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Sclerotherapy as an esthetic indication in oral vascular malformations: a case series How to cite this article: Manzano BR, Premoli AM, Santaella NG, Ikuta CR, Rubira CM, da Silva Santos PS. Sclerotherapy as an esthetic indication in oral vascular malformations: a case series. An Bras Dermatol. 2019;94:521-6. ☆☆ ☆☆ Study conducted at the Graduate Studies Clinic in Stomatology and Radiology, Faculdade de Odontologia de Bauru, Universidade de São Paulo, Bauru, SP, Brazil.

Abstract

Background

The use of monoethanolamine oleate 5% is effective for the treatment of vascular malformations with low blood flow.

Objectives

To report a case series of vascular malformations in the mouth and oral cavity treated with monoethanolamine oleate 5%.

Methods

A retrospective descriptive study was performed in electronic patient charts covering seven years. Patient demographics, diagnostic resources, lesion site, size, and number of applications of monoethanolamine oleate 5% were collected.

Results

A total of 21 vascular malformations were recorded, located mostly on the lower lip (52.3%) and resolved in a single application in 14 patients. The authors found 19 patients treated with sclerotherapy. Thirteen were women and six were men, with a mean age of 61 years.

Study limitation

Small sample size.

Conclusions

Sclerotherapy is an effective treatment for vascular malformations of the lips and oral cavity, with resolution after only one or two applications (n = 16).

KEYWORDS
Mouth; Sclerotherapy; Vascular malformations

Introduction

Vascular malformations (VMs) are lesions of the vascular or lymphatic system that can affect any part of the body, but which are common on the head and neck region.11 Johann AC, Aguiar MC, do Carmo MA, Gomez RS, Castro WH, Mesquita RA. Sclerotherapy of benign oral vascular lesion with ethanolamine oleate: an open clinical trial with 30 lesions. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;100:579-84. Due to discrepancies in the literature as to the correct nomenclature, in 1996 the International Society for the Study of Vascular Anomalies (ISSVA) classified vascular anomalies as vascular tumors (hemangiomas) and vascular malformations, based on the lesions’ biological and pathological characteristics.22 Wójcicki P, Wójcicka K. Epidemiology, diagnostics and treatment of vascular tumours and malformations. Adv Clin Exp Med. 2014;23:475-84.,33 Clemens RK, Pfammatter T, Meier TO, Alomari AI, Amann-Vesti BR. Vascular malformations revisited. Vasa. 2015;44:5-22.

Vascular tumors develop through the vessels’ cell growth and proliferation. Meanwhile, VMs are characterized as a defect in the vessels’ maturation and vascular morphogenesis, caused mainly by a dysfunction in the regulation of the pathways in embryogenesis and vasculogenesis.33 Clemens RK, Pfammatter T, Meier TO, Alomari AI, Amann-Vesti BR. Vascular malformations revisited. Vasa. 2015;44:5-22. VMs can be divided into low-flow and high-flow: low-flow VMs consist of a venous, capillary, or lymphatic component, while high-flow VMs consist of an arterial or arteriovenous component.44 Enjolras O, Wassef M, Chapot R. Color atlas of vascular tumors and vascular malformations. New York: Cambridge University Press; 2007.

VMs usually occur in children and young adults. In the oral cavity, they are normally observed on the lips, tongue, buccal mucosa, and palate.55 Johnson PL, Eckard DA, Brecheisen MA, Girod DA, Tsue TT. Percutaneous ethanol sclerotherapy of venous malformations of the tongue. AJNR Am J Neuroradiol. 2002;23:779-82.

