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一种丝裂原活化蛋白激酶激酶抑制剂在转移性恶性黑色素瘤中诱发了伴有水肿的复合性皮肤毒性。

A mitogen-activated protein kinase kinase inhibitor induced compound skin toxicity with oedema in metastatic malignant melanoma.

作者信息

Thomas C L, Mortimer P S, Larkin J M, Basu T N, Gore M E, Fearfield L

机构信息

Department of Dermatology, St George's Hospital, London, UK.

Department of Dermatology, The Royal Marsden Hospital, London, UK.

出版信息

Clin Exp Dermatol. 2016 Apr;41(3):267-71. doi: 10.1111/ced.12722. Epub 2015 Sep 28.

Abstract

We report three cases of skin toxicity associated with oral mitogen-activated protein kinase kinase (MEK) inhibitor treatment for metastatic malignant melanoma (MM). All three patients developed oedema, and a single patient experienced eyelash trichomegaly. This is the first known report of eyelash trichomegaly secondary to MEK inhibitor use. We also discuss possible mechanisms for MEK inhibitor-associated oedema development. This series supports the role of the dermatologist in the screening and management of patients in the rapidly developing oncology setting, as new targeted agents can give rise to marked skin toxicity.

摘要

我们报告了3例与口服丝裂原活化蛋白激酶激酶(MEK)抑制剂治疗转移性恶性黑色素瘤(MM)相关的皮肤毒性病例。所有3例患者均出现水肿,1例患者出现睫毛粗长。这是首例关于使用MEK抑制剂继发睫毛粗长的已知报告。我们还讨论了MEK抑制剂相关水肿发生的可能机制。该系列病例支持皮肤科医生在快速发展的肿瘤学环境中对患者进行筛查和管理的作用,因为新的靶向药物可能会引起明显的皮肤毒性。

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