Navegando por Palavras-chave "Lupus erythematosus"

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    Coexistence of chronic cutaneous lupus erythematosus and frontal fibrosing alopecia
    (Soc Brasileira Dermatologia, 2018) Nascimento, Luciana Lima do [UNIFESP]; Enokihara, Milvia Maria Simões e Silva [UNIFESP]; Vasconcellos, Monica Ribeiro de Azevedo [UNIFESP]
    Lupus erythemathosus is a chronic, relapsing disease with acute, subacute, and chronic lesions. Effluvium telogen occurs in the setting of systemic activity of the disease, and cicatricial alopecia results from discoid lesionsin on the scalp. Other types of alopecia, like alopecia areata, may rarely be found in lupus. Frontal fibrosing alopecia is characterized by frontotemporal hairline recession and eybrow loss. Histophatologically, it cannot be differentiated from lichen planopilaris. It is controversial whether frontal fibrosing alopecia is a subtype of lichen planopilaris.. A pacient with chronic lichenoid lupus erythematosus is described with clinical, histophatological and dermoscopic features of frontal fibrosing alopecia. We have not been able to find in the literature cases of frontal fibrosing alopecia as a clinical manifestation of lupus.
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    Lúpus eritematoso sistêmico bolhoso associado à nefrite lúpica: relato de dois casos
    (Sociedade Brasileira de Dermatologia, 2007-02-01) Cato, Ellen Erie; Lima, Alciara De Sousa; Pontes, Alexandre L. Lourenço; Vannucci, Andrea Barranjard; Levites, Jacob [UNIFESP]; Sociedade Brasileira de Dermatologia; Complexo Hospitalar Heliópolis Serviço de Reumatologia; Universidade Federal de São Paulo (UNIFESP); Complexo Hospitalar Heliópolis Serviço de Dermatologia
    Bullous systemic lupus erythematosus is recognized as a distinct entity related to autoimmunity to type VII collagen. In some cases, the flare of bullous disease coincides with the exacerbation of systemic lupus erythematosus, and especially lupus nephritis. Two cases of young female patients with vesiculobullous eruption on sun-exposed and non-exposed areas associated to lupus nephritis are described. Diagnosis was proved by characteristic histopathology and direct immunofluorescence. Corticosteroids and dapsone therapy may be effective.