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Assesment of the treatment of earlobe keloids with triamcinolone injections, surgical resection, and local pressure

Abstracts

OBJECTIVE:

To evaluate the combined treatment of ear lobe keloids.

METHODS:

We studied 46 consecutive patients with 81 ear lobe keloids. Patients underwent local infiltration of triamcinolone acetonide (TCN) at concentrations of 40mg/ml (Group 1), 20 mg/ml (Group 2) and 10mg/ml (Group 3). The volume of TCN infiltrate varied according to the size of the lesion. Treatment consisted of three monthly injections before surgery, excision of keloid in the fourth month and perioperative infiltration, followed by two more leaks TCN within two months. Patients used earrings pressure on the scar after operation for four months. The pressure exerted by earrings in the ear lobe was measured electronically. Post-treatment follow-up of patients was 24 months.

RESULTS:

TCN at concentrations of 20mg/ml and 40mg/ml were effective for the treatment of keloids, no difference between the groups (p = 0.58). However, patients in which TCN was infiltrated the 10mg/ml had poor involution of keloid and the study of this group was stopped.

CONCLUSION:

the combination of infiltration TCN month to 20 mg/mL (1.2mg to 2.0mg per mm33. Bettinger DA, Yager DR, Diegelmann RF, Cohen IK. The effect of TGF-beta on keloid fibroblast proliferation and collagen synthesis. Plast Reconstr Surg. 1996;98(5):827-33. TCN injury), surgical excision and pressure application device is effective for treatment of keloid ear lobe.

Keloid; Triamcinolone Acetonide; Wound Healing; Surgical Procedures, Operative


OBJETIVO:

avaliar o tratamento combinado do queloide do lóbulo da orelha.

MÉTODOS:

Foram estudados 46 pacientes consecutivos com 81 queloides de lóbulo da orelha. Os pacientes submeteram-se a infiltração local de triancinolona acetonida (TCN) nas concentrações de 40mg/ml (Grupo 1), 20mg/ml (Grupo 2) e 10mg/ml (Grupo 3). O volume de TCN infiltrado variou de acordo com o tamanho da lesão. O tratamento consistiu em três infiltrações mensais no pré-operatório, exérese do queloide no quarto mês e infiltração peroperatória, seguida de mais duas infiltrações de TCN nos dois meses seguintes. Os pacientes usaram brincos de pressão sobre a cicatriz após a operação durante quatro meses. A pressão exercida pelos brincos no lóbulo da orelha foi aferida eletronicamente. O seguimento pós-tratamento dos pacientes foi 24 meses.

RESULTADOS:

A TCN nas concentrações de 20mg/ml e 40mg/ml foram eficazes para o tratamento do queloide, sem diferença entre si (p=0,58). No entanto, os pacientes nos quais a TCN foi infiltrada a 10mg/ml não tiveram involução satisfatória do queloide e o estudo desse grupo foi interrompido.

CONCLUSÃO:

A combinação de infiltração mensal de TCN a 20mg/ml (1,2mg a 2,0mg de TCN por mm3 de lesão), exérese cirúrgica e aplicação de dispositivo de pressão é eficaz para tratamento do queloide de lóbulo da orelha.

Queloide; Triancinolona Acetonida; Cicatrização; Operação Cirúrgica


INTRODUCTION

The a wound repair process covers a wide spectrum of results, from the absence of healing to exuberant scarring. The mechanism of regulation of anomalous healing is not known; nor is the part or parts of the process in which lies the disorder that keeps the scar on inflammatory and proliferative phase. Keloids are scars that respond in an exaggerated way to a skin lesion, pushing the boundaries of the original wound and invading the normal skin, appearing about three months after trauma, and not regressing spontaneously, being a characteristic of humans. The main complaints are pain, itching of uncertain etiology and great aesthetic discomfort. The incidence of keloids in people with black skin ranges from 4.5% to 16%, approximately 15 times more than in whites. Its incidence is higher in between ten and 30 years of age11. Urioste SS, Arndt KA, Dover JS. Keloidal scars and hypertrophic scars: review and treatment strategies. Semin Cutan Med Surg. 1999;18(2):159-71., with no preference between genders.

