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2D and 3D refraction-based visualization of breast cancer for early clinical check 被引量:2
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作者 Masami ANDO Anton MAKSIMENKO +9 位作者 Tetsuya YUASA Eiko HASHIMOTO Katsuhito YAMASAKI Shu IHIHARA Hiroshi SUGIYAMA Tokiko ENDO LI Gang CHEN Zhihua Kazuyuki HYODO Ei UENO 《Nuclear Science and Techniques》 SCIE CAS CSCD 2006年第6期389-395,共7页
Ductal carcinoma in-situ (DCIS) has been visualized by 2D XDFI (X-ray dark-field imaging) and further by a 3D X-ray CT, and the data was acquired by the X-ray optics DEI (diffraction-enhanced imaging). A newly made al... Ductal carcinoma in-situ (DCIS) has been visualized by 2D XDFI (X-ray dark-field imaging) and further by a 3D X-ray CT, and the data was acquired by the X-ray optics DEI (diffraction-enhanced imaging). A newly made algorithm was used for CT. Data of 900 projections with interval of 0.2 degrees were used. Ductus lactiferi, microcalci-fication in a 3D form have been clearly visible. The spatial resolution available was approximately 30μm. 展开更多
关键词 折射 乳腺癌 临床检查 CT
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Pulmonary nocardiosis with bloodstream infection diagnosed by metagenomic next-generation sequencing in a kidney transplant recipient:A case report
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作者 Zhen-Feng Deng Yan-Jiao Tang +3 位作者 Chun-Yi Yan Zi-Qian Qin Ning Yu Xiong-Bo Zhong 《World Journal of Clinical Cases》 SCIE 2023年第7期1634-1641,共8页
BACKGROUND Pulmonary nocardiosis is difficult to diagnose by culture and other conventional testing,and is often associated with lethal disseminated infections.This difficulty poses a great challenge to the timeliness... BACKGROUND Pulmonary nocardiosis is difficult to diagnose by culture and other conventional testing,and is often associated with lethal disseminated infections.This difficulty poses a great challenge to the timeliness and accuracy of clinical detection,especially in susceptible immunosuppressed individuals.Metagenomic nextgeneration sequencing(mNGS)has transformed the conventional diagnosis pattern by providing a rapid and precise method to assess all microorganisms in a sample.CASE SUMMARY A 45-year-old male was hospitalized for cough,chest tightness and fatigue for 3 consecutive days.He had received a kidney transplant 42 d prior to admission.No pathogens were detected at admission.Chest computed tomography showed nodules,streak shadows and fiber lesions in both lung lobes as well as right pleural effusion.Pulmonary tuberculosis with pleural effusion was highly suspected based on the symptoms,imaging and residence in a high tuberculosisburden area.However,anti-tuberculosis treatment was ineffective,showing no improvement in computed tomography imaging.Pleural effusion and blood samples were subsequently sent for mNGS.The results indicated Nocardia farcinica as the major pathogen.After switching to sulphamethoxazole combined with minocycline for antinocardiosis treatment,the patient gradually improved and was finally discharged.CONCLUSION A case of pulmonary nocardiosis with an accompanying bloodstream infection was diagnosed and promptly treated before the dissemination of the infection.This report emphasizes the value of mNGS in the diagnosis of nocardiosis.mNGS may be an effective method for facilitating early diagnosis and prompt treatment in infectious diseases,which overcomes the shortcomings of conventional testing. 展开更多
关键词 Nocardia farcinica NOCARDIOSIS Metagenomic next-generation sequencing DIAGNOSIS Case report
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The next generation of cancer management
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作者 Wayne W.Grody 《Cancer Biology & Medicine》 SCIE CAS CSCD 2016年第1期1-2,共2页
As readers of Cancer Biology and Medicine well know,there has been a seismic shift in human molecular biology over the past few years,as momentous in its own way as the discovery of the double-helical structure of DNA... As readers of Cancer Biology and Medicine well know,there has been a seismic shift in human molecular biology over the past few years,as momentous in its own way as the discovery of the double-helical structure of DNA by Watson and Crick 60 years ago,the elucidation of the genetic code shortly thereafter,the advent of recombinant DNA and gene 展开更多
关键词 DNA重组 管理 癌症 聚合酶链反应 基因编码 肿瘤生物学 分子生物学 双螺旋结构
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中国结直肠癌错配修复功能缺陷患病率较低:一项多中心研究 被引量:1
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作者 Wu Jiang Qiao-Qi Sui +12 位作者 Wen-Liang Li Chuan-Feng Ke Yi-Hong Ling Le-En Liao Zhu Zhu Mu-Yan Cai Jun Luo Lin-Lin Mao Hui-Zhong Zhang De-Sen Wan Zhi-Zhong Pan Hai-Xing Ju Pei-Rong Ding 《Gastroenterology Report》 SCIE EI 2020年第5期399-403,I0003,共6页
背景:尽管错配修复功能缺陷(dMMR)检测已被推荐用于所有结直肠癌患者,但其用于中国人群中仍缺乏数据支持。因此,我们调查了一个大型中国结直肠癌队列中dMMR的患病率及其临床病理特征。方法:纳入2010年8月至2016年9月间在四家医疗中心就... 背景:尽管错配修复功能缺陷(dMMR)检测已被推荐用于所有结直肠癌患者,但其用于中国人群中仍缺乏数据支持。因此,我们调查了一个大型中国结直肠癌队列中dMMR的患病率及其临床病理特征。方法:纳入2010年8月至2016年9月间在四家医疗中心就治的7,373例结直肠癌患者,记录其基线资料和病理特征,并比较MLH1/PMS2表达缺失(dMLH1/PMS2)与MSH2/MSH6表达缺失(dMSH2/MSH6)患者的临床病理特征。结果:本组病例中654例(8.9%)被判定为dMMR,其中401例(61.3%)为男性,中位发病年龄55岁(范围:22-87岁);355例(54.3%)为II期肠癌(AJCC 8版)。dMLH1/PMS2和dMSH2/MSH6的出现率分别为51.5%(337/654)和25.1%(164/654)。与dMSH2/MSH6组相比,dMLH1/PMS2组患者年龄较大(57岁vs 52岁,P<0.001),女性占比更高(45.7%vs 31.5,P=0.004),肿瘤更多位于右半结肠(59.0%vs 47.6%,P=0.015),具有肿瘤家族史的比例较低(29.7%vs 43.3%,P=0.003)。结论:中国结直肠癌人群dMMR患病率偏低,尤其是dMLH1/PMS2。不同类型dMMR患者有着不同的临床病理特征。 展开更多
关键词 PREVALENCE mismatch repair deficiency colorectal cancer
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