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1.
Rev Esp Cardiol ; 54(7): 868-79, 2001 Jul.
Artigo em Espanhol | MEDLINE | ID: mdl-11446963

RESUMO

INTRODUCTION: Use of the left internal mammary artery to bypass the left anterior descending coronary artery reduces cardiac events and increases survival. However, there is some controversy as to the benefits of using both mammary arteries. OBJECTIVES: To assess the long-term outcome of the use of both mammary arteries in comparison with the use of only one. PATIENTS AND METHOD: A retrospective cohort study with a mean follow-up of 9.0 +/- 4.2 years was performed including 108 patients consecutively revascularized using both mammary arteries (II) and 108 patients randomly chosen in whom one mammary artery (I) was used for this purpose. RESULTS: Both groups were similar. There were no differences between the groups in operative morbidity or mortality. The survival at 10 years was similar (II: 84.61 +/- 4%; I: 85.18 +/- 3.8%), whereas recurrence of angina (II: 29.63 +/- 5.3%; I: 47.55 +/- 5.6%) (p = 0.012), the requirement for percutaneous angioplasty (II: 3.98 +/- 2%; I: 12.99 +/- 4.1%) (p = 0.009) and cardiologic events (II: 33.48 +/- 5.5%; I: 48.48 +/- 5.5%)(p = 0.022) were all lower in the group in which both mammary arteries were used. In the multivariate analysis, the use of both mammary arteries was an independent protective factor against angina recurrence (RR = 0.55), angioplasty (RR = 0.18) and cardiologic event (RR = 0.60). CONCLUSIONS: The use of both mammary arteries for revascularization does not increase operative morbidity. Since this procedure acts as an independent factor against angina recurrence, angioplasty and cardiologic event


Assuntos
Anastomose de Artéria Torácica Interna-Coronária/métodos , Feminino , Seguimentos , Humanos , Anastomose de Artéria Torácica Interna-Coronária/mortalidade , Masculino , Pessoa de Meia-Idade , Recidiva , Estudos Retrospectivos , Fatores de Tempo
3.
Minerva Stomatol ; 49(11-12): 521-5, 2000.
Artigo em Italiano | MEDLINE | ID: mdl-11345681

RESUMO

BACKGROUND: To evaluate the primary or secondary involvement of the submandibular gland in floor of mouth squamous cell carcinoma. METHODS: An analytic-observational study of prospective type was carried out on 31 patients operated for floor of mouth carcinoma, between June 1993 and January 1996, in a reference hospital for a population of 1,100,000 inhabitants. The investigated variables were: age, sex, tumor localization, clinical TNM, type of cervical surgery, evolution, number of positive cervical metastasis, state of the submandibular gland and presence of the periglandular metastasis. The follow-up period was about 48 to 76 months. The exact Fischer test was used for the statistical study. RESULTS: Histopathological examination identified cervical metastasis as 34.1% of the ipsilateral neck dissections. The average number of positive nodes was 3 (range: 1-9). Cervical periglandular metastases were found in 31.7% of neck dissections, but in no case was microscopic affectation of the submandibular gland found. The existence of intraglandular positive nodes was not found either. In our study, the sensibility and specificity of the clinical exploration of the submandibular region were high (84% and 88% respectively). The presence of cervical metastasis and the size of the tumor conditioned the appearance of recurrences. CONCLUSIONS: In accordance with our study, periglandular metastases in carcinoma of the floor of mouth, are frequent, but submandibular gland involvement is unusual.


Assuntos
Carcinoma de Células Escamosas/patologia , Neoplasias Bucais/patologia , Neoplasias da Glândula Submandibular/patologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Invasividade Neoplásica , Estudos Prospectivos
4.
Ann Otolaryngol Chir Cervicofac ; 116(5): 295-8, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10572594

RESUMO

Stafne bone cyst of the mandible is the only described destructive bone lesion that is highly localized, nonprogressive, but nonhealing. Such defects usually occur unilaterally, however, bilateral defects are occasionally reported. This paper reports 4 cases of Stafne's bone cyst, one of which showed bilateral presentation. Only four previous cases of bilateral Stafne bone cyst have been reported in the literature. The bibliography is reviewed with regard to the incidence, plausible etiologic factors and methods of diagnosis of such lesions.


