Behcet Syndrome
Mostrando 1-12 de 70 artigos, teses e dissertações.
-
1. Giant Left Anterior Descending Coronary Artery Aneurysm in a Patient with Behçet’s Disease
ABSTRACT Coronary artery involvement is quite rare in the course of Behçet’s disease. Complications secondary to coronary artery aneurysms, including rupture, dissection, and myocardial ischemia, may be fatal. In young patients without cardiovascular risk factors, systemic inflammatory vasculitis syndromes should be investigated in case of acute coronary
Brazilian Journal of Cardiovascular Surgery. Publicado em: 2022
-
2. Case for diagnosis. Ulcerated lesions: a diagnostic challenge in Behçet's syndrome
Abstract This study reports the clinical case of a 42-year-old patient with ulcerated lesions who was followed up by general practitioners with the diagnosis of recurrent cellulitis. However, when referred to the Dermatology division a diagnosis of Behçet's syndrome was established based on clinical criteria. Although there are defined clinical criteria for
An. Bras. Dermatol.. Publicado em: 2021-08
-
3. Coronary Involvement in Behçet's Disease: what are its Risks and Prognosis? (Rare Cases and Literature Review)
Abstract Objective: In our clinic, we aimed to investigate the effect of preoperative risk factors and postoperative complications on reoperation and mortality in cases with Behçet's disease which presents very rare coronary artery involvement. Methods: Thirteen patients with Behçet's Disease who had undergone coronary artery bypass grafting in our cen
Braz. J. Cardiovasc. Surg.. Publicado em: 01/07/2019
-
4. Syndrome In Question
The authors present a male 40-year-old patient with established diagnosis of Behçet's disease which had evolved to recurrent bilateral auricular polychondritis crises. MAGIC syndrome (mouth and genital ulcers with inflamed cartilage) is rare and groups together patients with this clinical picture without necessarily fulfilling the clinical criteria for Beh�
An. Bras. Dermatol.. Publicado em: 2014-01
-
5. Doença de Behçet : dados demográficos e manifestações clínicas em 87 pacientes acompanhados no ambulatório de vasculites do Hospital das Clínicas da Cidade de Campinas / Behçet s disease : demographic and clinical features in 87 patients treated at UNICAMP
Objetivo: Descrever os dados demográficos e as manifestações clinicas de pacientes com diagnostico de Doença de Behcet acompanhados no ambulatório de vasculites do Hospital das Clinicas da cidade de Campinas, São Paulo, Brasil. Métodos: O estudo foi realizado através da revisão dos prontuários de todos os pacientes com diagnostico de Doença de Beh
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 10/06/2011
-
6. Expression of toll-like receptor 2 and neutrophil chemotaxis in Behçet´s disease / Expressão de receptores toll-like 2 e função quimiotáxica de neutrófilos na doença de Behçet
Expressions of toll-like receptor (TLR) 2, TLR4, CD14, CD114 and CD116 were assessed on polymorphonuclear (PMN) neutrophils and monocytes of patients with Behçets disease (BD). PMN chemotactic responses under different stimulations were also measured. The objective was to determine if BD PMN chemotaxis may be overstimulated by lipoteichoic acid (LTA) from g
Publicado em: 2009
-
7. Genital ulcers in women: clinical, microbiologic and histopathologic characteristics
Female genital ulcer is a disease that affects a large number of women, and its etiologic diagnosis can be difficult. The disease may increase the risk of acquiring HIV. Genital ulcer may be present in sexually transmitted diseases (STD) - syphilis, chancroid, genital herpes, donovanosis, lymphogranuloma venereum and other non-STD disorders (NSTD) - Behçet'
Brazilian Journal of Infectious Diseases. Publicado em: 2007-04
-
8. A family study of Behcet's syndrome.
The first-degree family members of patients with Behcet's syndrome were investigated to determine (1) whether there was a familial aggregation of Behcet's syndrome or of its component features, (2) whether there was an increased incidence of sacro-iliitis in these families, and (3) whether a link exists between Behcet's syndrome and spondarthritides in first
-
9. Polymorphonuclear function in Behçet's syndrome.
Three aspects of polymorphonuclear leucocyte (PMN) function were studied in 19 patients with Behçet's syndrome (BS). By 2 different techniques directed motility was found to be increased. This increase was largely due to the subgroup of patients with ocular involvement. Counts of absolute numbers of cells migrating highlighted this finding. No difference wa
-
10. Close association of HLA-B51 and B52 in Israeli patients with Behçet's syndrome.
Epidemiological data, family history, clinical data, and HLA typing were studied in three groups of patients with Behçet's syndrome: six Israeli Ashkenazi Jews, 29 non-Ashkenazi Jews, and three Israeli Arabs. HLA-B51 and B52 were present in 24/38 (63%) and 8/38 (21%), respectively, of the patients compared with 13/151 (9%) of the control group for both case
-
11. Genetic analysis of families of patients with Behçet's syndrome: data incompatible with autosomal recessive inheritance.
Data on families with Behçet's syndrome were analysed to test a hypothesis of autosomal recessive inheritance. Fifteen families from the UK and nine from Turkey were included. There were 27 individuals with Behçet's syndrome according to the Japanese criteria and 119 unaffected individuals. There were no affected parents in the families. The 'goodness of f
-
12. Synovial histopathology of behçet's syndrome.
Synovial tissue obtained from 7 patients with Behçet's syndrome and 7 patients with early rheumatoid arthritis could not be distinguished under ordinary light microscopy when examined blind. A wide spectrum of features was seen in both diseases, and it is suggested that these may reflect severity and duration as much as the nature of the arthritis. Electron