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Scleroderma en coup de sabre treated with polymethylmethacrylate - Case report* * Work carried out at the Hospital Universitário Gafrée e Guinle, Universidade Federal do Estado do Rio de Janeiro (HUGG-UNIRIO) – Rio de Janeiro (RJ), Brazil.

Abstract

The scleroderma en coup de sabre is a variant of localized scleroderma that occurs preferentially in children. The disease progresses with a proliferative and inflammatory phase and later atrophy and residual deformity, which are treated with surgical techniques such as injectable fillers, transplanted or autologous fat grafting and resection of the lesion. Among the most widely used fillers is hyaluronic acid. However, there are limitations that motivate the search for alternatives, such as polymethylmethacrylate, a permanent filler that is biocompatible, non-toxic, non-mutagenic and immunologically inert. In order to illustrate its application, a case of scleroderma en coup de sabre in a 17-year-old patient, who was treated with polymethylmethacrylate with excellent aesthetic results, is reported.

Keywords:
Atrophy; Cicatrix; Cosmetic techniques; Polymethyl methacrylate; Scleroderma, localized

INTRODUCTION

The scleroderma en coup de sabre is a variant of linear or localized scleroderma that occurs preferentially in children. It may involve all of the hemiface, extending from the scalp to the the nose, lips and tongue.11 Choksi AN, Orringer JS. Linear morphea-induced atrophy treated with hyaluronic acid filler injections. Dermatol Surg. 2011;37:880-3.,22 Duarte AA. Colagenoses e a dermatologia. 2 ed. Rio de Janeiro: Di Livros; 2012. Its etiology is unknown, but probably it is of autoimmune nature.11 Choksi AN, Orringer JS. Linear morphea-induced atrophy treated with hyaluronic acid filler injections. Dermatol Surg. 2011;37:880-3.,33 Burns T, Breathnach S, Cox N, Griffiths, editors. Rook's textbook of dermatology. 8th ed. New York: Blackwell Science; 2010.,44 Zancanaro PCQ, Isaac AR, Garcia LT, Costa IMC. Localized scleroderma in children: clinical, diagnostic and therapeutic aspects. An Bras Dermatol. 2009;84:161-72. Besides the skin lesions, neurologic and ophthalmologic abnormalities may occur. There may be cicatricial alopecia (scarring hair loss), hyperchromic and depressed residual lesions.22 Duarte AA. Colagenoses e a dermatologia. 2 ed. Rio de Janeiro: Di Livros; 2012.

The treatment for localized scleroderma consists of inhibition of the proliferative and inflammatory phase of the disease, which is done by means of oral medication like corticosteroids, cyclophosphamide, methotrexate, cyclosporine, pentoxifylline and penicillamine, among others, as well as topical medication, such as corticosteroids, tacrolimus, pimecrolimus and colchicine.44 Zancanaro PCQ, Isaac AR, Garcia LT, Costa IMC. Localized scleroderma in children: clinical, diagnostic and therapeutic aspects. An Bras Dermatol. 2009;84:161-72. In the phase of residual atrophy and deformity, the treatment of choice is done with surgical techniques such as injectable fillers, transplanted or autologous fat grafting and resection of the lesion.11 Choksi AN, Orringer JS. Linear morphea-induced atrophy treated with hyaluronic acid filler injections. Dermatol Surg. 2011;37:880-3.,22 Duarte AA. Colagenoses e a dermatologia. 2 ed. Rio de Janeiro: Di Livros; 2012.

Among the fillers, the most widely used is the hyaluronic acid, a hygroscopic, absorbable gel.55 Beasley KL, Weiss MA, Weiss RA. Hyaluronic acid fillers: a comprehensive review. Facial Plast Surg. 2009;25:86-94. However, limitations like durability and cost of the filler are factors that lead to the search for other alternatives. We report a case of scleroderma en coup de sabre treated with polymethylmethacrylate (PMMA), with the objective of illustrating a little-used option.

CASE REPORT

Male patient, 14-year-old, with scleroderma en coup de sabre for 6 years. There was no neurologic or ophthalmologic abnormality. The examination revealed an atrophic and depressed lesion that extended from the forehead to the scalp, with alopecia. At first he was treated with colchicine ointment, clobetasol cream and intralesional triamcinolone. Three years after the skin lesion became stable the PMMA filling was done in 3 sessions, with a 3-month interval between sessions. The procedure was started after the custodial person was informed about possible complications and signed a consent form.

PMMA 10% was used in the forehead with retroinjections in thin cylinders, crossed in X with the purpose of raising the skin, maintaining flexibility without adding too much volume (Figure 1). In the scalp, PMMA 30% was used with retroinjections in thicker cylinders, forming a network to produce more volume. After the treatment, we observed raising of the depressed portion and partial hair regrowth in the alopecia area of the scalp (Figure 2). When inquired about the degree of satisfaction regarding the result of the treatment in a zero to ten scale, the patient answered nine.

