。由于其长期存在的斑块型银屑病在2015年病情恶化,他开始使用阿普司特治疗,在开始治疗后的4个月内,他的银屑病有了显著改善。此后不久,患者在其首例黑色素瘤附近的头皮以及躯干和上肢出现了多个蓝色皮肤丘疹,活检证实这些丘疹是由黑色素瘤的皮肤转移引起的。由于担心肿瘤因该药物复发,患者停用了阿普司特。阿普司特是一种磷酸二酯酶-4抑制剂,会损害介导癌症免疫监视的先天免疫系统。据推测,我们的患者使用阿普司特导致癌症免疫监视受损,进而导致他的黑色素瘤复发。虽然不能排除已经发生转移的黑色素瘤(至淋巴结)巧合复发的可能性,但在已知患有恶性肿瘤,尤其是黑色素瘤的患者中考虑使用阿普司特时应谨慎。