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Hyperpigmentation in Laugier-Hunziker syndrome.

机译:Laugier-Hunziker综合征中的色素沉着过度。

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A 60-year-old nonsmoking Chinese woman presented with a 40-year history of progressive blackish pigmentation of her tongue, oral mucosa and lips (Figure 1A; Appendix 1, available at www.cmaj.ca/lookup /suppl/doi:10.1503/cmaj.H0211/-/DCl). In addition, she had a 10-year history of longitudinal pigmented bands on parts of her fingernails (Figure IB). There was no relevant drug history, and no other family members were affected. Histology of the lesions of the lower lip showed a substantial increase of melanin in the basal keratinocytes but no increase in the number of melanocytes. Serum cortisol and adrenocorti-cotropic hormone levels were within normal limits. The patient underwent an upper gastrointestinal study, barium enema and colonoscopy, which showed no evidence of polyps. A diagnosis of Laugier-Hunziker syndrome was made. In follow-up over the next five years, an increasing number of pigmented macules was noted.
机译:一名60岁不吸烟的中国妇女,其舌头,口腔粘膜和嘴唇渐渐发黑,已有40年历史(图1A;附录1,网址为www.cmaj.ca/lookup/suppl/doi:10.1503) /cmaj.H0211/-/DCl)。另外,她在指甲的部分上有10年的纵向色素带历史(图1B)。没有相关的毒品史,也没有其他家庭成员受到影响。下唇病变的组织学显示,基底角质形成细胞中的黑色素显着增加,但黑色素细胞的数量没有增加。血清皮质醇和肾上腺皮质激素水平在正常范围内。该患者进行了上消化道检查,钡灌肠和结肠镜检查,未发现息肉迹象。诊断为Laugier-Hunziker综合征。在接下来的五年的随访中,发现了越来越多的色素斑。

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