Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
J Med Vasc ; 44(4): 291-294, 2019 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-31213302

RESUMO

Inflammatory bowel diseases are associated with a state of hypercoagulability secondary to several mechanisms, protein S deficiency being one of these. It can be revealed by spontaneous skin necrosis in children. This condition is rare in adults with Crohn's disease. We are reporting a case of a 35-year-old woman with active Crohn's disease who presented a protein S deficiency responsible for an extensive spontaneous skin necrosis. The evolution was favourable after vascular filling, curative anticoagulation, antibiotic therapy, as well as a high-dose of corticosteroid therapy. We are reporting this case in order to emphasize the importance of considering skin necrosis as a possible cutaneous manifestation of inflammatory bowel diseases.


Assuntos
Doença de Crohn/complicações , Deficiência de Proteína S/complicações , Dermatopatias/etiologia , Pele/patologia , Corticosteroides/administração & dosagem , Adulto , Antibacterianos/administração & dosagem , Anticoagulantes/administração & dosagem , Doença de Crohn/diagnóstico , Doença de Crohn/tratamento farmacológico , Feminino , Humanos , Necrose , Deficiência de Proteína S/diagnóstico , Deficiência de Proteína S/tratamento farmacológico , Pele/efeitos dos fármacos , Dermatopatias/tratamento farmacológico , Dermatopatias/patologia , Resultado do Tratamento
2.
Epidemiol Infect ; 144(16): 3365-3375, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27535719

RESUMO

Hepatitis B virus (HBV) vaccination has been part of the Expanded Programme of Immunization (EPI) in Tunisia since 1995. The aim of this study was to evaluate, for the first time, the impact of mass vaccination in Tunisia 17 years after this programme was implemented, and in parallel, assess the long-term persistence of anti-HBs antibody in the vaccinated Tunisian population. A total of 1422 students were recruited (703 vaccinated, 719 non-vaccinated). HBV seromarkers were checked. None of the students from either group had positive HBsAg. The overall prevalence of anti-HBc was 0·8%. A Significantly higher prevalence of anti-HBc was noted in unvaccinated students than in vaccinated (1·4% vs. 0·3%, P = 0·02). The overall seroprotection rate (anti-HBs titre ⩾10 mIU/ml) was 68·9% in vaccinated subjects. Seroprotection rates and geometric mean titres decreased significantly with increasing age, reflecting waning anti-HBs titre over time. No significant difference was detected between seroprotection rates and gender or students' area of origin. Incomplete vaccination was the only factor associated with an anti-HBs titre <10 mIU/ml. This study demonstrates the excellent efficacy of the HBV vaccination programme in Tunisia 17 years after its launch. However, a significant decline of anti-HBs seroprotection has been observed in ⩾15-year-old adolescents which places them at risk of infection. Additional studies are needed in hyperendemic regions in Tunisia.

3.
J Mal Vasc ; 39(3): 203-6, 2014 May.
Artigo em Francês | MEDLINE | ID: mdl-24412009

RESUMO

Thrombotic events occurring in the course of celiac disease are frequently reported in the literature. The localization is often unusual, mainly affecting the hepatic veins. To our knowledge, this is the first report of intracardiac thrombosis occurring in a patient with celiac disease. A 32-year-old patient with celiac disease adhered poorly to his gluten-free diet. He suffered an ischemic stroke revealing an intracardiac thrombus, which, on radiological imaging, simulated a multiple myxoma. Histological examination of the resected tumor enabled the correct diagnosis. Biological findings revealed severe protein C and S deficiency. The patient improved with anticoagulant therapy and gluten-free diet.


Assuntos
Doença Celíaca/complicações , Cardiopatias/etiologia , Neoplasias Cardíacas/complicações , Mixoma/complicações , Neoplasias Primárias Múltiplas/complicações , Deficiência de Proteína C/complicações , Deficiência de Proteína S/complicações , Trombose/etiologia , Adulto , Anticoagulantes/uso terapêutico , Doença Celíaca/dietoterapia , Diabetes Mellitus Tipo 1/complicações , Dieta Livre de Glúten , Cardiopatias/diagnóstico , Cardiopatias/tratamento farmacológico , Neoplasias Cardíacas/diagnóstico , Hemangioma Cavernoso/complicações , Humanos , Achados Incidentais , Neoplasias Hepáticas/complicações , Imagem Cinética por Ressonância Magnética , Masculino , Mixoma/diagnóstico , Neoplasias Primárias Múltiplas/diagnóstico , Deficiência de Proteína C/diagnóstico , Deficiência de Proteína C/tratamento farmacológico , Deficiência de Proteína S/diagnóstico , Deficiência de Proteína S/tratamento farmacológico , Infarto do Baço/etiologia , Trombose/diagnóstico , Trombose/tratamento farmacológico , Trombose Venosa/etiologia
4.
Rev Med Interne ; 32(1): e1-3, 2011 Jan.
Artigo em Francês | MEDLINE | ID: mdl-21035926

RESUMO

Intestinal pseudo-obstruction (IPO) is an uncommon and severe complication of systemic lupus erythematosus (SLE). We report a 24-year-old female with a 2 year SLE duration who presented with abdominal pain, vomiting, constipation and abdominal distention. Plain abdominal radiograph showed multiple air-fluid levels of the small bowel. Computed tomographic scan of the abdomen revealed dilated small bowel loops without mechanical obstruction. Urinary tract involvement was also demonstrated. IPO was diagnosed and the patient responded well to immunosuppressive treatment. IPO is a recently recognized manifestation of SLE that may be the presenting manifestation of the systemic disease or occur more commonly during disease course. Early recognition of IPO is necessary to institute appropriate medical treatment and to avoid inappropriate surgical intervention.