6 Buckmiller LM. Update on hemangiomas and vascular malformations. Curr Opin Otolaryngol Head Neck Surg. 2004;12:476-87.
-77 Hoque S, Das BK. Treatment of venous malformations with ethanolamine oleate: a descriptive study of 83 cases. Pediatr Surg Int. 2011;27:527-31. VMs do not regress spontaneously and can expand, and can be either single or multiple.77 Hoque S, Das BK. Treatment of venous malformations with ethanolamine oleate: a descriptive study of 83 cases. Pediatr Surg Int. 2011;27:527-31. The clinical manifestations consist of pain, ulcerations, bleeding, functional limitations, and esthetic alterations.55 Johnson PL, Eckard DA, Brecheisen MA, Girod DA, Tsue TT. Percutaneous ethanol sclerotherapy of venous malformations of the tongue. AJNR Am J Neuroradiol. 2002;23:779-82.,88 Dubois J, Soulez G, Oliva VL, Berthiaume MJ, Lapierre C, Therasse E. Soft-tissue venous malformations in adult patients: imaging and therapeutic issues. Radiographics. 2001;21:1519-31.,99 García ED, Jiménez IF, Carrera MT, González FS. Hemangiomas y malformaciones vasculares. ¿Qué se puede hacer?. Bol Pediatr. 2001;41:137-43. The etiology may involve trauma or pregnancy and other hormonal factors that can induce the lesions’ growth.33 Clemens RK, Pfammatter T, Meier TO, Alomari AI, Amann-Vesti BR. Vascular malformations revisited. Vasa. 2015;44:5-22.

Treatment indication in VMs depends on a diagnosis that specifies the vascular type (arterial, venous, and/or lymphatic) and type of blood flow. The treatment options are: laser therapy, surgical excision, embolization, electrosurgery, and sclerotherapy combined with surgery.77 Hoque S, Das BK. Treatment of venous malformations with ethanolamine oleate: a descriptive study of 83 cases. Pediatr Surg Int. 2011;27:527-31.,1010 Zheng JW, Mai HM, Zhang L, Wang YA, Fan XD, Su LX, et al. Guidelines for the treatment of head and neck venous malformations. Int J Clin Exp Med. 2013;6:377-89.,1111 Ogawa Y, Inoue K. Electrothrombosis as a treatment of cirsoid angioma in the face and scalp and varicosis of the leg. Plast Reconstr Surg. 1982;70:310-8.

Sclerotherapy is a conservative technique that consists of intralesional injection of sclerosing agents, causing inflammation in the vessels followed by occlusion and vascular sclerosis, resulting in regression of the lesion.1212 Horbach SE, Lokhorst MM, Saeed P, de Goüyon Matignon de Pontouraude CM, Rothová A, van der Horst CM. Sclerotherapy for low-flow vascular malformations of the head and neck: a systematic review of sclerosing agents. J Plast Reconstr Aesthet Surg. 2016;69:295-304. The sclerosing agents used to treat VMs include monoethanolamine oleate 5%, reported in the literature as a safe and efficient method with low toxicity for the treatment of these lesions in various regions of the body.11 Johann AC, Aguiar MC, do Carmo MA, Gomez RS, Castro WH, Mesquita RA. Sclerotherapy of benign oral vascular lesion with ethanolamine oleate: an open clinical trial with 30 lesions. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;100:579-84.,1313 Ribeiro MC, de Mattos Camargo Grossmann S, do Amaral MBF, de Castro WH, Navarro TP, et al. Effectiveness and safety of foam sclerotherapy with 5% ethanolamine oleate in the treatment of low-flow venous malformations in the head and neck region: a case series. Int J Oral Maxillofac Surg. 2018;47:900-7.,1414 Hyodoh H, Hori M, Akiba H, Tamakawa M, Hyodoh K, Hareyama M. Peripheral vascular malformations: imaging, treatment approaches, and therapeutic issues. Radiographics. 2005;25(Suppl. 1):S159-71.

The study aims to report 19 clinical cases of oral VMs that were treated with sclerotherapy using the application of monoethanolamine oleate 5% as monotherapy in VMs of the mouth, describing the diagnostic approach and therapeutic indication.

