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1.
Ann Chir Plast Esthet ; 69(5): 410-418, 2024 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-39003225

RESUMO

INTRODUCTION: Breast reconstruction after cancer surgery through lipomodeling can be performed alone or in combination with a flap. Our objective is to describe the proportion of techniques used on patients who underwent autologous reconstructive surgery after tumorectomy or mastectomy in Franche-Comté. MATERIALS AND METHODS: A bicentric retrospective observational study was conducted between October 2017 and December 2021 (NCT06101732), including three groups: those who underwent exclusive lipomodeling reconstruction after mastectomy (1) or in addition to a flap (2), and those who underwent exclusive lipomodeling reconstruction after tumorectomy (3). Socio-demographic, medical, and surgical data were collected and recorded in a specially designed software. RESULTS: Two hundred and fifty-one lipomodeling procedures were performed on 91 patients. In group 1, the average transferred volume was 1191mL with an average number of sessions of 4.4 spreads over 19.4months. In group 2, the average transferred volume was 676mL with an average operative time of 2.5 spread over 16.1months. In group 3, the average transferred volume was 223mL with an average number of sessions of 1.5 spreads over 6.2months. Regarding postoperative complications, 11% had cysts of fat necrosis, 4.4% had infections, and 2.2% had hematomas. CONCLUSION: Lipomodeling is a technique that has clearly established itself in the field of breast reconstructive surgery. It results in a few complications and improves the final aesthetic outcome whether used exclusively or in addition to a flap.


Assuntos
Neoplasias da Mama , Mamoplastia , Mastectomia , Retalhos Cirúrgicos , Humanos , Mamoplastia/métodos , Feminino , Estudos Retrospectivos , Pessoa de Meia-Idade , Mastectomia/métodos , Neoplasias da Mama/cirurgia , Adulto , França , Idoso , Tecido Adiposo/transplante , Lipectomia/métodos , Complicações Pós-Operatórias/epidemiologia
2.
J Eur Acad Dermatol Venereol ; 32(2): 323-328, 2018 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-28833652

RESUMO

BACKGROUND: Bateman purpura is characterized by diffuse senile skin atrophy, senile purpura and spontaneous stellar pseudocicatrices. Cutaneous changes in the course of ageing have been related to lower levels of ascorbic acid into the dermis of elderly people. OBJECTIVE: In this study, we postulate that senile purpura could be linked to dermal vitamin C deficiency and could be corrected by topical administration of this vitamin. METHODS: A 12-weeks, hemi-member (forearm or leg), randomized double-blind comparative study was conducted in 18 patients with Bateman purpura aged over than 60 years. At each visit, clinical assessment and biometrological measurements were performed. Clinical examination and scoring by experts showed a significant improvement on the vitamin C-treated side compared with the control, with reduction of haemorrhage areas, increase of dermal thickness. RESULTS: Twice-daily application of 5% topical vitamin C led to a clinically apparent improvement of the skin symptoms and allows beneficial effects on skin elasticity and thickness. Bateman purpura, a classical sign of photoaging whose origin has not clearly been recognized could be improved by vitamin C applied on to the skin. CONCLUSION: These results confirm the hypothesis of the underlying role of vitamin C deficiency in the determinism of Bateman purpura.


Assuntos
Ácido Ascórbico/metabolismo , Ácido Ascórbico/uso terapêutico , Púrpura/metabolismo , Envelhecimento da Pele/fisiologia , Vitaminas/uso terapêutico , Administração Cutânea , Idoso de 80 Anos ou mais , Ácido Ascórbico/administração & dosagem , Deficiência de Ácido Ascórbico/complicações , Colorimetria , Método Duplo-Cego , Elasticidade , Humanos , Púrpura/etiologia , Pele/fisiopatologia , Creme para a Pele/uso terapêutico , Dobras Cutâneas , Vitaminas/administração & dosagem
7.
Rev Med Interne ; 41(3): 152-159, 2020 Mar.
Artigo em Francês | MEDLINE | ID: mdl-31980188

RESUMO

BACKGROUND: Belimumab is currently approved for the treatment of active systemic lupus erythematosus (SLE). The aim of our study was to evaluate the efficacy of belimumab in the treatment of cutaneous lupus erythematosus (CLE), resistant to conventional therapy. PATIENTS AND METHODS: Seven patients with resistant and progressive LEC and treated with belimumab were retrospectively analyzed. The efficacy and safety of belimumab were evaluated with the CLASI, RCLASI and DLQI scores, after 6 to 12 months of treatment. RESULTS: Eighty-three percent of patients demonstrated a significant clinical improvement based on the CLASI and RCLASI activity scores, including 1 complete and 4 partial responses, without worsening of CLASI and RCLASI damage scores. Eighty percent of patients also showed an improvement of their quality of life (DLQI). Oral corticosteroids were discontinued in all patients. Tolerance was acceptable with only one serious adverse event (bacteriema). CONCLUSION: Our study suggests the clinical efficiency of belimumab in a series of 7 patients presenting a resistant and progressive CLE.


Assuntos
Anticorpos Monoclonais Humanizados/uso terapêutico , Resistência a Medicamentos , Imunossupressores/uso terapêutico , Lúpus Eritematoso Cutâneo/tratamento farmacológico , Corticosteroides/uso terapêutico , Adulto , Idoso , Idoso de 80 Anos ou mais , Estudos de Coortes , Progressão da Doença , Resistência a Medicamentos/efeitos dos fármacos , Feminino , França , Humanos , Lúpus Eritematoso Cutâneo/patologia , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Resultado do Tratamento
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