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1.
Acta cir. bras ; 31(12): 774-782, Dec. 2016. tab, graf
Article in English | LILACS | ID: biblio-837658

ABSTRACT

ABSTRACT PURPOSE: To assess the capsules formed by silicone implants coated with polyurethane foam and with a textured surface. METHODS: Sixty-four Wistar albinus rats were divided into two groups of 32 each using polyurethane foam and textured surface. The capsules around the implants were analyzed for 30, 50, 70 and 90 days. Were analyzed the following parameters: foreign body reaction, granulation tissue, presence of myofibroblasts, neoangiogenesis, presence of synovial metaplasia, capsular thickness, total area and collagen percentage of type I and III, in capsules formed around silicone implants in both groups. RESULTS: The foreign body reaction was only present in the four polyurethane subgroups. The formation of granulation tissue and the presence of myofibroblasts were higher in the four polyurethane subgroups. Regarding to neoangiogenesis and synovial metaplasia, there was no statistical difference between the groups. Polyurethane group presented (all subgroups) a greater capsule thickness, a smaller total area and collagen percentage of type I and a higher percentage area of type III, with statistical difference. CONCLUSION: The use of polyurethane-coated implants should be stimulated by the long-term results in a more stable capsule and a lower incidence of capsular contracture, despite developing a more intense and delayed inflammatory reaction in relation to implants with textured surface.


Subject(s)
Animals , Female , Rats , Polyurethanes/administration & dosage , Foreign-Body Reaction/pathology , Breast Implants/adverse effects , Silicone Gels/administration & dosage , Coated Materials, Biocompatible , Implant Capsular Contracture/pathology , Surface Properties , Rats, Wistar , Breast Implantation/methods , Collagen Type I/analysis , Collagen Type III/analysis
2.
Rev. chil. pediatr ; 85(6): 720-723, dic. 2014. ilus
Article in Spanish | LILACS | ID: lil-734814

ABSTRACT

Black henna tattoos have paraphenylenediamine (PPD), which contains a product of herbal origin, which due to its molecular characteristics is capable of inducing, in susceptible individuals, a type IV hypersensitivity reaction. It clinically manifests as a contact dermatitis that usually when it disappears, scarring and hypopigmentation are left in the injured area. Objective: To describe the case of a patient with hypersensitivity to henna tattoo and to present the most relevant phenomena associated with this condition. Case report: The case of a 6 year-old patient with a black henna tattoo on his right leg, who was diagnosed with contact dermatitis probably attributed to PPD, is presented. Mometasone furoate and topical silicone gel treatment was started with good response. Conclusion: Mometasone furoate and silicone gel are a good possible therapeutic option for treating contact dermatitis caused by PPD as the dermatosis was resolved without residual lesions.


Los tatuajes de henna negra son aquellos que contienen parafenilendiamina (PPD), que contienen un producto de origen herbal, que por sus características moleculares es capaz de inducir, en individuos susceptibles, una reacción de hipersensibilidad tipo IV. Se manifiesta clínicamente como una dermatitis de contacto, que generalmente al desaparecer, persiste de manera residual una cicatriz hipertrófica e hipopigmentación en la zona lesionada. Objetivo: Describir el caso de un paciente con hipersensibilidad al tatuaje de henna, y presentar los fenómenos más relevantes asociados a esta patología. Caso clínico: Paciente de 6 años de edad, que se realizó un tatuaje con henna negra en la pierna derecha, en quien se diagnosticó posteriormente una dermatitis de contacto atribuida probablemente a la PPD. Se comenzó tratamiento con furoato de mometasona y gel de silicona con buena respuesta por vía tópica. Conclusión: El furoato de mometasona y gel de silicona son una posible opción terapéutica de utilidad para tratar la dermatitis de contacto causada por el PPD, debido a que la dermatosis se resolvió sin lesiones residuales.


Subject(s)
Child , Female , Humans , Mometasone Furoate/therapeutic use , Phenylenediamines/adverse effects , Silicone Gels/therapeutic use , Tattooing/adverse effects , Coloring Agents/administration & dosage , Coloring Agents/adverse effects , Drug Therapy, Combination , Dermatitis, Allergic Contact/drug therapy , Dermatitis, Allergic Contact/etiology , Hypersensitivity, Delayed/drug therapy , Hypersensitivity, Delayed/etiology , Mometasone Furoate/administration & dosage , Phenylenediamines/administration & dosage , Silicone Gels/administration & dosage , Treatment Outcome
3.
Journal of Korean Medical Science ; : S249-S253, 2014.
Article in English | WPRIM | ID: wpr-191054

