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皮肤科光动力疗法。

Photodynamic therapy in dermatology.

机构信息

Department of Dermatology, University Clinic of Regensburg, Germany.

出版信息

J Dtsch Dermatol Ges. 2010 Jun;8(6):454-64. doi: 10.1111/j.1610-0387.2010.07343.x. Epub 2010 Feb 3.

DOI:10.1111/j.1610-0387.2010.07343.x
PMID:20136674
Abstract

Photodynamic therapy (PDT) is a modern therapy modality, based upon the application of a photosensitizing agent like aminolevulinic acid, a physiological precursor of porphyrins, onto the tissue followed by illumination with light of the visible wavelength spectrum. During this oxygen-dependent reaction, reactive oxygen species (ROS) are generated that have immunomodulatory or cytotoxic effects. PDT shows excellent cosmetic results especially for its key indication in dermatology - the treatment of non-melanoma skin cancer. The associated pain and the low tissue penetration are the most frequent limiting factors of PDT. We review basic principles and recent developments in photosensitizers and light sources. Key oncological and non-oncological indications are presented as well.

摘要

光动力疗法(PDT)是一种现代治疗方法,基于将光敏剂如氨基酮戊酸(ALA),卟啉的生理前体,应用于组织,然后用可见波长光谱的光照射。在这个依赖于氧气的反应中,会产生具有免疫调节或细胞毒性作用的活性氧(ROS)。PDT 显示出极好的美容效果,特别是在皮肤科的主要适应症 - 非黑色素瘤皮肤癌的治疗中。相关的疼痛和低组织穿透性是 PDT 最常见的限制因素。我们回顾了光敏剂和光源的基本原理和最新进展。还介绍了主要的肿瘤学和非肿瘤学适应症。

相似文献

1
Photodynamic therapy in dermatology.皮肤科光动力疗法。
J Dtsch Dermatol Ges. 2010 Jun;8(6):454-64. doi: 10.1111/j.1610-0387.2010.07343.x. Epub 2010 Feb 3.
2
Photodynamic therapy in dermatology--an update 2008.皮肤病学中的光动力疗法——2008年最新进展
J Dtsch Dermatol Ges. 2008 Oct;6(10):839-45, 839-46. doi: 10.1111/j.1610-0387.2008.06697.x. Epub 2008 Apr 9.
3
Photodynamic therapy: Dermatology and ophthalmology as main fields of current applications in clinic.光动力疗法:皮肤科和眼科作为目前临床应用的主要领域。
Biomed Mater Eng. 2008;18(4-5):319-27.
4
Photodynamic therapy in dermatology.皮肤科中的光动力疗法。
Eur J Dermatol. 2000 Oct-Nov;10(7):568-75; discussion 576.
5
The advantages of aminolevulinic acid photodynamic therapy in dermatology.氨基乙酰丙酸光动力疗法在皮肤科的优势。
J Dermatolog Treat. 2002;13 Suppl 1:S3-11. doi: 10.1080/095466302317414645.
6
Photodynamic therapy in dermatology.皮肤科中的光动力疗法。
Eur J Dermatol. 2006 Jul-Aug;16(4):340-8.
7
Photodynamic therapy in dermatology: history and horizons.皮肤科中的光动力疗法:历史与展望
J Drugs Dermatol. 2004 Jan-Feb;3(1 Suppl):S8-25.
8
[Photodynamic therapy: new indications].[光动力疗法:新适应症]
Actas Dermosifiliogr. 2007 Jul-Aug;98(6):377-95.
9
The use of photodynamic therapy in dermatology.光动力疗法在皮肤科的应用。
G Ital Dermatol Venereol. 2010 Oct;145(5):613-30.
10
Photodynamic therapy in dermatology: current treatments and implications.皮肤科中的光动力疗法:当前治疗方法及影响
Coll Antropol. 2012 Dec;36(4):1477-81.

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Treatment of nonmelanoma skin cancer with pro-differentiation agents and photodynamic therapy: Preclinical and clinical studies (Review).促分化剂和光动力疗法治疗非黑素瘤皮肤癌:临床前和临床研究(综述)。
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3
Management of keratinocyte carcinoma - Special considerations in the elderly.
角质形成细胞癌的管理——老年人的特殊考虑因素
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4
Regression Analysis of Protoporphyrin IX Measurements Obtained During Dermatological Photodynamic Therapy.皮肤科光动力治疗期间获得的原卟啉IX测量值的回归分析
Cancers (Basel). 2019 Jan 10;11(1):72. doi: 10.3390/cancers11010072.
5
Improving in vitro photodynamic therapy through the development of a novel iron chelating aminolaevulinic acid prodrug.通过开发新型铁螯合氨基酮戊酸前药来提高体外光动力疗法。
Photodiagnosis Photodyn Ther. 2019 Mar;25:157-165. doi: 10.1016/j.pdpdt.2018.12.005. Epub 2018 Dec 13.
6
An experimental investigation of a novel iron chelating protoporphyrin IX prodrug for the enhancement of photodynamic therapy.一种新型铁螯合原卟啉IX前药用于增强光动力疗法的实验研究。
Lasers Surg Med. 2018 Jul;50(5):552-565. doi: 10.1002/lsm.22809. Epub 2018 Mar 31.
7
Combined Treatments with Photodynamic Therapy for Non-Melanoma Skin Cancer.光动力疗法联合治疗非黑色素瘤皮肤癌
Int J Mol Sci. 2015 Oct 28;16(10):25912-33. doi: 10.3390/ijms161025912.
8
[New developments in laser therapy].[激光治疗的新进展]
Hautarzt. 2012 Apr;63 Suppl 1:59-66. doi: 10.1007/s00105-011-2297-4.
9
The application of Levulan-based photodynamic therapy with imiquimod in the treatment of recurrent basal cell carcinoma.艾拉光动力联合咪喹莫特治疗复发性基底细胞癌的应用。
Med Sci Monit. 2012 Feb;18(2):PI5-9. doi: 10.12659/msm.882449.