Base de dados : LILACS
Pesquisa : C16.320.850 [Categoria DeCS]
Referências encontradas : 48 [refinar]
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Id: biblio-887069
Autor: Sánchez, María Encarnación Gómez; Martínez, Maria Luisa Martínez; Mena, Jose Luis Agudo; Martín, Luis Iñiguez De Onzoño.
Título: Osteoma cutis: rare painful tumor in atypical location
Fonte: An. bras. dermatol;92(5,supl.1):113-114, 2017. graf.
Idioma: en.
Resumo: Abstract Osteoma cutis or cutaneous ossification is a rare entity characterized by the formation of bone in the skin. We present an isolated primary osteoma cutis located on the palm, an atypical location.
Descritores: Dermatopatias Genéticas/patologia
Doenças Ósseas Metabólicas/patologia
Ossificação Heterotópica/patologia
Dermatoses da Mão/patologia
-Dor/etiologia
Biópsia
Doenças Raras
Limites: Seres Humanos
Masculino
Adulto
Tipo de Publ: Relatos de Casos
Responsável: BR1.1 - BIREME


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Id: biblio-887057
Autor: Heras, Marta Olivé; Muñoz, Noelia Pérez; Sancho, Maribel Iglesias; Millet, Pablo Umbert.
Título: Eosinophilic annular erythema in adults: report of two cases and review of the literature
Fonte: An. bras. dermatol;92(5,supl.1):65-68, 2017. graf.
Idioma: en.
Resumo: Abstract We herein report two cases of eosinophilic annular erythema in adults, which is rare. In both patients, lesions developed rapidly in few days and were located mainly on the trunk, buttocks, and extremities. Diagnosis was histopathological, with typical features including acute dermal inflammatory infiltrate with abundant eosinophils. One of the patients recurred after treatment on three occasions and finally cured spontaneously. The second patient recurred once and was then successfully treated with topical clobetasol. Clinical and histopathological features of eosinophilic annular erythema in adults have rarely been reported. A review of the literature and discussion of relationship with Wells syndrome are also included.
Descritores: Dermatopatias Genéticas/patologia
Celulite (Flegmão)/patologia
Eosinofilia/patologia
Eritema/patologia
-Biópsia
Doenças Raras
Eosinófilos/patologia
Limites: Seres Humanos
Masculino
Idoso
Tipo de Publ: Relatos de Casos
Revisão
Responsável: BR1.1 - BIREME


  3 / 48 LILACS  
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Id: biblio-887027
Autor: Lima, Caren dos Santos; Lemes, Luciana Rodino; Melo, Daniel Fernandes.
Título: Yellow dots in trichoscopy: relevance, clinical significance and peculiarities
Fonte: An. bras. dermatol;92(5):724-726, Sept.-Oct. 2017. graf.
Idioma: en.
Resumo: Abstract: Yellow dots are follicular ostium filled with keratin and/or sebum. Initially, they were exclusively associated with alopecia areata. Currently they have also been described in androgenetic alopecia, chronic cutaneous (discoid) lupus erythematosus, and dissecting cellulitis. Due to the growing importance of trichoscopy and its findings in the evaluation of the scalp, this article describes the main diseases in which yellow dots are a common trichoscopic finding, highlighting its characteristics in each dermatosis.
Descritores: Dermatoses do Couro Cabeludo/diagnóstico por imagem
Dermatopatias Genéticas/diagnóstico por imagem
Celulite (Flegmão)/diagnóstico por imagem
Alopecia em Áreas/diagnóstico por imagem
-Dermatoses do Couro Cabeludo/complicações
Dermatopatias Genéticas/complicações
Celulite (Flegmão)/complicações
Dermoscopia
Diagnóstico Diferencial
Alopecia em Áreas/etiologia
Limites: Seres Humanos
Responsável: BR1.1 - BIREME


  4 / 48 LILACS  
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Id: biblio-886966
Autor: Abuawad, Yasmin Gama; Uchiyama, Juliana; Kakizaki, Priscila; Valente, Neusa Yuriko Sakai.
Título: Primary cutaneous amyloidosis of the auricular concha - case report
Fonte: An. bras. dermatol;92(3):433-434, May-June 2017. graf.
Idioma: en.
Descritores: Dermatopatias/patologia
Dermatopatias Genéticas/patologia
Amiloidose Familiar/patologia
Pavilhão Auricular/patologia
Limites: Seres Humanos
Feminino
Adulto
Meia-Idade
Idoso
Tipo de Publ: Carta
Responsável: BR1.1 - BIREME


