首页> 外文期刊>International journal of dermatology >Imatinib‐induced diffuse hyperpigmentation of the oral mucosa, the skin, and the nails in a patient affected by chronic myeloid leukemia: report of a case and review of the literature
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Imatinib‐induced diffuse hyperpigmentation of the oral mucosa, the skin, and the nails in a patient affected by chronic myeloid leukemia: report of a case and review of the literature

机译:受慢性髓性白血病影响的患者中口腔粘膜,皮肤和钉子的脱氨酰胺弥漫性超沉膜:对文献的报告和审查

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Abstract Background Imatinib mesylate is a tyrosine‐kinase inhibitor used as the first‐line treatment in chronic myeloid leukemia patients, but it is also indicated for other hematological diseases and solid tumors. Imatinib treatment is often associated with hypopigmentation, but only a few cases of hyperpigmentation are described in literature. Methods We are reporting the first case of imatinib‐related hyperpigmentation involving the oral mucosa, skin, and nails in a patient affected by chronic myeloid leukemia and treated with imatinib since 2002. A review of all the available literature regarding the imatinib‐related hyperpigmentation was performed, and one additional case was analyzed. Due to the possibility of a post‐inflammatory hyperpigmentation, all cases of pigmentary changes previously characterized by a rash and/or pruritus in the same body areas were excluded. Results Thirty cases of well‐documented imatinib‐related hyperpigmentation were described in literature. In our case, imatinib therapy was well tolerated for several years, and it led to an excellent hematological and cytogenetic response. However, the patient gradually developed a blue‐gray pigmentation that involved the nose, fingernails, toenails, pretibial regions, posterior axillary folds, and hard palate. Other causes of pigmentary changes were excluded, and histopathological examination confirmed the clinical suspicion of imatinib‐related hyperpigmentation. Conclusions Hyperpigmentation induced by imatinib is an adverse reaction rarely described in literature. The underlying pathogenetic mechanisms are not yet completely clear, and further studies are necessary to elucidate them. Currently, no treatment is required for this condition, and there is no indication to discontinue imatinib treatment.
机译:摘要背景伊替尼甲磺酸盐是一种酪氨酸激酶抑制剂,用作慢性髓性白血病患者的一线治疗,但也表明了其他血液学疾病和实体瘤。伊马替尼治疗通常与低分成有关,但在文献中只描述了少数过度沉降病例。方法报告,涉及受慢性骨髓白血病影响的患者的口腔粘膜,皮肤和钉子的第一种含有伊马替尼相关的高差异,并自2002年以来用伊马替尼治疗。关于伊马替尼相关的超差异的所有可用文献的审查是进行了,并分析了一个额外的案例。由于炎症后性质的可能性,以前的所有颜料变化的含量变化的含量变化,其特征在于同一体内区域的皮疹和/或瘙痒。结果文献中描述了30例文献纯净的伊替尼相关的高差异。在我们的情况下,伊马替尼治疗几年耐受良好,它导致了出色的血液学和细胞遗传学反应。然而,患者逐渐开发出一种涉及鼻子,指甲,脚趾甲,前腋褶和硬腭的蓝灰色色素沉着。排除了颜料变化的其他原因,组织病理学检查证实了伊马替尼相关的高差异的临床怀疑。结论伊马​​替尼诱导的高差异是文献中很少描述的不利反应。潜在的致病机制尚不清楚,并且需要进一步的研究来阐明它们。目前,这种情况不需要治疗,并且没有指示停止伊马替尼治疗。

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