Methods

Characterization and data collection

This is a retrospective descriptive study based on collection of data from patients with oral VMs submitted to sclerotherapy with monoethanolamine oleate 5%. A search was conducted in the electronic patient file system, using the terms “vascular,” “vascular malformations,” and “vascular lesions,” from 2011 to 2017, resulting in 19 cases that were included in the current report. Demographic data were then collected, such as age, sex, and race of patients submitted to sclerotherapy. Data on the diagnostic resources used, location and size of the VMs, and number of applications of monoethanolamine oleate were also collected.

Diagnostic criteria and sclerotherapy

Diagnosis of VM began with the clinical observation of painless purplish vesicles or bullae with a soft consistency on palpation. There were frequent reports of a pulsatile sensation and increased volume during or after physical exercise. History of the lesions featured reports of trauma, puberty, pregnancy, or hormonal alterations prior to the lesion. In all the cases, diascopy showed changes in coloring, intralesional ischemia, and decrease or alteration in the shape, corroborating the presumptive diagnosis of VM.

When the VM was 5 mm in diameter or smaller and well demarcated on visual inspection and palpation, the treatment of choice was sclerotherapy, without complementary diagnostic imaging tests. However, for lesions greater than 5 mm with imprecise limits on visual inspection and palpation or with multiple lesions in the same elective region for sclerotherapy, and in which the history of the current disease was inconsistent with VM and/or with clinical aspects suggestive of tumors, Doppler ultrasound was performed, which provided an adequate diagnosis according to type of vascular content and blood flow velocity.44 Enjolras O, Wassef M, Chapot R. Color atlas of vascular tumors and vascular malformations. New York: Cambridge University Press; 2007. For cases in which the content was predominantly venous and low-flow, sclerotherapy remained indicated.

Application of the sclerosing solution followed the manufacturer's instructions. The sclerosing oil was diluted in anesthetic liquid at a proportion of 7:3 mL of monoethanolamine oleate 5% (0.7 mL) to mepivacaine 2% with epinephrine 1:100,000 (0.3 mL) in a 1 mL syringe. The first injection was applied in the central region of the VM, with introduction of the needle to a depth that included half the volume of the VM. Before injection of the sclerosing solution, positive aspiration of the blood vessel was verified to ensure correct intravascular application.

Ischemia and progressive increase in the pressure needed for the injection caused by the accumulation of the intralesional sclerosing solution were used as the criteria for interrupting application of the solution in that region. The needle/syringe was then redirected to another region of the VM where a new positive aspiration was observed before performing another injection. Per session, a maximum of 1 mL of sclerosing solution was applied, properly diluted, and for each application in a single region of the VM, the amount varied from 0.2 to 0.4 mL. Thus, per session, the sclerosing solution was injected in up to four different regions of a VM.

Results

The electronic patient chart search identified 19 patients that had undergone sclerotherapy in oral VMs, totaling 21 VMs, since two patients had two lesions. Mean age was 61 years, 13 patients (68%) were females, and 15 (79%) were white (Table 1). Lesions greater than 5 mm in diameter were found in six patients, and in these cases Doppler ultrasound was performed. In all the cases in this study, the VMs were of the venous type, with low blood flow. The most frequently affected region was the lower lip (52.3%), followed by the upper lip (23.8%), buccal mucosa (9.7%), labial mucosa (4.7%), both lips (4.7%), and labial commissure (4.7%) (Fig. 1).

Table 1
Distribution of patients treated with monoethanolamine oleate according to epidemiology and clinical characteristics of the lesions.

Figure 1
Distribution of location of the 21 oral vascular malformations.

The number of sessions varied according to the decrease in coloring and volume of the VMs, and especially with each individual patient's esthetic satisfaction. The patients returned for follow-up assessment, and when necessary a new session with application of the sclerosing solution was performed 20 days after the last injection. One to five sessions were performed in each lesion until obtaining a satisfactory result, and most required one (38.1%) or two (38.1%) applications of sclerosing solution. In three lesions (14.3%), three applications were performed; one lesion (4.75%) required four applications; and only one case (4.75%) required five applications (Table 1).