Assuntos
Cistos Ósseos/diagnóstico por imagem , Doenças Mandibulares/diagnóstico por imagem , Adulto , Diagnóstico Diferencial , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Radiografia Panorâmica , Tomografia Computadorizada por Raios X
5.
Head Neck ; 21(7): 652-6, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10487953

RESUMO

BACKGROUND: Primary surgery is the appropriate treatment for most pleomorphic adenomas of the salivary glands. However, no reliable criteria have been established to predict tumors with aggressive features. METHODS: In 44 patients treated for salivary pleomorphic adenoma, clinicopathologic features and flow cytometric findings were recorded. S-phase fractions were classified as low (0%-1%), intermediate (1.1%-5%), and high (>5%). The relationship between clinicopathologic parameters and flow cytometric DNA analysis was assessed with the Pearson's correlation coefficient. RESULTS: The mean tumor size was 24.4 mm. Microscopically, myxoid structures predominated in 61.4% of cases. Only five specimens showed high S-phase fractions. All samples were DNA diploid (mean coefficient of variation 3.2%). S-phase fraction and tumor size correlated significantly (r = 0.73, P = 0.003). Two patients with recurrent tumors had high S-phase fractions both on the first resected specimens and at the time of the second operation. CONCLUSIONS: The S-phase fraction may be a valuable predictor of aggressive behavior in salivary pleomorphic adenomas. High S-phase fractions were associated with higher tumor size and a greater tendency to recur.


Assuntos
Adenoma Pleomorfo/patologia , Neoplasias das Glândulas Salivares/patologia , Adenoma Pleomorfo/diagnóstico , Adolescente , Adulto , Distribuição de Qui-Quadrado , DNA de Neoplasias/análise , Feminino , Citometria de Fluxo , Humanos , Masculino , Prognóstico , Estudos Prospectivos , Fase S , Neoplasias das Glândulas Salivares/diagnóstico , Sensibilidade e Especificidade
6.
Br J Cancer ; 79(7-8): 1302-3, 1999 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10098775

RESUMO

We screened the 185delAG and 5382insC (BRCA1) and the 6174delT (BRCA2) mutation in 298 Spanish women with breast cancer. Two women (one with Sephardic ancestors) presented the 185delAG mutation and the same haplotype reported in Ashkenazim with this mutation. This suggests a common origin of the 185delAG in both Sephardic and Ashkenazi populations.


Assuntos
Neoplasias da Mama/genética , Genes BRCA1/genética , Judeus , Proteínas de Neoplasias/genética , Fatores de Transcrição/genética , Adulto , Proteína BRCA2 , Neoplasias da Mama/etnologia , Feminino , Marcadores Genéticos , Haplótipos , Humanos , Repetições de Microssatélites/genética , Pessoa de Meia-Idade , Mutação , Espanha/etnologia
7.
Clin Genet ; 54(2): 142-7, 1998 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-9761393

RESUMO

The recent isolated gene BRCA2 is responsible for about 45% of familial breast cancer and the majority of male breast cancer families. In order to evaluate the role of inherited BRCA2 mutations in Spanish families, the complete coding sequence of the gene was screened by SSCP/sequencing in 16 high-risk breast/ovarian cancer families. Four mutations were found that cause a premature termination codon. Two of them have been reported elsewhere and one is a novel mutation. In addition we have found seven polymorphisms, two of which have not been previously described. One of the mutations, 936delAAAC was found in two of our high-risk families. Because this mutation is considered as recurrent, we have tried to estimate its frequency in our breast cancer population. A total of 127 moderate- high-risk families were screened for this mutation and it was also found in another high-risk family. All the families carrying the 936delAAAC mutation harboured part of a common haplotype shared by other reported carriers, suggesting a possible founder effect for this mutation.


