• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

亚甲蓝染色在马拉色菌检测中的应用

[Application of methylene blue staining in detection of Malassezia].

作者信息

Xiong Lin, Dai Ya-ling

机构信息

Department of Dermato-venereology, West China Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2004 Mar;35(2):277-9.

PMID:15071940
Abstract

OBJECTIVE

To assess the value of methylene blue and parker ink staining in the detection of Malassezia.

METHODS

Detecting Malassezia in three dermatoses samples (pityriasis versicolor, Malassezia folliculitis and dandruff) stained by methylene blue (3 g/L) or parker ink. Comparing the effectiveness and the positive rates of Malassezia detection between the two staining methods. Staining Malassezia and Candida and comparing the specificity of the two staining methods in staining Malassezia.

RESULTS

Dark blue hyphae and spores were observed in smears stained by methylene blue, and light blue hyphae and spores were observed in smears stained by parker ink. Hyphae and spores were easy to identify on the background. The positive rates of methylene blue and parker ink for detecting Malassezia in the three dermatoses were 96% and 94% respectively. There was no significant difference between the two dye liquors in the positive rate for deterting Malassezia. Both Malassezia and Candida could be stained by methylene blue; nevertheless, only Malassezia could be stained by parker ink.

CONCLUSION

Both methylene blue and parker ink staining can be used to detect Malassezia, but parker ink has higher specificity in Malassezia staining.

摘要

目的

评估亚甲蓝和派克墨水染色法在检测马拉色菌中的价值。

方法

用亚甲蓝(3 g/L)或派克墨水对三种皮肤病样本(花斑癣、马拉色菌毛囊炎和头皮屑)进行染色以检测马拉色菌。比较两种染色方法检测马拉色菌的有效性和阳性率。对马拉色菌和念珠菌进行染色,比较两种染色方法对马拉色菌染色的特异性。

结果

亚甲蓝染色涂片可见深蓝色菌丝和孢子,派克墨水染色涂片可见浅蓝色菌丝和孢子。菌丝和孢子在背景上易于识别。亚甲蓝和派克墨水检测三种皮肤病中马拉色菌的阳性率分别为96%和94%。两种染液检测马拉色菌的阳性率无显著差异。亚甲蓝可对马拉色菌和念珠菌进行染色;然而派克墨水仅可对马拉色菌进行染色。

结论

亚甲蓝和派克墨水染色均可用于检测马拉色菌,但派克墨水对马拉色菌染色具有更高的特异性。

相似文献

1
[Application of methylene blue staining in detection of Malassezia].亚甲蓝染色在马拉色菌检测中的应用
Sichuan Da Xue Xue Bao Yi Xue Ban. 2004 Mar;35(2):277-9.
2
New contrast stain for the rapid diagnosis of pityriasis versicolor.用于花斑糠疹快速诊断的新型对比染色剂。
Arch Dermatol. 2008 Aug;144(8):1058-9. doi: 10.1001/archderm.144.8.1058.
3
Skin diseases associated with Malassezia species in humans. Clinical features and diagnostic criteria.与人类马拉色菌属相关的皮肤疾病。临床特征及诊断标准。
Parassitologia. 2008 Jun;50(1-2):69-71.
4
Malassezia Baillon, emerging clinical yeasts.马拉色菌属,新兴的临床酵母菌种。
FEMS Yeast Res. 2005 Dec;5(12):1101-13. doi: 10.1016/j.femsyr.2005.05.006. Epub 2005 Jul 12.
5
Distribution of Malassezia species in pityriasis versicolor and seborrhoeic dermatitis in Greece. Typing of the major pityriasis versicolor isolate M. globosa.希腊花斑糠疹和脂溢性皮炎中马拉色菌属的分布。花斑糠疹主要分离株球形马拉色菌的分型。
Br J Dermatol. 2006 May;154(5):854-9. doi: 10.1111/j.1365-2133.2005.07114.x.
6
Coexistence of pityriasis versicolor and erythrasma.花斑糠疹与红癣共存。
Mycoses. 2004 Aug;47(7):343-5. doi: 10.1111/j.1439-0507.2004.00997.x.
7
Epidemiological characteristics of Malassezia folliculitis and use of the May-Grünwald-Giemsa stain to diagnose the infection.马拉色菌性毛囊炎的流行病学特征及应用瑞氏-吉姆萨染色诊断感染。
Diagn Microbiol Infect Dis. 2013 Aug;76(4):450-7. doi: 10.1016/j.diagmicrobio.2013.04.011. Epub 2013 May 22.
8
Epidemiology of pityriasis versicolor in Adana, Turkey.土耳其阿达纳花斑糠疹的流行病学
J Dermatol. 2009 Jul;36(7):377-82. doi: 10.1111/j.1346-8138.2009.00663.x.
9
Uncommon cases of pityriasis versicolor.花斑糠疹的罕见病例。
Parassitologia. 2008 Jun;50(1-2):93-4.
10
Skin diseases associated with Malassezia species.与马拉色菌属相关的皮肤疾病。
J Am Acad Dermatol. 2004 Nov;51(5):785-98. doi: 10.1016/j.jaad.2003.12.034.