During the procedure, all the patients complained of a local burning sensation, and edema and mild ischemia were observed in the region. In the first post-procedure consultation, all the patients reported a sensation of hardening in the lesion's area, but only during the first 72 h after the procedure; only one patient reported tingling, and one patient also noted paresthesia in the region, but there were no complaints in the subsequent follow-up visits. In all the cases, there was a reduction in the volume and fading of the VMs, with a report of esthetic improvement in the treated area (Fig. 2).

Figure 2
(A) Initial clinical appearance of vascular malformation, purplish vesicle measuring 3 mm on lower lip (patient 16); (B) positive diascopy for vascular lesion performed during clinical examination; (C) application of monoethanolamine oleate 5% with positive aspiration of blood in the vascular lumen; (D) clinical appearance of lesion on seventh day post-procedure; (E) final clinical appearance of vascular lesion on 28th day post-procedure; (F) final negative diascopy of the region where the VM was previously located.

Discussion

In the current study, the VMs were found in adults and elderly, differing from the findings in the literature showing that they were more frequent in young people and young adults.1515 Choi YH, Han MH, O-Ki K, Cha SH, Chang KH. Craniofacial cavernous venous malformations: percutaneous sclerotherapy with use of ethanolamine oleate. J Vasc Interv Radiol. 2002;13:475-82.

16 Costa JR, Torriani MA, Hosni ES, D’Avila OP, de Figueiredo PJ. Sclerotherapy for vascular malformations in the oral and maxillofacial region: treatment and follow-up of 66 lesions. J Oral Maxillofac Surg. 2011;69:e88-92.
-1717 Balasundaram I, Al-Hadad I, Rehman K, McCafferty I, Monaghan A. The use of foam sclerotherapy to treat low-flow vascular malformations of the head and neck. J Surg Case Rep. 2014:2014, pii:rju095. They were more prevalent in women, corroborating other reports.77 Hoque S, Das BK. Treatment of venous malformations with ethanolamine oleate: a descriptive study of 83 cases. Pediatr Surg Int. 2011;27:527-31.,1717 Balasundaram I, Al-Hadad I, Rehman K, McCafferty I, Monaghan A. The use of foam sclerotherapy to treat low-flow vascular malformations of the head and neck. J Surg Case Rep. 2014:2014, pii:rju095. As for location, the VMs were found more frequently on the lips, also in agreement with the case series in the reviewed literature.55 Johnson PL, Eckard DA, Brecheisen MA, Girod DA, Tsue TT. Percutaneous ethanol sclerotherapy of venous malformations of the tongue. AJNR Am J Neuroradiol. 2002;23:779-82.,66 Buckmiller LM. Update on hemangiomas and vascular malformations. Curr Opin Otolaryngol Head Neck Surg. 2004;12:476-87.,1616 Costa JR, Torriani MA, Hosni ES, D’Avila OP, de Figueiredo PJ. Sclerotherapy for vascular malformations in the oral and maxillofacial region: treatment and follow-up of 66 lesions. J Oral Maxillofac Surg. 2011;69:e88-92.

VMs can be classified according to blood flow velocity, which can be slow (venous, lymphatic, and capillary VMs) or rapid (arterial and arteriovenous VMs).22 Wójcicki P, Wójcicka K. Epidemiology, diagnostics and treatment of vascular tumours and malformations. Adv Clin Exp Med. 2014;23:475-84.,1818 Buckmiller LM, Richter GT, Suen JY. Diagnosis and management of hemangiomas and vascular malformations of the head and neck. Oral Dis. 2010;16:405-18. Venous VMs appear on Doppler ultrasound as hypoechoic tubular structures, demonstrating a slow blood flow pattern.1919 Lidsky ME, Markovic JN, Miller MJ, Shortell CK. Analysis of the treatment of congenital vascular malformations using a multidisciplinary approach. J Vasc Surg. 2012;56:1355-62. Correct diagnosis is essential for the success of sclerotherapy, since efficient treatment requires prolonged contact between the sclerosing agent and the vascular wall; thus, sclerotherapy is most effective and safer in low-flow venous VMs.1515 Choi YH, Han MH, O-Ki K, Cha SH, Chang KH. Craniofacial cavernous venous malformations: percutaneous sclerotherapy with use of ethanolamine oleate. J Vasc Interv Radiol. 2002;13:475-82.

