47 research outputs found

    Evaluation of seven tumour markers in pleural fluid for the diagnosis of malignant effusions

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    Carcinoembryonic antigen (CEA), carbohydrate antigens 15–3, 19–9 and 72–4 (CA 15–3, CA 19–9 and CA 72–4), cytokeratin 19 fragments (CYFRA 21–1), neuron-specific enolase (NSE) and squamous cell carcinoma antigen (SCC) were evaluated in pleural fluid for the diagnosis of malignant effusions. With a specificity of 99%, determined in a series of 121 benign effusions, the best individual diagnostic sensitivities in the whole series of 215 malignant effusions or in the subgroup of adenocarcinomas were observed with CEA, CA 15–3 and CA 72–4. As expected, a high sensitivity was obtained with SCC in squamous cell carcinomas and with NSE in small-cell lung carcinomas. CYFRA and/or CA 15–3 were frequently increased in mesotheliomas. Discriminant analysis showed that the optimal combination for diagnosis of non-lymphomatous malignant effusions was CEA + CA 15–3 + CYFRA + NSE: sensitivity of 94.4% with an overall specificity of 95%. In malignant effusions with a negative cytology, 83.9% were diagnosed using this association. The association CYFRA + NSE + SCC was able to discriminate adenocarcinomas from small-cell lung cancers. Regarding their sensitivity and their complementarity, CEA, CA 15–3, CYFRA 21–1, NSE and SCC appear to be very useful to improve the diagnosis of malignant pleural effusions. © 1999 Cancer Research Campaig

    Anticipating the Unpredictable: A Review of Antimicrobial Stewardship and Acinetobacter Infections

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    Urinothorax: an unexpected cause of severe dyspnea

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    Respiratory Hoover′s sign

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    4. Section of Preventive Medicine

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    have been associated with outbreaks and multidrug resistance. We performed a retrospective thirteen-year surveillance study (1993 of the available isolates from 332 cases of tuberculosis tested of an immigrant patient from Senegal with pulmonary tuberculosis. The strain was not drug resistant and besides six close contact persons that were infected no secondary cases of this strain were low and there is no evidence of transmission or higher virulence. Molecular epidemiology studies have revealed a genotype of M. tuberculosis strains that seem to possess selective advantages compared with other strains, have increased virulence and are sometimes associated with multidrug resistance [1,2]. This it is widespread around the world. The fact that this family of strains is widespread and, in some situations, associated with multidrug resistance has led to concern that these strains may be spreading the study of trends over time is of great interest. However, report
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