Assuntos
Neoplasias da Mama Masculina/genética , Neoplasias da Mama/genética , Proteínas de Neoplasias/genética , Neoplasias Ovarianas/genética , Fatores de Transcrição/genética , Adulto , Proteína BRCA2 , Análise Mutacional de DNA , Feminino , Genótipo , Haplótipos , Humanos , Masculino , Pessoa de Meia-Idade , Linhagem , Fenótipo , Polimorfismo de Fragmento de Restrição , Espanha
8.
Rev Esp Cardiol ; 51 Suppl 3: 86-92, 1998.
Artigo em Espanhol | MEDLINE | ID: mdl-9717409

RESUMO

UNLABELLED: Coronary by-pass grafting is a well established procedure for ameliorating ischemic coronary disease. From time to time it is necessary to re-operate these patients. The objective of our paper is to present our experience in this field. Retrospective analysis of 128 patients operated on between February 1978 and November 1996, has been analyzed. The mean age was 57.4 +/- 0.7 years. 77.2 +/- 5 months elapsed between operations. Stable angina (20.4%) or unstable angina (76.3%), myocardial infarction (48%) and congestive heart failure (17%) were the predominant clinical manifestations. RESULTS: Hospital mortality was 10.9% (14 patients) and in the follow-up there were 16 deaths (14%). Perioperative myocardial infarction was the main cause of in-hospital mortality. In the follow-up there were 4 deaths due to myocardial infarction and another 4 patients died from neoplasms. Perioperative myocardial infarction was present in 9.3% (12 patients) IN CONCLUSION: a) Re-do coronary by-pass grafting is still a good procedure for solving myocardial ischemia in spite of a higher mortality and morbidity than in the original operation. b) There is no progression in the number of patients according to our experience, probably due to better techniques and the frequent actions by an intervention cardiologist. c) The long-term results are good enough, but with a higher mortality.


Assuntos
Ponte de Artéria Coronária , Adulto , Idoso , Causas de Morte , Ponte de Artéria Coronária/métodos , Ponte de Artéria Coronária/mortalidade , Feminino , Mortalidade Hospitalar , Humanos , Masculino , Pessoa de Meia-Idade , Reoperação , Estudos Retrospectivos
9.
Rev Stomatol Chir Maxillofac ; 98(6): 349-53, 1998 Feb.
Artigo em Francês | MEDLINE | ID: mdl-9533241

RESUMO

Ameloblastic fibro-odontoma is a rare odontogenic tumor. It is formed by proliferation of epithelial odontogenic elements combined with ectomesechimal tissue. The presence of dentine, enamel and osteoid like tissue can be identified. Cases of sarcomatous degeneration have been described. In this work, we present two new cases of ameloblastic fibro-odontoma, analyzing the most important aspects of their differential diagnosis, with a review of literature.


Assuntos
Neoplasias Maxilares/diagnóstico , Odontoma/diagnóstico , Adulto , Matriz Óssea/patologia , Calcinose/diagnóstico por imagem , Calcinose/patologia , Esmalte Dentário/patologia , Dentina/patologia , Diagnóstico Diferencial , Ectoderma/patologia , Feminino , Humanos , Masculino , Neoplasias Maxilares/diagnóstico por imagem , Neoplasias Maxilares/patologia , Mesoderma/patologia , Dente Serotino/diagnóstico por imagem , Odontoma/diagnóstico por imagem , Odontoma/patologia , Radiografia , Dente Impactado/diagnóstico por imagem
10.
Cancer Lett ; 123(2): 153-8, 1998 Jan 30.
Artigo em Inglês | MEDLINE | ID: mdl-9489482

RESUMO

BRCA1 accounts for nearly all families with multiple cases of both early onset breast and ovarian cancer and about 45% of families with breast cancer only. Although to date more than 200 distinct mutations have been described, several have been found to be recurrent in the gene. We have analyzed 87 Spanish breast/ovarian cancer families for the six most recurrent mutations in the BRCA1 gene. The analysis of the five exons where these mutations are located was made using the SSCP and sequenciation techniques. Four mutations were found in our families and only two carried one of the six mutations analyzed. In both cases the mutation identified was 185delAG. Our results suggest that these six mutations are not specially recurrent in the Spanish population and that differences in the geographical origin of the families can influence the type and proportion of mutations identified.


