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本文引用的文献

1
Advanced management of venous malformation with ethanol sclerotherapy: mid-term results.乙醇硬化疗法对静脉畸形的高级管理:中期结果
J Vasc Surg. 2003 Mar;37(3):533-8. doi: 10.1067/mva.2003.91.
2
Advanced management of congenital vascular malformations: a multidisciplinary approach.先天性血管畸形的高级管理:多学科方法。
Cardiovasc Surg. 2002 Dec;10(6):523-33. doi: 10.1016/s0967-2109(02)00072-8.
3
[Pulmonary embolism in sclerotherapy for a venous malformation in a child under general anesthesia].
Ann Fr Anesth Reanim. 2001 Jun;20(6):556-8. doi: 10.1016/s0750-7658(01)00421-x.
4
New experiences with absolute ethanol sclerotherapy in the management of a complex form of congenital venous malformation.无水乙醇硬化疗法治疗复杂型先天性静脉畸形的新经验
J Vasc Surg. 2001 Apr;33(4):764-72. doi: 10.1067/mva.2001.112209.
5
[Treatment of low-pressure vascular malformations by injection of Ethibloc. Study of 19 cases and analysis of complications].[注射乙碘油治疗低压性血管畸形。19例研究及并发症分析]
Rev Stomatol Chir Maxillofac. 2000 Oct;101(4):181-8.
6
Percutaneous sclerotherapy for venous malformation of the lips: a retrospective study of 23 patients.经皮硬化治疗唇部静脉畸形:23例患者的回顾性研究
Neuroradiology. 2000 Sep;42(9):692-6. doi: 10.1007/s002340000364.
7
[The use of an alcohol gel of ethyl cellulose in the treatment of venous malformations].
Rev Stomatol Chir Maxillofac. 2000 Jan;101(1):30-2.
8
Sclerotherapy of craniofacial venous malformations: complications and results.颅面部静脉畸形的硬化治疗:并发症与结果
Plast Reconstr Surg. 1999 Jul;104(1):1-11; discussion 12-5.
9
[Superficial vascular malformations: classification and histopathology].
Ann Pathol. 1999 Jun;19(3):253-64.
10
[Hemangioma and superficial arteriovenous malformations].[血管瘤与浅表动静脉畸形]
Arch Mal Coeur Vaiss. 1999 May;92(5):649-58.

一种治疗静脉畸形的新型硬化剂。23例病例研究。

A new sclerosing agent in the treatment of venous malformations. Study on 23 cases.

作者信息

Sannier K, Dompmartin A, Théron J, Labbé D, Barrellier M T, Leroyer R, Touré P, Leroy D

机构信息

Services de Dermatologie, Centre Hospitalier Universitaire de Caen, Cedex; France -

出版信息

Interv Neuroradiol. 2004 Jun 29;10(2):113-27. doi: 10.1177/159101990401000203. Epub 2004 Oct 22.

DOI:10.1177/159101990401000203
PMID:20587223
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3464441/
Abstract

Absolute ethanol is the most effective agent in the treatment of venous malformation (VM) although it is quite risky to use because of the danger of diffusion beyond the target. To reduce this risk, we have developed an alcoholic sclerosing solution that is less diffusible. The viscosity of absolute ethanol was enhanced with monographic ethyl-cellulose at a concentration of 5.88% ie 0.75 g in 15 ml of absolute ethanol 95%. 23 patients with VM located on the buttock (1), hand (2), leg (1) and face (19) were treated. A mean volume of 1.99 ml of the solution was injected directly into the VM. Each patient had an average of 2.8 procedures. Sixteen patients were done under general anaesthesia and seven with local anaesthesia. Evaluation was performed by the patient, the dermatologist of the treating multidisciplinary team and a dermatological group not involved in the treatment of the patients. Patients were evaluated after a mean delay of 24.52 months. Evaluation of the cosmetic result was made with a five point scale and the global result with a three point scale. VM pain was evaluated by the patients with a Visual Analogue Scale. The aesthetic results were graded as satisfactory (> 3) for the patient and the dermatologist of the multidisciplinary team. However the results were not as good with the independent dermatological group evaluation. The pain was significantly less important after the treatment (p << 0.001). Among the 23 patients, the local adverse events were nine necrosis with or without ethylcellulose fistula followed by only two surgical procedures. There were no systemic adverse events. Sclerotherapy of VM is usually performed with absolute ethanol or ethibloc. The main advantage of our sclerosing mixture is that it expands like a balloon when injected slowly in a aqueous media. Because of the important increase in viscosity the volume of injected solution is much lower than ethanol alone and the risk of systemic reactions is lower. Contrary to ethibloc, post-sclerosing surgery is not necessary because sub-cutaneous ethylcellulose disappears secondarily.

摘要

无水乙醇是治疗静脉畸形(VM)最有效的药物,尽管由于其有扩散至靶区以外的风险,使用起来颇具危险性。为降低此风险,我们研发了一种扩散性较小的酒精硬化溶液。通过在无水乙醇中加入浓度为5.88%(即95%的15毫升无水乙醇中加入0.75克)的乙基纤维素来提高无水乙醇的黏度。对23例VM患者进行了治疗,这些患者的VM分别位于臀部(1例)、手部(2例)、腿部(1例)和面部(19例)。平均向VM内直接注射1.99毫升该溶液。每位患者平均接受2.8次治疗。16例患者在全身麻醉下进行治疗,7例采用局部麻醉。由患者、参与治疗的多学科团队中的皮肤科医生以及未参与这些患者治疗的皮肤科小组进行评估。患者在平均24.52个月的延迟后接受评估。使用五点量表对美容效果进行评估,使用三点量表对总体效果进行评估。患者通过视觉模拟量表评估VM疼痛情况。对于患者和多学科团队中的皮肤科医生而言,美容效果被评为满意(>3分)。然而,独立皮肤科小组的评估结果则没那么理想。治疗后疼痛明显减轻(p << 0.001)。在这23例患者中,局部不良事件为9例坏死,伴或不伴有乙基纤维素瘘管形成,随后仅进行了2次外科手术。未发生全身不良事件。VM硬化治疗通常使用无水乙醇或乙碘油。我们的硬化混合物的主要优点是,当缓慢注射到水性介质中时,它会像气球一样膨胀。由于黏度显著增加,注射溶液的体积比单独使用乙醇时要低得多,全身反应的风险也更低。与乙碘油不同,硬化治疗后无需进行手术,因为皮下乙基纤维素会继发消失。