In this case series, VMs were diagnosed through a detailed clinical examination, with the semiotic procedure of diascopy, and by Doppler ultrasound in lesions greater than 5 mm. Thus, in all the cases the VMs were venous with slow blood flow, indicating sclerotherapy. In cases where the VM presented large caliber arteriovenous content with high blood flow, sclerotherapy was contraindicated.

Sclerotherapy is the treatment of choice for VMs, with a success rate of 70%-100%.11 Johann AC, Aguiar MC, do Carmo MA, Gomez RS, Castro WH, Mesquita RA. Sclerotherapy of benign oral vascular lesion with ethanolamine oleate: an open clinical trial with 30 lesions. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;100:579-84.,1616 Costa JR, Torriani MA, Hosni ES, D’Avila OP, de Figueiredo PJ. Sclerotherapy for vascular malformations in the oral and maxillofacial region: treatment and follow-up of 66 lesions. J Oral Maxillofac Surg. 2011;69:e88-92.,2020 Fowell C, Verea Linares C, Jones R, Nishikawa H, Monaghan A. Venous malformations of the head and neck: current concepts in management. Br J Oral Maxillofac Surg. 2017;55:3-9.

21 Neville B, Damm DD, Allen C, Bouquot J. Oral and maxillofacial pathology. In: 3rd ed. Philadelphia: Saunders; 2002. p. 984.

22 Cabrera J, Redondo P. Sclerosing treatment of vascular malformations. An Sist Sanit Navar. 2004;27(Suppl. 1):117-26.

23 Deveikis JP. Percutaneous ethanol sclerotherapy for vascular malformations in the head and neck. Arch Facial Plast Surg. 2005;7:322-5.

24 Kim KH, Sung MW, Roh JL, Han MH. Sclerotherapy for congenital lesions in the head and neck. Otolaryngol Head Neck Surg. 2004;131:307-16.
-2525 Hong SK, Lee HJ, Seo JK, Lee D, Hwang SW, Sung HS. Reactive vascular lesions treated using ethanolamine oleate sclerotherapy. Dermatol Surg. 2010;36:1148-52. For smaller lesions, the treatment can lead to complete remission of the lesion or a significant reduction in the size, without the need for complementary therapies.1818 Buckmiller LM, Richter GT, Suen JY. Diagnosis and management of hemangiomas and vascular malformations of the head and neck. Oral Dis. 2010;16:405-18. Among the various sclerosis-inducing agents, monoethanolamine oleate is currently the best option due to the low toxicity in comparison to other sclerosing agents.1313 Ribeiro MC, de Mattos Camargo Grossmann S, do Amaral MBF, de Castro WH, Navarro TP, et al. Effectiveness and safety of foam sclerotherapy with 5% ethanolamine oleate in the treatment of low-flow venous malformations in the head and neck region: a case series. Int J Oral Maxillofac Surg. 2018;47:900-7.,1414 Hyodoh H, Hori M, Akiba H, Tamakawa M, Hyodoh K, Hareyama M. Peripheral vascular malformations: imaging, treatment approaches, and therapeutic issues. Radiographics. 2005;25(Suppl. 1):S159-71. In addition, this type of treatment has lower odds of hemorrhage, scarring, and hyperpigmentation, besides being less invasive than surgery.11 Johann AC, Aguiar MC, do Carmo MA, Gomez RS, Castro WH, Mesquita RA. Sclerotherapy of benign oral vascular lesion with ethanolamine oleate: an open clinical trial with 30 lesions. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;100:579-84.,2525 Hong SK, Lee HJ, Seo JK, Lee D, Hwang SW, Sung HS. Reactive vascular lesions treated using ethanolamine oleate sclerotherapy. Dermatol Surg. 2010;36:1148-52.

