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伊马替尼诱发全身性色素减退及现有获得性皮肤黑素增多症进展的病例系列

A case series of imatinib-induced generalized hypopigmentation and progression of existing acquired dermal melanocytosis.

作者信息

Kok Wai Leong, Chen Qiping, Lee Siong See Joyce, Chua Sze Hon, Ng See Ket

机构信息

a National Skin Center , Singapore.

出版信息

J Dermatolog Treat. 2017 Dec;28(8):762-763. doi: 10.1080/09546634.2017.1328099. Epub 2017 May 16.

Abstract

Imatinib mesylate is a tyrosine kinase inhibitor used in the treatment of oncological conditions, including chronic myeloid leukemia and gastrointestinal stromal tumors. The most frequent dermatological side effect reported is pigmentary abnormalities. We report a case series of three Asian Chinese females with preexisting acquired dermal melanocytosis that progressed after initiation of imatinib treatment, and concurrently developed generalized hypopigmentation of the skin. All three patients had similar histological findings on skin biopsy. It is postulated that the KIT/SCF pathway has a central role in the pathogenetic mechanism. Therefore, it is important for physicians to be aware of this potential side effect of paradoxical pigmentation in patients treated with imatinib.

摘要

甲磺酸伊马替尼是一种酪氨酸激酶抑制剂,用于治疗包括慢性粒细胞白血病和胃肠道间质瘤在内的肿瘤疾病。报道的最常见皮肤副作用是色素异常。我们报告了一例系列病例,三名患有先天性获得性皮肤黑素细胞增多症的华裔亚洲女性在开始伊马替尼治疗后病情进展,同时出现皮肤广泛性色素减退。所有三名患者的皮肤活检组织学结果相似。据推测,KIT/SCF通路在发病机制中起核心作用。因此,对于医生来说,了解接受伊马替尼治疗的患者出现矛盾性色素沉着这一潜在副作用很重要。

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引用本文的文献

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