Assuntos
Neoplasias da Mama/genética , Genes BRCA1/genética , Neoplasias Ovarianas/genética , Adulto , Neoplasias da Mama Masculina/genética , DNA de Neoplasias/análise , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Mutação , Polimorfismo Conformacional de Fita Simples , Espanha
11.
J Med Genet ; 34(7): 592-3, 1997 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-9222971

RESUMO

A wide array of mutations now numbering more than 200 have been identified in the BRCA1 gene, one of the two breast cancer susceptibility genes identified so far. In addition, there have been several variants described but it is not known if they really represent functionally significant mutations of the BRCA1 gene. We report evidence to show that the duplication/ insertion of 12 base pairs in intron 20 could have a real effect on expression of the BRCA1 gene, although it was also present in 1% of our control population.


Assuntos
Proteína BRCA1/genética , Neoplasias da Mama Masculina/genética , Neoplasias da Mama/genética , Família Multigênica , Mutagênese Insercional , Adulto , Alelos , Feminino , Expressão Gênica , Humanos , Íntrons , Masculino , Neoplasias Ovarianas/genética , Polimorfismo Conformacional de Fita Simples , Neoplasias da Próstata/genética
12.
Br J Oral Maxillofac Surg ; 35(3): 180-4, 1997 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-9212295

RESUMO

The granular cell tumour (myoblastoma, Abrikosoff's tumour) and the congenital epulis in newborns (Neumann tumour) are two lesions rarely found in the oral cavity, whose histogenetic origin is highly controversial. This work analyses using immunohistochemical techniques 15 cases of myoblastomas and two of congenital epulis with different mono- and poly-clonal antibodies. Positive immunostaining was found for S-100 protein and neuron-specific enolase in all the cases of myoblastoma, and for vimentin and carcinoembryonic antigen in some cases. No immunoreactivity was observed for any of the other 13 antibodies used in congenital epulis.


Assuntos
Neoplasias Gengivais/patologia , Tumor de Células Granulares/patologia , Neoplasias Bucais/patologia , Actinas/análise , Adolescente , Adulto , Antígeno Carcinoembrionário/análise , Corantes , Desmina/análise , Feminino , Humanos , Imuno-Histoquímica , Recém-Nascido , Queratinas/análise , Masculino , Mucina-1/análise , Proteína Básica da Mielina/análise , Neoplasias de Tecido Muscular/patologia , Proteínas de Neurofilamentos/análise , Fosfopiruvato Hidratase/análise , Proteínas S100/análise , Vimentina/análise
13.
Ann Otolaryngol Chir Cervicofac ; 114(3): 76-9, 1997.
Artigo em Inglês | MEDLINE | ID: mdl-9295885

RESUMO

Central epithelial odontogenic ghost cell tumour, a neoplastic variant of calcifying odontogenic cyst, is a rare lesion with a very few cases published in the English literature. Histologically, the tumour consists of clusters of infiltrating odontogenic epithelium and ghost cells in varying numbers. We describe the first case of central epithelial odontogenic ghost cell tumour occurring in a pregnant woman and in which determination of bone densitometry in the preoperative panoramic radiographs has been performed. We have reviewed the literature available in English and compared it with our case.


Assuntos
Neoplasias Maxilares/patologia , Cisto Odontogênico Calcificante/patologia , Complicações Neoplásicas na Gravidez , Adulto , Feminino , Humanos , Neoplasias Maxilares/diagnóstico por imagem , Neoplasias Maxilares/cirurgia , Cisto Odontogênico Calcificante/diagnóstico por imagem , Cisto Odontogênico Calcificante/cirurgia , Gravidez , Radiografia
14.
An Otorrinolaringol Ibero Am ; 24(3): 255-68, 1997.
Artigo em Espanhol | MEDLINE | ID: mdl-9304350

RESUMO

Actinomycosis is an infectious disease that appears throught the world, in cattle and human beings. It is a chronic granulomatous and suppurative lesion, usually affecting the cervicofacial area. Definitive diagnosis, by culture or biopsy, is not always possible, so the clinician must suspect it by its clinical presentation. It is the purpose of this article to present the patients diagnosed and treated in our Department during the last 5 years, and to review the ideal therapy.


