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1.
Acta Derm Venereol ; 97(5): 632-638, 2017 May 08.
Artigo em Inglês | MEDLINE | ID: mdl-28127620

RESUMO

Psoriasis has major physical, psychological, and social impacts: its management should not be restricted by individual financial considerations in Western countries as these have well-structured health systems and social/insurance coverage. We investigated if the socioeconomic characteristics of patients were associated with severity of psoriasis and access to healthcare. In a cross-sectional study, we included 903 patients with psoriasis that were consulting for the first time. We showed that low educational level was associated with severity of disease in multivariate analyses. Moreover, patients of lower class and lower educational level, with severe psoriasis, had seen fewer physicians and had less frequently received a systemic treatment. Thus, physicians need to be vigilante of patients with a low socioeconomic status. Both low socioeconomic status and less access to dermatologists are associated with clinical severity of psoriasis at a first consultation.


Assuntos
Dermatologia , Acessibilidade aos Serviços de Saúde , Disparidades em Assistência à Saúde , Psoríase/epidemiologia , Encaminhamento e Consulta , Fatores Socioeconômicos , Adulto , Distribuição de Qui-Quadrado , Estudos Transversais , Escolaridade , Feminino , França , Humanos , Masculino , Pessoa de Meia-Idade , Análise Multivariada , Psoríase/diagnóstico , Psoríase/terapia , Fatores de Risco , Índice de Gravidade de Doença
3.
Ann Biol Clin (Paris) ; 71(3): 333-7, 2013.
Artigo em Francês | MEDLINE | ID: mdl-23747671

RESUMO

Hyper-IgG4 syndrome is a rare entity characterized by fibro-inflammatory lesions of organs, an excess of IgG4 positive plasma cells in histology and high serum level IgG4. Many organs can be affected (pancreas, kidney, salivary glands) and the list continues to grow. The skin damage is rarely reported in the literature and is usually associated with other typical lesions of this syndrome. We report the case of a 53-year-old female followed since 2005 for lymphadenopathy, associated with axillary nodular skin lesions. The assessments made at that time had retained the diagnosis of pseudolymphoma with implementation of multi-line therapy. Six years later, and the persistence of the lesions, plasma cells marked by anti-IgG4 and the serum IgG4 has attached injuries to the syndrome hyper-IgG4. The patient is treated with low dose corticosteroids with a good and protacted response. Cutaneous pseudolymphoma could be a new presentation of the syndrome of hyper-IgG4 in the absence of any other injury usually associated with this entity. This case illustrates the interest for proposing a plasma cell labeling with anti-IgG4 in any case of cutaneous pseudolymphoma.


Assuntos
Hipergamaglobulinemia/diagnóstico , Imunoglobulina G/sangue , Pseudolinfoma/diagnóstico , Dermatopatias/diagnóstico , Diagnóstico Diferencial , Feminino , Humanos , Hipergamaglobulinemia/sangue , Doenças Linfáticas/sangue , Doenças Linfáticas/diagnóstico , Pessoa de Meia-Idade , Pseudolinfoma/etiologia , Dermatopatias/etiologia , Síndrome
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