Figure 1
Patient before (A) and after (B) the third A session of PMMA at 10% in the frontal region

Figure 2
Patient before (A) and after (B) the third session of PMMA at 30% in the scalp

DISCUSSION

The scleroderma en coup de sabre is a type of linear scleroderma that may produce disfiguring scars. There are some surgical therapeutic options for the treatment of residual atrophy.11 Choksi AN, Orringer JS. Linear morphea-induced atrophy treated with hyaluronic acid filler injections. Dermatol Surg. 2011;37:880-3. Among them are injectable fillers (hyaluronic acid, PMMA, calcium hydroxylapatite), transplanted or autologous fat grafting and resection of the lesion.11 Choksi AN, Orringer JS. Linear morphea-induced atrophy treated with hyaluronic acid filler injections. Dermatol Surg. 2011;37:880-3.

It is important to emphasize that injectable fillers should only be used when the skin lesion is stable, that is, without growth or alterations in consistency or skin color. However, the patient should be warned that the treatment does not prevent from a possible relapse to the proliferative phase, since disease activity lasts around 3 to 5 years and may extend up to 25 years, with an uncertain progression time.22 Duarte AA. Colagenoses e a dermatologia. 2 ed. Rio de Janeiro: Di Livros; 2012.,33 Burns T, Breathnach S, Cox N, Griffiths, editors. Rook's textbook of dermatology. 8th ed. New York: Blackwell Science; 2010.

We chose PMMA because it is a permanent filler, biocompatible, not toxic, non-mutagenic and immunologically inert. PMMA does not require a previous cutaneous test as its microspheres are 100% polymerized. Therefore, allergies are rare.66 Carvalho Costa IM, Salaro CP, Costa MC. Polymethylmethacrylate facial implant: a successful personal experience in Brazil for more than 9 years. Dermatol Surg. 2009;35:1221-7. We use it in 10% and 30% concentrations.22 Duarte AA. Colagenoses e a dermatologia. 2 ed. Rio de Janeiro: Di Livros; 2012. Besides these advantages, one of the factors that made us choose the product was its ready availability at our service, since the patient did not have the means to purchase the medication.

After a PMMA application, there is a reaction of foreign body type that induces the onset of giant cells that wrap each particle of the product, leading to new collagen and blood vessels formation. That means that the defect is corrected by the volume of the product added and the incorporation of cells and collagen fibers that appear at the site.77 Sandoval MHL, Ayres EL. Preenchedores: Guia Prático de Técnicas e Produtos. São Paulo: AC Farmacêutica; 2013.

According to the instructions accompanying the product, PMMA is recommended for facial and body volume correction and also to correct lipodistrophy caused by use of antiretrovirals in patients with HIV.88 Serra MS, Oyafuso LK, Trope BM, Munhoz Leite OH, Ramos-e-Silva M. An index for staging facial lipoatrophy and evaluation of the efficacy of the treatment with polymethylmethacrylate in HIV/AIDS patients: a pilot study. J Eur Acad Dermatol Venereol. 2013;27:990-6. Its use has also been reported for treatment of acne scars and facial lipoatrophy induced by cutaneous lupus panniculitis.88 Serra MS, Oyafuso LK, Trope BM, Munhoz Leite OH, Ramos-e-Silva M. An index for staging facial lipoatrophy and evaluation of the efficacy of the treatment with polymethylmethacrylate in HIV/AIDS patients: a pilot study. J Eur Acad Dermatol Venereol. 2013;27:990-6.

Based on this information and the result obtained for the patient described, PMMA filling is a good therapeutic option for esthetic improvement of residual scarring following scleroderma and an alternative to avoid more invasive surgical procedures.

  • Financial Support: None.
  • *
    Work carried out at the Hospital Universitário Gafrée e Guinle, Universidade Federal do Estado do Rio de Janeiro (HUGG-UNIRIO) – Rio de Janeiro (RJ), Brazil.

REFERENCES

  • 1
    Choksi AN, Orringer JS. Linear morphea-induced atrophy treated with hyaluronic acid filler injections. Dermatol Surg. 2011;37:880-3.
  • 2
    Duarte AA. Colagenoses e a dermatologia. 2 ed. Rio de Janeiro: Di Livros; 2012.
  • 3
    Burns T, Breathnach S, Cox N, Griffiths, editors. Rook's textbook of dermatology. 8th ed. New York: Blackwell Science; 2010.
  • 4
    Zancanaro PCQ, Isaac AR, Garcia LT, Costa IMC. Localized scleroderma in children: clinical, diagnostic and therapeutic aspects. An Bras Dermatol. 2009;84:161-72.
  • 5
    Beasley KL, Weiss MA, Weiss RA. Hyaluronic acid fillers: a comprehensive review. Facial Plast Surg. 2009;25:86-94.
  • 6
    Carvalho Costa IM, Salaro CP, Costa MC. Polymethylmethacrylate facial implant: a successful personal experience in Brazil for more than 9 years. Dermatol Surg. 2009;35:1221-7.
  • 7
    Sandoval MHL, Ayres EL. Preenchedores: Guia Prático de Técnicas e Produtos. São Paulo: AC Farmacêutica; 2013.
  • 8
    Serra MS, Oyafuso LK, Trope BM, Munhoz Leite OH, Ramos-e-Silva M. An index for staging facial lipoatrophy and evaluation of the efficacy of the treatment with polymethylmethacrylate in HIV/AIDS patients: a pilot study. J Eur Acad Dermatol Venereol. 2013;27:990-6.

Publication Dates

  • Publication in this collection
    Mar-Apr 2016

History

  • Received
    22 July 2014
  • Accepted
    04 Nov 2014
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