Keloids are multifactorial, relating with physical, chemical, biological and endogenous agents. There seems to be a genetic predisposition, with exacerbated immune response related to emotional factors. Fibroblasts derived from keloids have an increased expression of the p6322. De Felice B, Ciarmiello LF, Mondola P, Damiano S, SeruR, Argenziano C, et al. Differential p63 and p53 expression in human keloid fibroblast and hypertrophic scar fibroblasts. DNA Cell Biol. 2007;26(8):541-7. gene, with increased response to the organic stimuli involved in wound healing. The beta transforming growth factor (TGF-b1) is also high in keloids33. Bettinger DA, Yager DR, Diegelmann RF, Cohen IK. The effect of TGF-beta on keloid fibroblast proliferation and collagen synthesis. Plast Reconstr Surg. 1996;98(5):827-33..

Corticosteroid therapy is considered the best treatment for keloids1.4. Triamcinolone (TCN) in keloids has been used since 1965 due to its efficacy66. Babin RW, Ceilley RI. The freeze-injection method of hypertrophic scar and keloid reduction. Otolaryngol Head Neck Surg. 1979;87(6):911-4.. The mechanism by which intradermal TCN actson the injury is not fully elucidated. Its greatest effect is in the inflammatory and proliferativephase, interfering in local erythema and edema resulting from capillary dilation. There is evidence of its effect on the phagocytic activity of macrophages and modulation of the fibroblasts function in collagen synthesis.

The therapeutic objective depends on the patient'ssymptoms and aesthetic complaints caused by the keloid. Although the literature on the subject is wide, there is still no effectiveness-established treatment for keloid cure. This paper presents the authors' experience evaluating the combined approach consisted of application of TCN, surgical resection, and compression to treat earlobe keloids.

METHODS

We studied 46 patients with 81 keloids, primary and recurrent, located in the earlobe. All keloids were caused by piercing injury for earring placement (Figure 1). Patients aged under 14 years and those with skin infections were not included.

Figure 1 -
Earlobe keloid before treatment.

This prospective study was approved by the Ethics Committee and Research, Department of Surgery, Faculty of Medicine and the Ethics Committee on Human Research (COEP) of UFMG, under number 133/07.

To determine the optimal dose of TCN in the treatment of keloids, the patients were divided into three groups to receive different drug concentrations: Group 1 (40mg/ml), consisting of 20 patients with 33 keloids; Group 2 (20mg/mL), consisting of 16 patients with28 keloids; and Group 3 (10mg/ml), formed by 10 patients with 20 keloids. The amount of TCN injected into the base of the lesion is proportional to the volume of the keloid. We injected 0.05ml to 0.1ml TCN per mm³ of keloid monthly for three months (Figure 2).

Figure 2 -
Perioperative infiltration followed by injury excision.

We recorded volumes of keloids (V) in cubic millimeters (mm³) in the preoperative phase with a digital caliper. The diameter and height of the lesions (D) were measured, and the volumetric calculation resulted from the following equation: average of diameter and height cubed, multiplied by the value of pi (3.14) and divided by six.

In the fourth month, the patients underwent excision of the keloid followed by TCN injection into the open area of the wound edges, using the same volume injected earlier. The wound was sutured with monofilament 5-0 nylon. All procedures were performed under local anesthesia with lidocaine injected into the keloid. After the suture, a pressureearring was applied (Figure 3A), coated with allergenic cotton knit on the scar (Figure 3B), and kept for four months, 18 hours a day.

Figure 3 -
Pressure earrings. A) Detail; B) on the spot, coated with hypoallergenic material, cotton knit.

The pressure exerted by the earrings, of 30mmHg, was measured in the Technological Centre Foundation - Physical Tests Sector, at the Universidade Federal de Minas Gerais, through the universal electromechanical testing machine.

To verify the effectiveness of the treatment, patients were followed for at least one year after the last dose of corticosteroids (Figure 4). To assess the best dose of TCN to be injected, we considered as therapeutic success no recurrence of the injury after removal and infiltration of corticosteroids. We compared the number of relapses in all three groups. We considered relapse when there was scar growth beyond the limits of the wound at the end of treatment, combined with complaints of itching and pain.

