Cohen Philip R
Philip R Cohen, Department of Dermatology, University of California San Diego, San Diego, CA 92131-3643, United States.
World J Clin Cases. 2016 Dec 16;4(12):390-400. doi: 10.12998/wjcc.v4.i12.390.
Drug-induced reticulate hyperpigmentation is uncommon. Including the patient described in this report, chemotherapy-associated reticulate hyperpigmentation has only been described in ten individuals. This paper describes the features of a woman with recurrent and metastatic breast cancer who developed paclitaxel-induced reticulate hyperpigmentation and reviews the characteristics of other oncology patients who developed reticulate hyperpigmentation from their antineoplastic treatment. A 55-year-old Taiwanese woman who developed reticulate hyperpigmentation on her abdomen, back and extremities after receiving her initial treatment for metastatic breast cancer with paclitaxel is described. The hyperpigmentation became darker with each subsequent administration of paclitaxel. The drug was discontinued after five courses and the pigment faded within two months. PubMed was searched with the key words: Breast, cancer, chemotherapy, hyperpigmentation, neoplasm, reticulate, tumor, paclitaxel, taxol. The papers generated by the search, and their references, were reviewed. Chemotherapy-induced reticulate hyperpigmentation has been described in four men and six women. Bleomycin, cytoxan, 5-fluorouracil, idarubacin, and paclitaxel caused the hyperpigmentation. The hyperpigmentation faded in 83% of the patients between two to six months after the associated antineoplastic agent was discontinued. In conclusion, chemotherapy-induced reticulate hyperpigmentation is a rare reaction that may occur during treatment with various antineoplastic agents. The hyperpigmentation fades in most individuals once the treatment is discontinued. Therefore, cancer treatment with the associated drug can be continued in patients who experience this cutaneous adverse event.
药物性网状色素沉着并不常见。包括本报告中描述的患者在内,与化疗相关的网状色素沉着仅在10例患者中被描述过。本文描述了一名患有复发性和转移性乳腺癌的女性出现紫杉醇诱导的网状色素沉着的特征,并回顾了其他因抗肿瘤治疗而出现网状色素沉着的肿瘤患者的特点。本文描述了一名55岁的台湾女性,她在接受紫杉醇治疗转移性乳腺癌的初始治疗后,腹部、背部和四肢出现了网状色素沉着。每次后续使用紫杉醇后,色素沉着都会加深。五个疗程后停用该药物,色素在两个月内消退。使用关键词“乳腺、癌症、化疗、色素沉着、肿瘤、网状、肿瘤、紫杉醇、泰素”在PubMed上进行搜索。对搜索生成的论文及其参考文献进行了综述。化疗诱导的网状色素沉着在4名男性和6名女性中被描述过。博来霉素、环磷酰胺、5-氟尿嘧啶、伊达比星和紫杉醇导致了色素沉着。在停用相关抗肿瘤药物后的两到六个月内,83%的患者色素沉着消退。总之,化疗诱导的网状色素沉着是一种罕见的反应,可能在使用各种抗肿瘤药物治疗期间发生。一旦停止治疗,大多数人的色素沉着会消退。因此,经历这种皮肤不良事件的患者可以继续使用相关药物进行癌症治疗。