ABSTRACT

To date, few studies have compared the effectiveness of topical silicone gels versus that of silicone gel sheets in preventing scars. In this prospective study, we compared the efficacy and the convenience of use of the 2 products. We enrolled 30 patients who had undergone a surgical procedure 2 weeks to 3 months before joining the study. These participants were randomly assigned to 2 treatment arms: one for treatment with a silicone gel sheet, and the other for treatment with a topical silicone gel. Vancouver Scar Scale (VSS) scores were obtained for all patients; in addition, participants completed scoring patient questionnaires 1 and 3 months after treatment onset. Our results reveal not only that no significant difference in efficacy exists between the 2 products but also that topical silicone gels are more convenient to use. While previous studies have advocated for silicone gel sheets as first-line therapies in postoperative scar management, we maintain that similar effects can be expected with topical silicone gel. The authors recommend that, when clinicians have a choice of silicone-based products for scar prevention, they should focus on each patient's scar location, lifestyle, and willingness to undergo scar prevention treatment.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult , Cicatrix/prevention & control , Postoperative Period , Prospective Studies , Surveys and Questionnaires , Random Allocation , Silicone Gels/administration & dosage , Surgery, Plastic/methods , Surgical Procedures, Operative/adverse effects , Wounds and Injuries/therapy
4.
Article in English | IMSEAR | ID: sea-139866

ABSTRACT

The formation of hypertrophic scars is common following healing of the burn wound, particularly in children. The face is one of the areas of the body most frequently affected by burns. Scar formation as a result of burn wounds leads to contraction of the formed granulation tissue, which causes both aesthetic and functional impairment for the patient. Scarring has major psychological and physical repercussions. Scarring on the face and visible regions of the body can be very distressing for the patient. Prevention of scars involves early and continuous use of a compressive orthesis. However, their efficacy is often limited to the facial region because of the contours of this area of body. This paper describes a clinical case of post-burn hypertrophic scars treated with silicone gel sheeting applied with pressure under custom made auto-polymerizing resin stent.


Subject(s)
Burns/complications , Child , Cicatrix, Hypertrophic/etiology , Cicatrix, Hypertrophic/therapy , Facial Injuries/complications , Female , Humans , Occlusive Dressings , Prosthodontics , Silicone Gels/administration & dosage , Stents
5.
Article in English | IMSEAR | ID: sea-45257

ABSTRACT

An open clinical trial was conducted to assess the effect of self-adhesive silicone gel sheet (SASGS) for the treatment of hypertrophic scars and keloids in Thai people. Patients were instructed to apply the SASGS to the scars as long as possible, but not less than 12 hours per day for at least 8 weeks. The subjective results of the treatment were evaluated by the patients. The scars were evaluated for color, height, weight before and after treatment at 4 and 8 weeks. Eighteen patients with 18 hypertrophic scars or keloids were recruited into the study. Their ages ranged from 6 to 33 years (mean 21 years). The average duration of the scars was 5.7 years. Twelve patients (66.67%) stated good results. All of the 18 patients wanted to continue the treatment with SASGS. Heights of the scars were reduced in 12 lesions (66.67%) after treatment for 8 weeks (P = 0.058). Weights of the lesions were decreased in 10 lesions (55.55%) but were not statistically different (P = 0.090). Seven lesions (36.84%) were improved in color. Two patients (11.11%) developed erythematous rash around the lesions which subsided after withdrawal of the treatment. The long term follow-up for the recurrence and the mechanism of action of this treatment should be studied further.


Subject(s)
Administration, Topical , Adolescent , Adult , Child , Cicatrix, Hypertrophic/drug therapy , Drug Administration Schedule , Female , Follow-Up Studies , Humans , Keloid/drug therapy , Male , Prospective Studies , Silicone Gels/administration & dosage , Treatment Outcome
6.
Rev. chil. dermatol ; 16(1): 42-6, 2000. ilus, tab
Article in Spanish | LILACS | ID: lil-274563

ABSTRACT

Con la finalidad de prevenir o mejorar la apariencia de las cicatrices hipertróficas, sean éstas de origen quirúrgico o traumático, se ha desarrollado una gran variedad de tratamientos, tanto tópicos como sistémicos. Estas lesiones son notoriamente recurrentes y su manejo es poco satisfactorio. Ninguna medida en forma individual ha probado ser efectiva en evitar el proceso de la cicatrización hipertrófica (CH), con excepción tal vez de la silicona. El presente trabajo tiene como objetivo revisar la evidencia disponible en estudios prospectivos, controlados, descritos en la literatura acerca de la utilidad de la silicona en el tratamiento de las cicatrices hipertróficas


Subject(s)
Humans , Male , Female , Cicatrix, Hypertrophic/therapy , Silicone Gels/therapeutic use , Cicatrix, Hypertrophic/pathology , Cicatrix, Hypertrophic/prevention & control , Silicone Gels/administration & dosage , Silicone Gels/pharmacology
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