Figure 4 -
Aspect of the earlobe after treatment.

Two variables were considered together, as each indicates failure in the treatment of keloids. The statistical analysis took into account the patient's symptoms (pain and itching), and changes in the morphological characteristics of the lesion, such as stiffness and volume change, and the second variable took into account recurrence. We used the chi-square test with Fisher correctionfor statistical analysis.

RESULTS

In Group 1 (TCN to 40mg/ml) two of the 20 subjects (10%) experienced an anaphylactic reaction after the second infiltration. There was general malaise, lip swelling, flushing, dry cough, abdominal pain, symptoms that improved after intravenous administration of 1000 ml of physiological saline. Only in this group there was a whitish deposit of TCN at the time of resection of the keloid, but with no clinical significance. There were two keloid recurrences in less than one year (6%).

In Group 2 (TCN 20 mg / ml), one patient (6.2%) had anaphylactic reactions to TCN after the third infiltration. There was wound infection in one patient, treated with cephalexin for ten days without modification of the therapeutic result, considered optimal. There was one recurrence of keloid in less than one year (4.5%).

In Group 3 (TCN to 10 mg / ml), three patients maintained itching complaint until the third dose and showed no injury improvement. In two other patients, there was lesion growth. These adverse events occurred in 50% of patients, rendering unacceptable the continuation of this TCN dose. Treatment was discontinued and all patients in this group resumed treatment as set for Group 2. These patients were not relocated in Group 2. Thus, the group 3 was not part of the final analysis and statistical work.

There was no difference in the evolution of the symptoms and scar appearance between the groups that received 20mg/ml and 40mg/ml. After the third infiltration, all patients were asymptomatic and their injuries did not progress. There was improvement in scar stiffness and size regression. There was no difference (p = 0.58) between the results obtained with patients undergoing infiltration of 40mg/ml and 20mg/mlTCN.

DISCUSSION

Even a thorough review of the literature does not allow precise analysis of the results proclaimed. Some causes of this difficulty are: lack of homogeneity description and characterization of anomalous scars; statistical methodology used; limited number of patients; insufficient follow-up; and different criteria used to define relapse.

Treatment of keloids is based on three types of potential medical intervention, and they act in the complex cascade of events leading to wound healing: manipulation of the intrinsic properties of wound synthesis process; correction of the balance between normal physiological and abnormal collagen synthesis, and in its regulatory humoral factors; modification of various immune and inflammatory responses that occur during the healing process. Therapeutic modalities include, in most cases: compression of the keloid, cryosurgery, application of silicone plates, operative excision followed or not by radiotherapy, isolated radiotherapy, laser application, and intralesional injection of corticosteroids.

Keloidcompression is based on collagenfragmentation and fibroblast degradation, the minimum effective pressure for this purpose being greater than 24mmHg, so as to exceed the capillary pressure77. Sawada Y, Sone K. Hydration and occlusion treatment for hypertrophic scars and keloids. Br J Plast Surg. 1992;45(8):599-603.. We present a device developed by us, which was applied to the ear lobe, but of difficult usage in other parts of the body. Cryotherapy lends itself to treat minor injuries in leucodermas, by leading to keloid cold ischemia and possible volumetric reduction of the lesion88. Shepherd JP, Dawber RP. The response of keloid scars to cryosurgery. Plastic Reconstr Surg. 1982;70(6):677-82.. This limitation has been overcome in part by applying plates of soft silicone, which improve the hydration of the lesion, eventual improvement in the color of the lesion and surrounding skin, and increased tolerance to keloidcompression99. Linares HA, Larson DL, Willis-Galstaun BA. Historical notes on the use of pressure in the treatment of hypertrophic scars or keloids. Burns. 1993;19(1):17-21.. Radiotherapy is used usually after surgical excision. The keloid is the benign lesion most often treated by radiotherapy1010. Botwood N, Lewanski C, Lowdell C. The risks of treating keloids with radiotherapy. Br J Radiol. 1990;72(864):1222-4., which was first used in 1906. The betatherapy is the most frequently used ionizing radiation mode1111. Darzi MA, Chowdri NA, Kaul SK, Khan M. Evolution of various methods of treating keloids and hypertrophic scars: a 10-year follow-up study. Br J Plast Surg. 1992;45(5):374-9.. However, it is known for its carcinogenic potential, contraindication in children, and it's side effects on scars and keloids, such as atrophy, hypopigmentation, and skin necrosis. The LASER (Light Amplification by Stimulated Emission of Radiation), has shown good results in the treatment of keloids. It acts by modulating the anomalous tissue growth, but the results depend on the type of laser, exposure time and location of the keloid1212. Abergel RP, Meeker CA, Oikarinen H, Oikarinen AI, UittoJ. Retinoid modulation of connective tissue metabolism in keloid fibroblast cultures. Arch Dermatol. 1985;121(5):632-5.. The isolated surgical removal entails risk of recurrence, ranging from 45% to 100% of the cases, and should never be used in monotherapy1313. Shaffer JJ, Taylor SC, Cook-Bolden F. Keloidal scars: a review with a critical look at therapeutic options. J Am Acad Dermatol. 2002;46(2 Suppl Understanding):S63-97..