Assuntos
Actinomicose Cervicofacial/microbiologia , Actinomicose Cervicofacial/diagnóstico por imagem , Actinomicose Cervicofacial/tratamento farmacológico , Antibacterianos/uso terapêutico , Doxiciclina/uso terapêutico , Feminino , Humanos , Masculino , Mandíbula/diagnóstico por imagem , Mandíbula/microbiologia , Pessoa de Meia-Idade , Radiografia
15.
Cancer Lett ; 121(2): 115-8, 1997 Dec 23.
Artigo em Inglês | MEDLINE | ID: mdl-9570347

RESUMO

The recently isolated gene BRCA2 is responsible for about 45% of familial breast cancer and the majority of male breast cancer families. We have screened 12 high risk breast/ovarian Spanish families for mutations in BRCA2, using SSCP followed by direct sequencing. We have found mutations in four of our 12 families (33.3%), including two with male breast cancer. Three of the mutations were frameshift and one was a missense. Two of the mutations have been previously published and two are new mutations.


Assuntos
Neoplasias da Mama Masculina/genética , Neoplasias da Mama/genética , Mutação da Fase de Leitura , Genes BRCA1 , Neoplasias Ovarianas/genética , Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Mutação , Linhagem , Fenótipo , Fatores de Risco , Espanha
16.
Circulation ; 93(4): 753-62, 1996 Feb 15.
Artigo em Inglês | MEDLINE | ID: mdl-8641005

RESUMO

BACKGROUND: Some patients with an automatic implantable cardioverter-defibrillator (ICD) suffer multiple appropriate, consecutive, high-energy discharges (MCDs) during follow-up. Such events might represent resistant ventricular arrhythmias and might have prognostic significance. METHODS AND RESULTS: Eighty consecutive patients with an ICD were followed up for up to 82 months (mean, 21 +/- 19 months). Thirty-eight patients had survived an out-of-hospital cardiac arrest and 42 had recurrent ventricular tachycardia. During follow-up, 16 patients had MCD (group A), 26 patients had episodes of single appropriate discharges (group B), and 38 patients had no appropriate discharges (group C). Group A patients had worse functional status (P = .001), lower left ventricular ejection fractions (LVEFs) (P = .001), and lower survival rates (log rank, P = .003) than the remaining two groups of patients. Cox analysis showed LVEF (P = .001) to be an independent predictor of MCD. Independent predictors of death or heart transplant were MCD (P = .001), female sex (P = .001), age (P = .001), history of cardiac arrest (P = .003), and functional status (P = .003). The only independent predictor of total mortality was female sex (P = .002). Independent predictors of cardiac death were MCD (P = .007) and female sex (P = .018). Independent predictors of arrhythmic death were age (P = .001), female sex (P = .02), and MCD (P = .023). CONCLUSIONS: In patients with an ICD, the development of MCD is an independent predictor of cardiac and arrhythmic mortality. If this finding is confirmed in larger studies, it may help to identify patients in whom other therapeutic alternatives, ie, heart transplantation, should be considered during follow-up after ICD implantation.


Assuntos
Desfibriladores Implantáveis/efeitos adversos , Taquicardia Ventricular/terapia , Idoso , Morte Súbita Cardíaca/etiologia , Morte Súbita Cardíaca/prevenção & controle , Eletrônica Médica , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Prognóstico , Estudos Prospectivos , Estudos Retrospectivos , Taxa de Sobrevida , Taquicardia Ventricular/mortalidade , Taquicardia Ventricular/fisiopatologia , Função Ventricular Esquerda
17.
Ann Thorac Surg ; 60(5): 1226-9, 1995 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-8526604

