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Search Results: 1 - 10 of 62408 matches for " Everton Carlos Siviero do; "
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Primeiro atendimento em queimaduras: a abordagem do dermatologista
Vale, Everton Carlos Siviero do;
Anais Brasileiros de Dermatologia , 2005, DOI: 10.1590/S0365-05962005000100003
Abstract: despite continued progress obtained recently in treating the massively burned, mortality and morbidity rates remain quite high. implementation of preventive strategies has still not managed to significantly alter the dramatic epidemiological picture of burns patients. survivors of severe burns still carry a heavy load of physical and psychosocial sequelae, which engenders a considerable share of suffering to overcome. there is little doubt that the final prognosis of a burn essentially depends on prompt and adequate inicial management. this is why it is important for all physicians, including dermatologists, to be able to guide first aid for and manage initially a burns victim. the aim of this article is to review the pathophysiology of burns and the principles according to which a burns victim is assessed. in addition, it is discussed a single and objective way of carrying out the emergency medical care until the victim be moved to a burns unit, if needed.
Elastólise pós-inflamatória e cutis laxa (doen?a de James Marshall): estudo de casos
Aguilar, Claudemir Roberto;Gontijo, Bernardo;Vale, Everton Carlos Siviero do;
Anais Brasileiros de Dermatologia , 2007, DOI: 10.1590/S0365-05962007000400004
Abstract: background: although rare diseases, one third of all cases of post-inflammatory elastolysis and cutis laxa published in the international literature are from the state of minas gerais, in brazil. reports with long term follow-up of these patients are also scarce. objectives: to report nine cases observed from 1981 to 2004 and compare the findings with 20 cases described in the literature. methods: epidemiological, clinical, pathological and therapeutical variables were assessed. results: the onset of the disease is usually up to the age of four years (93%), and it is more common in african americans (8:1), females (4:1) and in tropical climate (9:1). other features include alpha-1-antitrypsin deficiency (7%), aortitis (7%), related skin conditions (62%), premature facial ageing (97%) and stable atrophic phase during childhood after months or years with inflammatory lesions (97%). biopsies of recent lesions showed a more intense inflammatory infiltrate and less elastolysis than those obtained from older lesions. reconstructive surgery yielded good results during atrophic phase and 0.05% topical tretinoin was ineffective. conclusions: in 62% of patients the acute phase of post-inflammatory elastolysis and cutis laxa is associated with different elastolysis-promoting inflammatoy dermatoses. the correct management of these conditions may reduce severity of atrophic lesions, which can also be treated by reconstructive surgery. alpha-1-antitrypsin deficiency should be investigated.
Síndrome de Muckle-Wells em quatro membros de uma família
Pereira, Ana Francisca Junqueira Ribeiro;Pereira, Luciana Baptista;Vale, Everton Carlos Siviero do;Tanure, Leandro Augusto;
Anais Brasileiros de Dermatologia , 2010, DOI: 10.1590/S0365-05962010000600022
Abstract: muckle-wells syndrome is a rare autosomal dominant disease that belongs to a group of hereditary febrile syndromes. it is characterized by recurrent and self-limited episodes of fever, urticaria, arthralgia, myalgia and conjunctivitis since childhood, which are related to exposure to cold temperatures. lately, progressive sensorineural hearing loss occurs. amyloidosis is the main complication and can be found in about 25% of the cases. it has been demonstrated that there is an association with mutations in the nlrp3 gene, which codifies cryopyrin, a protein responsible for regulating the production of proinflammatory cytokines, such as interleukin-1beta. the authors report four cases of the disease within a family.
Você conhece esta síndrome?
Ottoni, Fernanda Assis;Froes, Giselle Carvalho;Pimenta, Mariana Rodrigues;Vale, Everton Carlos Siviero do;
Anais Brasileiros de Dermatologia , 2006, DOI: 10.1590/S0365-05962006000500013
Abstract: a case of fanconi anemia is reported, with typical cutaneous manifestations of diffuse hyperpigmentation and café-au-lait spots. he also presented thumb hypoplasia, short stature, cataract, hypoacusis, pelvic kidneys and chromosome breakage. presently 30-years-old, the patient is stable, with leukopenia and macrocytosis without clinical symptoms, in contrast to usual prognosis of this syndrome, which involves early death due to complications of bone marrow aplasia, leukemia and solid tumors.