There is still no consensus in the literature as to the ideal concentration of this sclerosing agent for the treatment of VMs.11 Johann AC, Aguiar MC, do Carmo MA, Gomez RS, Castro WH, Mesquita RA. Sclerotherapy of benign oral vascular lesion with ethanolamine oleate: an open clinical trial with 30 lesions. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;100:579-84.,77 Hoque S, Das BK. Treatment of venous malformations with ethanolamine oleate: a descriptive study of 83 cases. Pediatr Surg Int. 2011;27:527-31.,1515 Choi YH, Han MH, O-Ki K, Cha SH, Chang KH. Craniofacial cavernous venous malformations: percutaneous sclerotherapy with use of ethanolamine oleate. J Vasc Interv Radiol. 2002;13:475-82.,1616 Costa JR, Torriani MA, Hosni ES, D’Avila OP, de Figueiredo PJ. Sclerotherapy for vascular malformations in the oral and maxillofacial region: treatment and follow-up of 66 lesions. J Oral Maxillofac Surg. 2011;69:e88-92. A previous study indicated the use of monoethanolamine oleate 5% at lower doses than 1 mL per session.2626 Matsumoto K, Nakanishi H, Koizumi Y, Seike T, Kanda I, Kubo Y. Scletotherapy of hemangioma with late involution. Dermatol Surg. 2003;29:668-71. The Brazilian National Health Surveillance Agency (Agência Nacional de Vigilância Sanitária [ANVISA]; 2016) recommends a dose of 0.5-2 mL in each vein, with the total not to exceed 6 mL. In this study, 0.7 mL of monoethanolamine oleate was used at a concentration of 5% diluted in 0.3 mL of anesthetic, totaling 1 mL maximum per session in each lesion, which is the protocol used at this institution.2727 Battisti MP, Tinoco de Araújo JE, Feitosa Leitão de Oliveira T, Bonifácio da Silva Sampieri M, Damante JH, Da Silva Santos PS. Ultrasonography as a complementary exam in the diagnosis of oral arteriovenous malformation. Minerva Stomatol. 2015;64:47-52.

In 2005, Hyodoh et al. reported that a single application was sufficient for total resolution in smaller vascular lesions (≤30 mm). However, in the study, all the vascular lesions were smaller than 30 mm, but only eight cases (42%) received a single application of the sclerosing agent.1414 Hyodoh H, Hori M, Akiba H, Tamakawa M, Hyodoh K, Hareyama M. Peripheral vascular malformations: imaging, treatment approaches, and therapeutic issues. Radiographics. 2005;25(Suppl. 1):S159-71. On average, 1.6 sessions were needed for each lesion using monoethanolamine oleate at a concentration of 5% until resolution of the lesions, the same method already used in previous studies.1515 Choi YH, Han MH, O-Ki K, Cha SH, Chang KH. Craniofacial cavernous venous malformations: percutaneous sclerotherapy with use of ethanolamine oleate. J Vasc Interv Radiol. 2002;13:475-82.,1616 Costa JR, Torriani MA, Hosni ES, D’Avila OP, de Figueiredo PJ. Sclerotherapy for vascular malformations in the oral and maxillofacial region: treatment and follow-up of 66 lesions. J Oral Maxillofac Surg. 2011;69:e88-92.,2525 Hong SK, Lee HJ, Seo JK, Lee D, Hwang SW, Sung HS. Reactive vascular lesions treated using ethanolamine oleate sclerotherapy. Dermatol Surg. 2010;36:1148-52. The 5% concentration was responsible for the smaller number of sessions when compared to the study by Johann (2005), who required an average of 3.7 sessions due to the use of lower concentrations of the sclerosing agent (1.5% and 2.5%).11 Johann AC, Aguiar MC, do Carmo MA, Gomez RS, Castro WH, Mesquita RA. Sclerotherapy of benign oral vascular lesion with ethanolamine oleate: an open clinical trial with 30 lesions. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;100:579-84.