Among the intralesional corticosteroids, the preferred drug is triamcinolone (TCN). Although there are studies on general aspects and treatment of keloids, the best concentration and TCN dose for treatment has not yet been determined. The concentrations proposals in the literature range from 10mg/ml to 40mg/ml and the total dose, up to 120mg55. Griffith BH, Monroe CW, McKinney P. A follow-up study on the treatment of keloids with triamcinolone acetonide. Plast Reconstr Surg. 1970;46(2):145-50.. TCN is the only drug approved for keloid treatment by the Food and Drug Administration (FDA), USA. It's topical use, however, is ineffective to treat keloids.

The infiltration of TCN at the base of keloid is intended to act in the place of the mediators of the healing process and of the fibroblasts with greater replicative capacity. The retention of the drug in small volumes in the scar site reduces its systemic effects. In this study, the total dose infiltrated in keloids was lower than that found in the literature, and yet, therapeutic success was obtained in almost all patients.

Anaphylactic reactions using TCN are well documented. Corticosteroids are paradoxically responsible for anaphylactic type 1 reactions, mediated by IgE antibodies. The allergens may be the steroids themselves or the liquid used in the solution, usually carboxymethylcellulose1414. 16. Cosman B, Wolff M. Correlation of keloid recurrence with completeness of local excision. A negative report. Plast Reconstr Surg. 1972;50(2):163-6. and succinate1515. 17. Patterson DL, Yunginger JW,Dunn WF, Jones RT, Hunt LW. Anaphylaxis induced by carboxymethylcellulose component of injectable triamcinolone. Ann Allergy Asthma Immunol. 1995;74(2):163-6..

Compression of the keloid is an already establishedmethod to improve the quality of the scar88. Shepherd JP, Dawber RP. The response of keloid scars to cryosurgery. Plastic Reconstr Surg. 1982;70(6):677-82.. Nevertheless, there is no publication on the pressure intensity that must be performed in the scar. In this study, we used the higher pressure bearable in all patients, without discomfort.

The development of stem cell research1616. 19. Tuan TL, Nichter LS. The molecular basis of keloid and hypertrophic scar formation. Mol Med Today. 1998;4(1):19-24. has helped to elucidate the balance of formation and cellular remodeling activity. It is described that flags (cytokines), molecular alterations in receptor cytoplasmic membrane of fibroblasts and genetic mutations alter the healing process1717. 20. Kim WJ. Cellular signaling in tissue regeneration. Yonsei Med J. 2000;41(6):692-703.. Growth factors are important in the modulation of various cellular activities1818. 21. Lee TY, Chin GS, Kim WJ, Chau D, GittesGK, Longaker MT. Expression of transforming growth factor beta 1, 2, and 3 proteins in keloids. Ann Plast Surg. 1999;43(2):179-84.. New therapeutic strategies to enhance wound healing and promote the formation of healthy scars are currently being studied, using anti-TGF-â antibodies.