Caso para diagnóstico
Barbosa, Ana Luiza Baeta Pereira;Domingos, Eduardo Aurélio Gomes;Vale, Everton Carlos Siviero do;
Anais Brasileiros de Dermatologia , 2006, DOI: 10.1590/S0365-05962006000200013
Abstract: a case of mucinous nevus is reported in a male teenager who presented assymptomatic brown papules confluent in linear plaques in the left hip since the age of 14 years old. further on mucin deposition in superficial dermis, the histopathology showed reduction of elastic fibers in the papillary dermis, hiperkeratosis, acanthosis and papillomatosis.
Case for diagnosis
Cherobin, Ana Carolina Figueiredo Pereira;Oliveira, Felipe Osta de;Baeta, Isabela Guimar?es Ribeiro;Vale, Everton Carlos Siviero do;
Anais Brasileiros de Dermatologia , 2012, DOI: 10.1590/S0365-05962012000100025
Abstract: dyschromicum erythema perstans, or ashy dermatosis, is a rare chronic acquired skin disease characterized by gray hyperpigmented patches with erythematous borders. its etiology is unknown and there is no specific treatment for the condition. we report a case of ashy dermatosis in a 41-year-old patient with extensive lesions on the trunk and limbs.
Elastose perfurante serpiginosa em portadora da síndrome de Down
Pereira, Ana Carolina Figueiredo;Baeta, Isabela Guimar?es Ribeiro;Costa Júnior, Sérgio Rodrigues da;Gontijo Júnior, Oswaldo Macedo;Vale, Everton Carlos Siviero do;
Anais Brasileiros de Dermatologia , 2010, DOI: 10.1590/S0365-05962010000500015
Abstract: elastosis perforans serpiginosa is a rare, primary perforating dermatosis, frequently associated with certain genetic diseases and characterized by the transepidermal extrusion of elastic fibers. the present case report describes this dermatosis in a 19-year old female patient with down's syndrome, who presented with asymptomatic erythematous, keratotic papules in an arciform pattern, located on her right forearm and knee, which had been present for five years. following histopathological confirmation, treatment with cryotherapy was initiated, resulting in partial remission of the lesions.
A consolida o dos Anais no cenário das revistas médicas
Gontijo Bernardo,Marques Sílvio Alencar,Vale Everton Siviero do
Anais Brasileiros de Dermatologia , 2006,
Abstract:
Você conhece esta síndrome?
Sousa, Júnia Bicalho de;Carvalho, Sílvia Pimenta de;Pereira, Luciana Baptista;Vale, Everton Siviero do;
Anais Brasileiros de Dermatologia , 2006, DOI: 10.1590/S0365-05962006000100012
Abstract: congenital generalized lipodystrophy (berardinelli-seip syndrome) is a recessive autossomic disease characterized by absence of subcutaneous tissue. the fat tissue absence leads to metabolic dysfunction of lipids and carbohydrates, peripheral insulin resistance and increased seric levels of triglycerides and also a higher metabolic rate. other findings are acanthosis nigricans, acromegaly, hepatomegaly and muscular, bony, cardiovascular and neurological abnormalities. a case of a patient with this syndrome is reported, whose diagnosis was made in a dermatology ambulatory.
Você conhece esta síndrome?
Sousa Júnia Bicalho de,Carvalho Sílvia Pimenta de,Pereira Luciana Baptista,Vale Everton Siviero do
Anais Brasileiros de Dermatologia , 2006,
Abstract: A lipodistrofia generalizada congênita (síndrome de Berardinelli-Seip), doen a autoss mica recessiva, caracteriza-se por escassez do tecido subcutaneo. A falta de tecido adiposo propicia disfun o metabólica dos lípides e carboidratos, resistência periférica à insulina, hipertrigliceridemia e hipermetabolismo. Outros achados s o acantose nigricante, acromegalia, hepatomegalia e altera es musculares, ósseas, cardiovasculares e neurológicas. Relata-se o caso de paciente com essa síndrome, cujo diagnóstico foi realizado em um servi o de dermatologia.
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