RESUMO

BACKGROUND: Massive calcification of the atrial walls ("porcelain atrium") is a rare condition that usually has been reported as an incidental radiologic findings. METHODS: Between January 1988 and June 1993, 971 patients underwent valvular operation at our institution; 21 patients showed extensive calcification of the left atrium. In 8 patients the calcification was massive, involving almost all the atrial surface. The diagnoses were established by radiology and were confirmed at operation. The mean age of these patients (4 men, 4 women) was 55 +/- 9.6 years. All had rheumatic valve disease, were on atrial fibrillation, and had undergone at least one operation previously. Pulmonary artery pressure was severely increased, even up to systemic levels, in all patients except 1. Total endoatriectomy of the left atrium and mitral valve replacement were performed. No patient was lost during the follow-up. RESULTS: Hospital mortality rate was 12.5% (1 patient) and 2 patients died in the late postoperative period. None of these deaths are attributable to the surgical procedure. CONCLUSIONS: In toto endoatriectomy of a massively calcified atrium is an easy to perform technique that helps to replace the mitral valve and close the atrial wall.


Assuntos
Calcinose/cirurgia , Cardiomiopatias/cirurgia , Cardiopatia Reumática/cirurgia , Adulto , Idoso , Calcinose/complicações , Calcinose/diagnóstico por imagem , Cardiomiopatias/complicações , Cardiomiopatias/diagnóstico por imagem , Feminino , Seguimentos , Átrios do Coração , Próteses Valvulares Cardíacas , Mortalidade Hospitalar , Humanos , Masculino , Pessoa de Meia-Idade , Pressão Propulsora Pulmonar , Radiografia , Cardiopatia Reumática/complicações
18.
Ann Thorac Surg ; 60(3): 687-9, 1995 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-7677503

RESUMO

A 37-year-old man who had suffered a thoracic trauma presented night release of whitish urine 2 years later. Thoracic computed tomography and aortography demonstrated an aneurysm of the thoracic aorta. Lymphography confirmed the compression of the thoracic duct by the aneurysm. After surgical repair the patient has remained asymptomatic.


Assuntos
Aneurisma da Aorta Torácica/complicações , Aneurisma da Aorta Torácica/cirurgia , Quilo , Adulto , Aneurisma da Aorta Torácica/diagnóstico por imagem , Aortografia , Humanos , Doenças Linfáticas/diagnóstico por imagem , Doenças Linfáticas/etiologia , Masculino , Ducto Torácico/diagnóstico por imagem , Ducto Torácico/patologia , Tomografia Computadorizada por Raios X , Urina
19.
Int J Paediatr Dent ; 5(3): 181-6, 1995 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-9601241

RESUMO

The ameloblastic fibroma is an odontogenic tumour with an unusual presentation. It is considered to have both epithelial and mesenchymal elements, but it lacks any calcified dental structures. Two new cases are presented. The first of these began as a mandibular tumour whereas the second was discovered by chance. The radiographic finding in each case was a unilocular cystic radiolucency. Treatment consisted of excisional biopsy by enucleation in both patients. Histopathological findings were consistent with ameloblastic fibroma.


Assuntos
Neoplasias Mandibulares/patologia , Tumores Odontogênicos/patologia , Criança , Humanos , Masculino , Neoplasias Mandibulares/terapia , Tumores Odontogênicos/terapia
20.
Rev Esp Cardiol ; 48(5): 362-4, 1995 May.
Artigo em Espanhol | MEDLINE | ID: mdl-7792431

RESUMO

The amount of transplants has gone through a remarkable increase during the last years. As a result, congenital anomalies of little prevalence appear more and more often while performing the transplants. The persistence of upper cava vein is one of them and, if not linked to other anomalies, it usually remains unnoticed. This article presents a case of an orthotopic cardiac transplant in a patient with an upper cava vein duplication not diagnosed before undergoing surgery, and it compares the way it was handled to diverse techniques previously described.


Assuntos
Transplante de Coração , Veia Cava Superior/anormalidades , Adulto , Transplante de Coração/métodos , Humanos , Masculino
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