Assuntos
Pseudo-Obstrução Intestinal/complicações , Pseudo-Obstrução Intestinal/diagnóstico , Intestino Delgado , Lúpus Eritematoso Sistêmico/complicações , Lúpus Eritematoso Sistêmico/tratamento farmacológico , Dor Abdominal/etiologia , Adulto , Doença Crônica , Constipação Intestinal/etiologia , Diagnóstico Precoce , Feminino , Humanos , Imunossupressores/uso terapêutico , Pseudo-Obstrução Intestinal/etiologia , Resultado do Tratamento , Vômito/etiologia
5.
J Mal Vasc ; 35(1): 4-11, 2010 Feb.
Artigo em Francês | MEDLINE | ID: mdl-19879079

RESUMO

BACKGROUND: Takayasu's arteritis is a rare inflammatory disease and few data are available in Tunisia. The aim of this study is to evaluate clinical and radiological features of the disease in the centre of Tunisia. METHODS: We retrospectively studied medical records of patients treated in departments of internal medicine or cardiology from three university hospitals in Sousse and Monastir over the period 1985-2005. The criteria for inclusion were those proposed by the American College of Rheumatology. RESULTS: Twenty-seven patients were identified. The mean age at presentation was 33.2 years (range 16-68 years) and 88.9% were female. The mean delay from the onset of the symptoms to the time of diagnosis was 4.2 years. Intermittent claudication was the most common presentation (81.5%) and hypertension was noted in 40.7% of cases. Arterial localization most frequently involved was subclavian artery. The aorta was involved in 52.3% and renal arteries in 36.3% of cases. Stenosis or occlusions was constant but aneurysms were noted in 7.4%. Functional difficulty was the main complaint in the follow-up, death related to Takayasu's disease was noted in 3.7%. The mean follow-up time was 75.8 months (6.3 years). CONCLUSION: There is no epidemiologic particularity of Takayasu's disease in Tunisia, however involvement of the subclavian artery was more frequent than the aortic localization.


Assuntos
Arterite de Takayasu/epidemiologia , Adolescente , Corticosteroides/uso terapêutico , Adulto , Idoso , Angiografia , Angioplastia , Terapia Combinada , Feminino , Humanos , Claudicação Intermitente/etiologia , Masculino , Pessoa de Meia-Idade , Gravidez , Complicações Cardiovasculares na Gravidez/diagnóstico , Estudos Retrospectivos , Arterite de Takayasu/diagnóstico , Arterite de Takayasu/diagnóstico por imagem , Arterite de Takayasu/tratamento farmacológico , Arterite de Takayasu/cirurgia , Tunísia/epidemiologia , Adulto Jovem
8.
Med Mal Infect ; 37(12): 792-5, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17870271

RESUMO

BACKGROUND: Infections are common in patients with systemic lupus erythematosus (SLE) throughout the course of their disease and remain a source of mortality. The aim of this study was to determine the prevalence of infections, to describe their nature, and analyze their risk factors in adults with SLE. PATIENTS AND METHODS: We performed a descriptive study, at the Farhat-Hached Hospital in Sousse, and retrospectively analyzed the charts of 75 patients with SLE seen between 1990 and 2004. The group of patients with documented infections was compared to a control group. A logistic regression analysis was performed to determine risk factors associated with infection. RESULTS: Our study included 64 women and 11 men (median age of 31.4 years). Forty-three patients (57.5%) had 82 infectious episodes: 23 patients had at least two infectious episodes. Most infections were community acquired, and 80% were severe. The most common infections involved the urinary tract (28%), the skin and soft tissue (26.8%), and the respiratory tract (18.3%). Documented pathogens were: 45 common bacteria, 11 Candida albicans and four Mycobacterium tuberculosis. Localized herpes zoster was noted in three cases. Factors associated with infection, found in univariate analysis, were renal involvement, serum albumin lower than 25 g/l, and corticosteroids treatment. Only corticosteroids therapy remained statistically significant after multivariate analysis.


Assuntos
Infecções/epidemiologia , Lúpus Eritematoso Sistêmico/complicações , Adolescente , Adulto , Idoso , Infecções Bacterianas/epidemiologia , Infecções Comunitárias Adquiridas/epidemiologia , Feminino , Humanos , Lúpus Eritematoso Sistêmico/microbiologia , Masculino , Pessoa de Meia-Idade , Prevalência , Estudos Retrospectivos
9.
Ann N Y Acad Sci ; 1078: 176-9, 2006 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-17114704

RESUMO

Although Mediterranean spotted or "boutonneuse" fever (MSF) has been documented in central Tunisia, other spotted fever group rickettsioses (SFGR) and typhus group rickettsioses (TGR) have received little attention in our region. We sought to determine the role of rickettsioses, Q fever, ehrlichioses, and bartonelloses among patients with acute fever. The results of this study of 47 persons with acute fever of undetermined origin are reported in this paper. We concluded that SFGR, murine typhus, and acute Q fever are common causes of acute isolate fever in summer in central Tunisia and should be investigated systematically in patients with acute fever of unknown origin.


Assuntos
Febre/microbiologia , Infecções por Rickettsia/diagnóstico , Adolescente , Adulto , Idoso , Anticorpos Antibacterianos/sangue , Feminino , Hospitais Universitários , Humanos , Masculino , Pessoa de Meia-Idade , Testes Sorológicos , Tunísia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...