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Id: biblio-887101
Autor: Belli, Asli Akin; Kara, Asude; Dere, Yelda; Yilmaz, Nevin.
Título: Association of amyloidosis cutis dyschromica and familial Mediterranean fever
Fonte: An. bras. dermatol;92(5,supl.1):21-23, 2017. graf.
Idioma: en.
Resumo: Abstract: Amyloidosis cutis dyschromica is a rare type of primary cutaneous amyloidosis characterized by reticulate hyper-pigmentation with discrete hypopigmented macules. Up to date, about 50 cases of amyloidosis cutis dyschromica have been reported and the majority are familial cases of Asian ethnicity. Various diseases, particularly autoimmune diseases such as systemic sclerosis and systemic lupus erythematosus, have been associated with amyloidosis cutis dyschromica. Herein, we report a case of amyloidosis cutis dyschromica accompanying familial Mediterranean fever with a delayed diagnosis of 40 years. To the best of our knowledge, this is the first report of the association of amyloidosis cutis dyschromica and familial mediterranean fever.
Descritores: Febre Familiar do Mediterrâneo/complicações
Dermatopatias Genéticas/complicações
Dermatopatias Genéticas/patologia
Amiloidose Familiar/complicações
Amiloidose Familiar/patologia
-Biópsia
Hiperpigmentação/patologia
Derme/patologia
Limites: Seres Humanos
Feminino
Meia-Idade
Tipo de Publ: Relatos de Casos
Responsável: BR1.1 - BIREME


  6 / 48 LILACS  
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Id: biblio-887115
Autor: Cuevas-Gonzalez, Juan Carlos; Vega-Memíje, María Elisa; Borges-Yáñez, Socorro Aída; Rodríguez-Lobato, Erika.
Título: Risk factors associated with actinic prurigo: a case control study
Fonte: An. bras. dermatol;92(6):774-778, Nov.-Dec. 2017. tab.
Idioma: en.
Resumo: Abstract: Background: Actinic prurigo (AP) is an idiopathic photodermatosis. Although its initial manifestations can appear in 6 to 8-year-old children, cases are diagnosed later, between the second and fourth decades of life, when the injuries are exacerbated. Objective: To identify risk factors associated with clinical manifestations of AP such as skin and mucosal lesions. Methods: Thirty patients with AP and 60 controls were included in the study, the dependent variable was the presence of skin or labial mucosal lesions, the independent variables were age, sex, solar exposure, living with pets or farm animals, exposure to wood smoke, smoking habit, years smoking, and hours spent per day and per week in contact with people who smoke. Results: Of the 30 diagnosed AP patients, 66.7% were female. Patients age ranged from 7 to 71 years and the mean age was 35.77 ± 14.55 years. We found significant differences with the age and cohabitation with farm animals. Those who lived with farm animals presented 14.31 times higher probability of developing AP (95% CI 3-78.06). Study limitations: This is a case-control study; therefore, a causal relationship cannot be proven, and these results cannot be generalized to every population. Conclusions: The identification of factors related to the development of AP increases our knowledge of its physiopathology. Moreover, identifying antigens that possibly trigger the allergic reaction will have preventive and therapeutic applications in populations at risk of AP.
Descritores: Transtornos de Fotossensibilidade/etiologia
Dermatopatias Genéticas/etiologia
Exposição Ambiental/efeitos adversos
-Transtornos de Fotossensibilidade/fisiopatologia
Dermatopatias Genéticas/fisiopatologia
Luz Solar/efeitos adversos
Fatores de Tempo
Estudos de Casos e Controles
Modelos Logísticos
Fatores de Risco
Fatores Etários
Estatísticas não Paramétricas
Hipersensibilidade/etiologia
Hipersensibilidade/fisiopatologia
Animais Domésticos
Limites: Seres Humanos
Animais
Masculino
Feminino
Criança
Adolescente
Adulto
Meia-Idade
Idoso
Adulto Jovem
Responsável: BR1.1 - BIREME


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Id: biblio-827767
Autor: MA, Han; Su, Xiangyang; Zhu, Guoxing; Yin, Songchao; Lu, Chun; Lai, Wei.
Título: Primary localized cutaneous amyloidosis with lichen and poikiloderma-like lesions and an excellent response to systemic acitretin
Fonte: An. bras. dermatol;91(5):661-663, Sept.-Oct. 2016. graf.
Idioma: en.
Resumo: Abstract: Primary localized cutaneous amyloidosis is a skin-limited amyloidosis that does not involve internal organs. It is clinically subclassified into 3 general categories and some rare variants. However, there is considerable overlap within the classification. Though there are a variety of therapeutic measures, the treatment is often unsatisfactory, particularly when the disease is severe and extensive. We describe a rare case of primary localized cutaneous amyloidosis with lichen and poikiloderma-like lesions that showed an excellent response to systemic acitretin.
Descritores: Dermatopatias Genéticas/tratamento farmacológico
Acitretina/uso terapêutico
Amiloidose Familiar/tratamento farmacológico
Ceratolíticos/uso terapêutico
-Dermatopatias Genéticas/complicações
Dermatopatias Genéticas/diagnóstico
Resultado do Tratamento
Erupções Liquenoides/complicações
Erupções Liquenoides/tratamento farmacológico
Amiloidose Familiar/complicações
Amiloidose Familiar/diagnóstico
Limites: Seres Humanos
Feminino
Adulto Jovem
Tipo de Publ: Relatos de Casos
Responsável: BR1.1 - BIREME