Complications in sclerotherapy are dose-dependent, and the most common one is peripheral nerve damage or skin necrosis, which can result in scars and lead to esthetic problems.1515 Choi YH, Han MH, O-Ki K, Cha SH, Chang KH. Craniofacial cavernous venous malformations: percutaneous sclerotherapy with use of ethanolamine oleate. J Vasc Interv Radiol. 2002;13:475-82.,2828 Yakes WF, Luethke JM, Parker SH, Stavros AT, Rak KM, Hopper KD, et al. Ethanol embolization of vascular malformations. Radiographics. 1990;10:787-96.

29 O’Donovan JC, Donaldson JS, Morello FP, Pensler JM, Vogelzang RL, Bauer B. Symptomatic hemangiomas and venous malformations in infants, children, and young adults: treatment with percutaneous injection of sodium tetradecyl sulfate. AJR Am J Roentgenol. 1997;169:723-9.
-3030 Munavalli GS, Weiss RA. Complications of sclerotherapy. Semin Cutan Med Surg. 2007;26:22-8. This condition occurs when an excessive amount of the sclerosing agent invades the normal tissue or when high pressure is used during the application.2525 Hong SK, Lee HJ, Seo JK, Lee D, Hwang SW, Sung HS. Reactive vascular lesions treated using ethanolamine oleate sclerotherapy. Dermatol Surg. 2010;36:1148-52.,3030 Munavalli GS, Weiss RA. Complications of sclerotherapy. Semin Cutan Med Surg. 2007;26:22-8.

Patients may also develop hemoglobinuria and hemolytic renal failure, but this is limited to doses greater than 9.6 mL of monoethanolamine oleate.3131 Miyoshi H, Oshiba S, Matsumoto A, Hayashi K, Tei H. The prophylactic effect of haptoglobin administration on renal disfunction in endoscopic injection sclerotherapy. Nihon Shokakibyo Gakkai Zasshi. 1989;86:280.,3232 Nishikawa M, Sakamoto K, Hidaka M, Yamashita A, Yamamoto G. Venous malformation of the tongue in a child treated by sclerotherapy with ethanolamine oleate: a case report. J Pediatr Surg. 2006;41:599-600. Thus, in this study, the sclerosing solution was injected with light pressure in the vascular lumen, using positive aspiration of blood to be certain of depositing the agent in the correct place to avoid or minimize complications.

Only two patients presented symptoms in the area of the VMs at the time of the initial evaluation, and all of the patients had complained of unsatisfactory esthetic appearance before treatment. Therefore, sclerotherapy was an esthetic indication for the cases treated in this study. All patients reported a burning sensation during application of the sclerosing solution, which had also been described in other studies.11 Johann AC, Aguiar MC, do Carmo MA, Gomez RS, Castro WH, Mesquita RA. Sclerotherapy of benign oral vascular lesion with ethanolamine oleate: an open clinical trial with 30 lesions. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;100:579-84.,1515 Choi YH, Han MH, O-Ki K, Cha SH, Chang KH. Craniofacial cavernous venous malformations: percutaneous sclerotherapy with use of ethanolamine oleate. J Vasc Interv Radiol. 2002;13:475-82. In addition, in 2002, Choi et al. reported burning sensation during injection even in cases in which local anesthetic was applied prior to sclerotherapy, but there were no complaints of pain during infiltration of the sclerosing agent in any of the cases.1515 Choi YH, Han MH, O-Ki K, Cha SH, Chang KH. Craniofacial cavernous venous malformations: percutaneous sclerotherapy with use of ethanolamine oleate. J Vasc Interv Radiol. 2002;13:475-82. In 2007, Bonan observed that dilution of monoethanolamine oleate in distilled water also does not reduce the symptoms; besides, it could be responsible for the decrease in action by the chemical agent on the vessel walls.3333 Bonan PR, Miranda LP, Mendes DC, de Paula AM, Pego SP, Martelli-Júnior H. Effectiveness of low flow vascular lesions sclerosis with monoetanolamine: report of six cases. Med Oral Patol Oral Cir Bucal. 2007;12:E524-7.

