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应用5%咪喹莫特软膏单一治疗皮肤原位鳞状细胞癌(鲍温病):一项随机、双盲、安慰剂对照试验 被引量:1
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作者 Patel G.K. Goodwin R. +1 位作者 Chawla M. 吴佳纹 《世界核心医学期刊文摘(皮肤病学分册)》 2006年第8期54-55,共2页
Background: We conducted a double-blind, placebo-controlled, randomized trial to evaluate the preliminary efficacy and safety of imiquimod 5% cream treatment for cutaneous squamous cell carcinoma (SCC) in situ. Method... Background: We conducted a double-blind, placebo-controlled, randomized trial to evaluate the preliminary efficacy and safety of imiquimod 5% cream treatment for cutaneous squamous cell carcinoma (SCC) in situ. Methods: In all, 31 patients with biopsy-proven cutaneous SCC in situ were randomly assigned to placebo (vehicle) (n = 16) or imiquimod 5% cream (n = 15) daily for 16 weeks. Patients were assessed at week 28 for the primary end point, resolution of cutaneous SCC in situ. Results: Of the 31 patients enrolled, 3 dropped out. Intention-to-treat analysis revealed 11 of the 15 patients (73% ) in the imiquimod group achieved resolution of cutaneous SCC in situ, with no relapse during the 9-month follow-up period; none in the placebo group achieved resolution (P < .001). Imiquimod 5% cream was generally well tolerated and there were no serious adverse events. Limitations: Topical imiquimod 5% cream has proven to be an effective treatment for cutaneous SCC in situ. However, studies to define the ideal dosing regimen and cost-effectiveness are required before it can be accepted as a recognized therapy. Conclusions: In this controlled trial, patients with cutaneous SCC in situ receiving topical imiquimod 5% cream as monotherapy experienced a high degree of clinical benefit compared with placebo. 展开更多
关键词 5%咪喹莫特 鳞状细胞癌 对照试验 随机分配 单一治疗 安慰剂 原位 皮肤 软膏 双盲
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1例15岁男性内瑟顿综合征患儿在心脏移植后发生原发性皮肤CD30+T细胞淋巴组织增生异常
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作者 Katugampola R.P. Finlay A.Y. +1 位作者 Harper J.I. 潘敏 《世界核心医学期刊文摘(皮肤病学分册)》 2006年第2期39-39,共1页
Primary cutaneous T- cell lymphoproliferative disorders (PCTCLDs) are uncommon in organ transplant recipients. CD30+ PCTCLDs are rare in children and have not previously been reported following organ transplantation. ... Primary cutaneous T- cell lymphoproliferative disorders (PCTCLDs) are uncommon in organ transplant recipients. CD30+ PCTCLDs are rare in children and have not previously been reported following organ transplantation. We report a 15- yearold boy with Netherton’ s syndrome who developed CD30+ PCTCLD 6 years following a cardiac transplantation. 展开更多
关键词 CD30+T细胞 心脏移植 淋巴组织增生 器官移植患者 器官移植受者
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