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Cestari, Silmara da Costa Pereira
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Id: biblio-837943
Autor: Maciel, Marina Gagheggi; Enokihara, Milvia Maria Simões e Silva; Seize, Maria Bandeira de Melo Paiva; Marcassi, Aline Pantano; Piazza, Christiane Affonso De Donato; Cestari, Silmara da Costa Pereira.
Título: Elastoma: clinical and histopathological aspects of a rare disease
Fonte: An. bras. dermatol;91(5,supl.1):39-41, Sept.-Oct. 2016. graf.
Idioma: en.
Resumo: Abstract Elastoma is a connective tissue nevus characterized by changes in elastic fibers. It can be congenital or acquired, and is usually diagnosed before puberty. Associated with osteopoikilosis, it is known as Buschke-Ollendorff syndrome. Histopathology with specific staining for elastic fibers is critical for a diagnostic conclusion. This report describes the case of a 7-year-old male patient with lesions diagnosed as elastoma, with absence of bone changes in the radiological imaging. This study aims to report the clinical presentation and histological examination of such unusual disease.
Descritores: Tecido Elástico/patologia
Nevo/patologia
-Osteopecilose/patologia
Dermatopatias Genéticas/patologia
Biópsia
Derme/patologia
Doenças Raras/patologia
Diagnóstico Diferencial
Limites: Seres Humanos
Masculino
Criança
Tipo de Publ: Relatos de Casos
Responsável: BR1.1 - BIREME


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Id: lil-792433
Autor: Abarzúa, Alvaro; Giesen, Laura; Silva, Sergio; González, Sergio.
Título: Eosinophilic annular erythema in childhood - Case report
Fonte: An. bras. dermatol;91(4):503-505, July-Aug. 2016. graf.
Idioma: en.
Resumo: Abstract: Eosinophilic annular erythema is a rare, benign, recurrent disease, clinically characterized by persistent, annular, erythematous lesions, revealing histopathologically perivascular infiltrates with abundant eosinophils. This report describes an unusual case of eosinophilic annular erythema in a 3-year-old female, requiring sustained doses of hydroxychloroquine to be adequately controlled.
Descritores: Dermatopatias Genéticas/patologia
Dermatopatias Genéticas/sangue
Eosinofilia/patologia
Eritema/patologia
Eritema/sangue
-Pele/patologia
Biópsia
Eosinófilos/patologia
Limites: Seres Humanos
Feminino
Pré-Escolar
Tipo de Publ: Relatos de Casos
Responsável: BR1.1 - BIREME


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Id: biblio-837946
Autor: Marcarini, Renata; Araujo, Raquel Nardelli de; Nóbrega, Monisa Martins; Medeiros, Karina Bittencourt; Gripp, Alexandre Carlos; Maceira, Juan Manuel Piñeiro.
Título: Histiocytoid Sweet's syndrome presenting with annular erythematous plaques
Fonte: An. bras. dermatol;91(5,supl.1):154-156, Sept.-Oct. 2016. tab, graf.
Idioma: en.
Resumo: Abstract Histiocytoid Sweet's Syndrome is a rare inflammatory disease described in 2005 as a variant of the classical Sweet's Syndrome (SS). Histopathologically, the dermal inflammatory infiltrate is composed mainly of mononuclear cells that have a histiocytic appearance and represent immature myeloid cells. We describe a case of Histiocytoid Sweet's Syndrome in an 18-year-old man. Although this patient had clinical manifestations compatible with SS, the cutaneous lesions consisted of erythematous annular plaques, which are not typical for this entity and have not been described in histiocytic form so far. The histiocytic subtype was confirmed by histopathological analysis that showed positivity for myeloperoxidase in multiple cells with histiocytic appearance.
Descritores: Dermatopatias Genéticas/patologia
Síndrome de Sweet/patologia
Eritema/patologia
Histiócitos/patologia
-Pele/patologia
Biópsia
Neutrófilos/patologia
Limites: Seres Humanos
Masculino
Adolescente
Tipo de Publ: Relatos de Casos
Responsável: BR1.1 - BIREME



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