TCN infiltration at a concentration of 20mg / ml in combination with the scar removal and compression earring is effective and sufficient to treat earlobe keloids. The administration of lower doses of corticosteroids is insufficient, and higher doses are unnecessary to obtain good therapeutic results.

REFERENCES

  • 1
    Urioste SS, Arndt KA, Dover JS. Keloidal scars and hypertrophic scars: review and treatment strategies. Semin Cutan Med Surg. 1999;18(2):159-71.
  • 2
    De Felice B, Ciarmiello LF, Mondola P, Damiano S, SeruR, Argenziano C, et al. Differential p63 and p53 expression in human keloid fibroblast and hypertrophic scar fibroblasts. DNA Cell Biol. 2007;26(8):541-7.
  • 3
    Bettinger DA, Yager DR, Diegelmann RF, Cohen IK. The effect of TGF-beta on keloid fibroblast proliferation and collagen synthesis. Plast Reconstr Surg. 1996;98(5):827-33.
  • 4
    Ketchum LD, Robinson DW, Masters FW. Follow-up on treatment of hypertrophic scars and keloids with triamcinolone. Plast Reconstr Surg. 1971;48(3):256-9.
  • 5
    Griffith BH, Monroe CW, McKinney P. A follow-up study on the treatment of keloids with triamcinolone acetonide. Plast Reconstr Surg. 1970;46(2):145-50.
  • 6
    Babin RW, Ceilley RI. The freeze-injection method of hypertrophic scar and keloid reduction. Otolaryngol Head Neck Surg. 1979;87(6):911-4.
  • 7
    Sawada Y, Sone K. Hydration and occlusion treatment for hypertrophic scars and keloids. Br J Plast Surg. 1992;45(8):599-603.
  • 8
    Shepherd JP, Dawber RP. The response of keloid scars to cryosurgery. Plastic Reconstr Surg. 1982;70(6):677-82.
  • 9
    Linares HA, Larson DL, Willis-Galstaun BA. Historical notes on the use of pressure in the treatment of hypertrophic scars or keloids. Burns. 1993;19(1):17-21.
  • 10
    Botwood N, Lewanski C, Lowdell C. The risks of treating keloids with radiotherapy. Br J Radiol. 1990;72(864):1222-4.
  • 11
    Darzi MA, Chowdri NA, Kaul SK, Khan M. Evolution of various methods of treating keloids and hypertrophic scars: a 10-year follow-up study. Br J Plast Surg. 1992;45(5):374-9.
  • 12
    Abergel RP, Meeker CA, Oikarinen H, Oikarinen AI, UittoJ. Retinoid modulation of connective tissue metabolism in keloid fibroblast cultures. Arch Dermatol. 1985;121(5):632-5.
  • 13
    Shaffer JJ, Taylor SC, Cook-Bolden F. Keloidal scars: a review with a critical look at therapeutic options. J Am Acad Dermatol. 2002;46(2 Suppl Understanding):S63-97.
  • 14
    16. Cosman B, Wolff M. Correlation of keloid recurrence with completeness of local excision. A negative report. Plast Reconstr Surg. 1972;50(2):163-6.
  • 15
    17. Patterson DL, Yunginger JW,Dunn WF, Jones RT, Hunt LW. Anaphylaxis induced by carboxymethylcellulose component of injectable triamcinolone. Ann Allergy Asthma Immunol. 1995;74(2):163-6.
  • 16
    19. Tuan TL, Nichter LS. The molecular basis of keloid and hypertrophic scar formation. Mol Med Today. 1998;4(1):19-24.
  • 17
    20. Kim WJ. Cellular signaling in tissue regeneration. Yonsei Med J. 2000;41(6):692-703.
  • 18
    21. Lee TY, Chin GS, Kim WJ, Chau D, GittesGK, Longaker MT. Expression of transforming growth factor beta 1, 2, and 3 proteins in keloids. Ann Plast Surg. 1999;43(2):179-84.
  • Source of funding: no

Publication Dates

  • Publication in this collection
    Jan-Feb 2015

History

  • Received
    02 Feb 2014
  • Accepted
    18 Apr 2014
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