It was also observed and reported that after application of the sclerosing solution, there was edema that lasted from 72 h to seven days after the procedure. Other post-procedure symptoms were paresthesia in one patient (5.2%) and one case of tingling (5.2%). These signs and symptoms had resolved spontaneously by the first follow-up visit, with no need for additional therapy. No other side effects were observed in this study, and the complications rate did not differ from that of other studies.11 Johann AC, Aguiar MC, do Carmo MA, Gomez RS, Castro WH, Mesquita RA. Sclerotherapy of benign oral vascular lesion with ethanolamine oleate: an open clinical trial with 30 lesions. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;100:579-84.,77 Hoque S, Das BK. Treatment of venous malformations with ethanolamine oleate: a descriptive study of 83 cases. Pediatr Surg Int. 2011;27:527-31.,1515 Choi YH, Han MH, O-Ki K, Cha SH, Chang KH. Craniofacial cavernous venous malformations: percutaneous sclerotherapy with use of ethanolamine oleate. J Vasc Interv Radiol. 2002;13:475-82.,2525 Hong SK, Lee HJ, Seo JK, Lee D, Hwang SW, Sung HS. Reactive vascular lesions treated using ethanolamine oleate sclerotherapy. Dermatol Surg. 2010;36:1148-52.,3434 Marrocco-Trischitta MM, Nicodemi EM, Stillo F. Sclerotherapy for venous malformations of the glans penis. Urology. 2001;57:310-3.

In all the VMs (21 lesions), the application of 0.7 mL monoethanolamine oleate 5% as monotherapy was an easy, simple, quick method, well tolerated by patients, with low morbidity, since it was performed as an outpatient procedure with a limited number of sessions. Despite the small sample size and the fact that this was a retrospective study with the analysis of electronic patient files, the data showed that this is an effective method in 100% of the cases, since it showed improvement in the clinical signs and symptoms, with a subjective and objective decrease in the volume or swelling of treated VMs and thus an esthetic improvement in the region.

Conclusion

Sclerotherapy with monoethanolamine oleate 5% as monotherapy is effective, safe, and easy to apply, capable of providing excellent esthetic results within a small number of sessions, and is well accepted by patients.

  • Financial support
    This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001.
  • How to cite this article: Manzano BR, Premoli AM, Santaella NG, Ikuta CR, Rubira CM, da Silva Santos PS. Sclerotherapy as an esthetic indication in oral vascular malformations: a case series. An Bras Dermatol. 2019;94:521-6.
  • ☆☆
    Study conducted at the Graduate Studies Clinic in Stomatology and Radiology, Faculdade de Odontologia de Bauru, Universidade de São Paulo, Bauru, SP, Brazil.

References

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    Wójcicki P, Wójcicka K. Epidemiology, diagnostics and treatment of vascular tumours and malformations. Adv Clin Exp Med. 2014;23:475-84.
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    Clemens RK, Pfammatter T, Meier TO, Alomari AI, Amann-Vesti BR. Vascular malformations revisited. Vasa. 2015;44:5-22.
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    Enjolras O, Wassef M, Chapot R. Color atlas of vascular tumors and vascular malformations. New York: Cambridge University Press; 2007.
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    Johnson PL, Eckard DA, Brecheisen MA, Girod DA, Tsue TT. Percutaneous ethanol sclerotherapy of venous malformations of the tongue. AJNR Am J Neuroradiol. 2002;23:779-82.
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    Buckmiller LM. Update on hemangiomas and vascular malformations. Curr Opin Otolaryngol Head Neck Surg. 2004;12:476-87.
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Publication Dates

  • Publication in this collection
    09 Dec 2019
  • Date of issue
    Nov-Dec 2019

History

  • Received
    15 Aug 2017
  • Accepted
    26 June 2018
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