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Civatte皮肤异色病
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作者 杨敏 鲍迎秋 +1 位作者 高小曼 常建民 《临床皮肤科杂志》 CAS CSCD 北大核心 2011年第4期191-192,共2页
患者女,37岁,戏剧演员。 主诉:面颈部褐色色素沉着斑21年,加重2年。 现病史:患者自16岁化彩妆后双颊部开始出现淡褐色斑,无自觉症状。近2年皮损逐渐蔓延至颧部、额部及颈部,并融合呈网状,颜色渐深。同时下腹部、腹股沟也有类... 患者女,37岁,戏剧演员。 主诉:面颈部褐色色素沉着斑21年,加重2年。 现病史:患者自16岁化彩妆后双颊部开始出现淡褐色斑,无自觉症状。近2年皮损逐渐蔓延至颧部、额部及颈部,并融合呈网状,颜色渐深。同时下腹部、腹股沟也有类似皮损,但未呈网状,于2009年11月来我科就诊。患者近10年未再接触彩妆。 展开更多
关键词 皮肤异色病 civatte
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Civatte皮肤异色病1例
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作者 赵庆利 史飞 +1 位作者 原晓斌 王毅侠 《临床皮肤科杂志》 CAS CSCD 北大核心 2005年第4期250-251,共2页
关键词 皮肤异色病 civatte
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Civatte皮肤异色病1例
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作者 张景龙 赵庆利 王毅侠 《中国皮肤性病学杂志》 CAS 北大核心 2008年第1期44-45,共2页
患者女,50岁。面部皮肤褐色斑片40余年。查体见面颈部弥漫分布黑褐色斑片,两颊呈网状分布,伴有白色斑点、毛细血管扩张和轻度萎缩。皮肤组织病理示:表皮变薄,基底细胞液化变性,真皮浅层血管周围炎细胞浸润,见明显噬色素细胞。诊断:Civa... 患者女,50岁。面部皮肤褐色斑片40余年。查体见面颈部弥漫分布黑褐色斑片,两颊呈网状分布,伴有白色斑点、毛细血管扩张和轻度萎缩。皮肤组织病理示:表皮变薄,基底细胞液化变性,真皮浅层血管周围炎细胞浸润,见明显噬色素细胞。诊断:Civatte皮肤异色病。 展开更多
关键词 色素性皮肤病 civatte皮肤异色病
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Civatte皮肤异色病1例
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作者 周蓉颖 文翔 +1 位作者 李咏 李利 《临床皮肤科杂志》 CAS CSCD 北大核心 2016年第2期106-106,共1页
患者女,54岁。因颈部网状褐色斑7年余,加重2年余,于2014年8月5日来我院门诊就诊。7年余前患者颈部出现网状淡褐色斑,无明显自觉症状,自诉季节变化褐色斑无明显加重.未予任何诊治。2年余前色素斑颜色逐渐加深,遂到我院就诊。患者... 患者女,54岁。因颈部网状褐色斑7年余,加重2年余,于2014年8月5日来我院门诊就诊。7年余前患者颈部出现网状淡褐色斑,无明显自觉症状,自诉季节变化褐色斑无明显加重.未予任何诊治。2年余前色素斑颜色逐渐加深,遂到我院就诊。患者系农民,家住四川甘孜州,地处光照强烈地区。 展开更多
关键词 civatte皮肤异色病
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Civatte皮肤异色病的临床和流行病学研究
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作者 Katoulis A.C Stavrianeas N.G +1 位作者 Georgala S 刘芯 《世界核心医学期刊文摘(皮肤病学分册)》 2006年第1期16-17,共2页
Background: Although a common dermatosis, idiopathic poikiloderma of the face and neck has not been studied in depth for decades. Objectives: To reassess the clinical and epidemiological characteristics of poikiloderm... Background: Although a common dermatosis, idiopathic poikiloderma of the face and neck has not been studied in depth for decades. Objectives: To reassess the clinical and epidemiological characteristics of poikiloderma of Civatte (PC). Ma terial and methods: Fifty consecutive patients with PC. Evaluation included hist ory taking and physical examination. Epidemiological and clinical parameters wer e recorded and analysed. The literature from 1923 until today, was reviewed thor oughly. Results: The frequency of PC among dermatologic patients was estimated t o be 1.4%. There were 34 females (68%) and 16 males in the present study. The mean age at diagnosis was 47.8 years for females and 61.7 years for males. The m ajority (88%) had skin phototype II or III. Among females, 26 were at their per imenopausal stage, including three cases of iatrogenic menopause. Four patients reported that other blood-related family members also had PC. The v and the sid es of the neck and the upper chest were most often affected in a symmetric distr ibution. The face (preauricular and parotid region) was involved in 19 patients (38%). The erythematotelangiectatic clinical type predominated (58%), followed by the mixed (22%) and the pigmented type (20%). Almost half of the patients (46%) were symptomatic (itching, burning and ’flushing’). The mean duration fro m onset to diagnosis was 6.2 years according to the patients’report. The course was usually slowly progressive (82%) and irreversible. Conclusions: PC shows c haracteristic features, supporting the theory that it represents a distinct enti ty. It is rather common in Greece. Although menopausalwomen predominated in our cohort, men were not uncommonly affected and were diagnosed at an older age. Bas ed on the predominating clinical feature, PC can be classified into three clinic al forms. Symmetry and sparing of the anatomically shaded areas of the neck are highly characteristic for PC. Face involvement was not as common and as severe a s it had been considered in the past. Recognition of clinical type is important for the selection of the most appropriate treatment, which, despite the advent o f novel modalities, remains problematic. 展开更多
关键词 皮肤异色病 civatte 流行病学研究 分析流行病学 毛细血管扩张 面颈部 临床参数 体格检查
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血管萎缩性皮肤异色病1例 被引量:1
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作者 房慧媚 王红梅 +3 位作者 陈丹 赵爽 顾安康 纪华安 《中国中西医结合皮肤性病学杂志》 CAS 2016年第4期242-243,共2页
患者男,80岁。全身棕褐色斑、间有白色斑点,伴瘙痒8年。专科检查:颜面、颈部、躯干及四肢可见红斑、棕褐色网状色素沉着、色素减退斑,间有毛细血管扩张,皮损部位萎缩变薄。皮肤组织病理检查:表皮轻度角化过度,棘层萎缩,基底细胞液化,真... 患者男,80岁。全身棕褐色斑、间有白色斑点,伴瘙痒8年。专科检查:颜面、颈部、躯干及四肢可见红斑、棕褐色网状色素沉着、色素减退斑,间有毛细血管扩张,皮损部位萎缩变薄。皮肤组织病理检查:表皮轻度角化过度,棘层萎缩,基底细胞液化,真皮浅层水肿,血管周围较多淋巴细胞、噬色素细胞浸润。结合临床诊断:血管萎缩性皮肤异色病。 展开更多
关键词 血管萎缩性皮肤异色病 civatte皮肤异色病 先天性角化不良
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