Oral Medicine
Sclerotherapy of benign oral vascular lesion with ethanolamine oleate: An open clinical trial with 30 lesions

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Objective

The objective of this study was to report and discuss the results from treatment of benign oral vascular lesions with ethanolamine oleate.

Study design

Twenty-seven patients with 30 examples of oral vascular malformation, hemangioma, or varix were treated with intralesional injections of 1.25% or 2.5% ethanolamine oleate at an interval of 15 days between each application. The lesions were divided into 2 categories: (1) lesions of 20 mm or less and (2) those greater than 20 mm. Subsequently, the Mann-Whitney test was used a means of statistical analysis.

Results

Although the number of injections varied from patient to patient, all lesions responded to the treatment, showing total clinical regression. Lesions of 20 mm or less needed a lesser number of applications than those greater than 20 mm (P < .05).

Conclusions

Ethanolamine oleate is a 100% effective sclerosant agent for treatment of benign oral vascular lesions. In this study, no difference was found between the 2 concentrations applied.

Section snippets

Study design

An open clinical trial of 27 patients with 30 examples of oral vascular malformation, hemangioma, or varix were treated with intralesional injections of 1 mL of 1.25% or 2.5% EO. A 15-day interval between each application was applied, until the total clinical resolution of the lesion had occurred. The lesions were then divided into 2 groups: (1) lesions of 20 mm or less, and (2) those of greater than 20 mm. Here, the Mann-Whitney test was used as a means of the statistical analysis.

Results

All 30 lesions responded to the treatment with total clinical resolution. None of the patients showed signs of scarring. After the application of EO, 17 patients complained of pain, swelling, redness, and/or burning regardless of the concentrations. These symptoms were present only up to 72 hours after applications. No information about the symptoms was obtained from the other patients.

The number of applications required for the treatment of all lesions varied from 1 to 10 (mean average of

Discussion

In the present study, the use of 1.25% or 2.5% EO as a choice treatment of benign oral vascular lesions was considered 100% satisfactory. Our patients reported symptoms of pain, swelling, redness, and/or burning after the application of EO, but for only 72 hours. Choi et al14 also reported similar symptoms. This research, therefore, represents the first large series of cases of benign oral vascular lesions treated with EO. Therefore, 2 concentrations of EO (2.5% or 1.25%) were applied,

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    The authors thank National Council for Scientific and Technological Development (CNPq) and Foundation for Support of Research in Minas Gerais (FAPEMIG) for assistance. Mesquita, Aguiar, and Gomez are research fellows of the CNPq.

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