Diagnosis of new occupational lung tumor in Guangdong Province / 中国职业医学

OBJECTIVE: To summarize and analyze the diagnostic ideas of new occupational lung tumors in Guangdong Province.METHODS: According to the Law of the People′s Republic of China on the Prevention and Control of Occupational Disease and the GBZ 94-2002 Diagnostic Criteria of Occupational Cancer, the key diagnostic points of 6 new occupational lung tumors diagnosed in Guangdong Province from 2010 to 2011 were analyzed. RESULTS: There were 9 cases of 6 new kinds of new occupational tumors were diagnosed in Guangdong Province in 2010-2011. The cases included 3 occupational lung cancer of coke oven workers, 2 occupational lung cancer caused by asbestos, 1 occupational mesothelioma caused by asbestos, 1 occupational lung cancer caused by arsenate, 1 occupational lung cancer caused by chromate salt, and 1 occupational lung cancer caused by asphalt. During the process, the diagnosis was based on the principles of the comprehensive analysis and the attribution diagnosis, combined with occupational history, occupational disease hazard exposure history, clinical data and auxiliary examination results. If the patients were diagnosed with a primary tumor, the patients′ exposure history to occupational carcinogens should be tracked, traced and confirmed, and the diagnosis should be confirmed by referring to the list of occupational carcinogens and literature reports of the International Labor Organization, and not limited to only the personnel in a particular industry. CONCLUSION: During the diagnostic process of occupational tumors, attention should be paid to confirm the exposure history of occupational carcinogen. The key is to determine the exposure of corresponding occupational carcinogen, the route and the time of exposure and the incubation period.

The observation of surface morphology of enamal and temperature of dental pulp cavity in vitro after irradiated by Er:YAG laser / 华西口腔医学杂志

<p><b>OBJECTIVE</b>To observe the changes of surface morphology and temperature of dental pulp cavity in vitro after irradiated by Er:YAG laser with different energy and irradiation time.</p><p><b>METHODS</b>All of the 96 samples from 24 teeth in vitro were collected from dental clinical departments then divided into two groups (group A and group B) randomly. We chose the energy of 20 Hz, and 1, 2, 3, 4, 5, 6 W to treat the samples in group A and group B and the irradiation time was 10s or 20s. We recorded the temperature changes of dental pulp cavity by digital thermometer and observe the morphology of tooth enamel by scanning electron microscope (SEM).</p><p><b>RESULTS</b>With the extension of irradiation time and increasing of energy, the temperatures of dental pulp cavity were significantly increased after the treatment of Er: YAG laser. The two groups of tooth enamel surface morphology were changed after irradiated by Er: YAG laser with different energy and irradiation time. However, there was no melting and carbonation on the surface of tooth enamel after the treatment of Er:YAG laser in two groups.</p><p><b>CONCLUSION</b>The temperatures of dental pulp cavity were increased after irradiated by increasing laser energy density fom 1 W to 6 W. No melting or carbonized phenomenon was found in enamel within the energy of 1 W to 6 W. All the data would provide evidences for clinical treatment of cavity.</p>

Diagnostic Value of Detection of 16S rRNA Gene of Pathogens from Blood by PCR / 中华医院感染学杂志

OBJECTIVE To explore study a method for rapid detection of bacterial infection in clinic to diagnose septicemia early.METHODS 16S rRNA gene of ten bacterial species was amplified with PCR,by using human genome DNA,HBV-DNA and Candida albicans as comparison.The sensitivity test was done by the method of gradual dilution of Escherichia coli.RESULTS The bacterial species were amplified and the products were 371 bp,but human genome DNA,HBV-DNA and C.albicans showed no amplification products.Sensitivity test showed that it could detect as low as 1.5?104/L of E.coli.CONCLUSIONS The method is rapid and highly specific and sensitive in detecting the existence of bacterial 16S rRNA gene.