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1.
Zhongguo Yi Liao Qi Xie Za Zhi ; 31(5): 324-7, 2007 Sep.
Artículo en Zh | MEDLINE | ID: mdl-18161367

RESUMEN

The positioning error in radiotherapy is one of the most important factors that influence the location precision of the tumor. Based on the CT-on-rails technology, this paper describes the research on measuring the positioning error in radiotherapy by comparing the planning CT images with the treatment CT images using 3-dimension (3D) methods. It can help doctors to measure positioning errors more accurately than 2D methods. It also supports the powerful 3D interaction such as drag-dropping, rotating and picking-up the object, so that doctors can visualize and measure the positioning errors intuitively.


Asunto(s)
Imagenología Tridimensional , Radioterapia/métodos , Humanos
2.
Zhongguo Yi Liao Qi Xie Za Zhi ; 31(6): 400-3, 2007 Nov.
Artículo en Zh | MEDLINE | ID: mdl-18269035

RESUMEN

Because of different display parameters and other factors, digital medical images present different display states in different section offices of a hospital. Based on CPI integration profile of IHE, this paper implements the consistent presentation of medical images, and it is helpful for doctors to carry out medical treatments of teamwork.


Asunto(s)
Diagnóstico por Imagen , Sistemas Integrados y Avanzados de Gestión de la Información , Computación en Informática Médica/normas , Simulación por Computador
3.
World J Gastroenterol ; 11(14): 2055-60, 2005 Apr 14.
Artículo en Inglés | MEDLINE | ID: mdl-15810068

RESUMEN

AIM: Microsatellites are the repeated DNA sequences scattered widely within the genomes and closely linked with many important genes. This study was designed to characterize the changes of microsatellite DNA loss of heterozygosity (LOH) in esophageal carcinogenesis. METHODS: Allelic deletions in 32 cases of matched precancerous, cancerous and normal tissues were examined by syringe microdissection under an anatomic microscope and microsatellite polymorphism analysis using 15 polymorphic markers on chromosomes 3p, 5q, 6p, 9p, 13q, 17p, 17q and 18q. RESULTS: Microsatellite DNA LOH was observed in precancerous and cancerous tissues, except D9S1752. The rate of LOH increased remarkably with the lesions progressed from basal cell hyperplasia (BCH) to squamous cell carcinoma (SCC) (P<0.05). Three markers, D9S171, D13S260 and TP53, showed the highest incidence of LOH (>60%). LOH loci were different in precancerous and cancerous tissues. LOH in D3S1234 and TP53 was the common event in different lesions from the same patients. CONCLUSION: Microsatellite DNA LOH occurs in early stage of human esophageal carcinogenesis, even in BCH. With the lesion progressed, gene instability increases, the accumulation of this change may be one of the important mechanisms driving precancerous lesions to cancer.


Asunto(s)
Carcinoma Basocelular/genética , Carcinoma de Células Escamosas/genética , Neoplasias Esofágicas/genética , Pérdida de Heterocigocidad , Adulto , Anciano , Carcinoma Basocelular/epidemiología , Carcinoma Basocelular/patología , Carcinoma de Células Escamosas/epidemiología , Carcinoma de Células Escamosas/patología , China/epidemiología , Neoplasias Esofágicas/epidemiología , Neoplasias Esofágicas/patología , Femenino , Humanos , Incidencia , Masculino , Repeticiones de Microsatélite , Persona de Mediana Edad , Estadificación de Neoplasias
4.
World J Gastroenterol ; 10(22): 3365-8, 2004 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-15484320

RESUMEN

AIM: To characterize the protein files in blood from same patients with esophageal squamous cell carcinoma (ESCC) before and after operation at the high-incidence area for ESCC in Henan Province, China. METHODS: Two-dimensional electrophoresis, silver staining and ImageMaster 2-DE analysis software were applied to the determination of protein files in the blood obtained from normal controls and ESCC patients before and after operation. RESULTS: A total of 655, 662 and 677 protein spots were identified, respectively, from the normal controls and ESCC patients before and after operation. No significant difference in the number of protein spots was observed between the normal group and ESCC patients. A total of seven protein spots were identified with a dramatic difference among the samples before and after operation. Six protein spots were up-regulated and one protein spot was down-regulated in the group after operation compared with those in normal and before operation. Three protein spots were further characterized by matrix-assisted laser desorption/ionization time of flying mass spectrometry (MALDI-TOF-MS). The proteins from these three spots were identified as serum amyloid A (SAA), amyloid related serum protein and haptoglobin. CONCLUSION: Serum amyloid A, amyloid related serum protein and haptoglobin may be related with ESCC and/or surgery. The significance of these proteins needs to be further characterized. The present study provides informative data for the establishment of serum protein profiles related with ESCC.


Asunto(s)
Carcinoma de Células Escamosas/sangre , Carcinoma de Células Escamosas/cirugía , Neoplasias Esofágicas/sangre , Neoplasias Esofágicas/cirugía , Proteómica , Anciano , Proteínas Sanguíneas/análisis , Carcinoma de Células Escamosas/epidemiología , China/epidemiología , Electroforesis en Gel Bidimensional , Neoplasias Esofágicas/epidemiología , Femenino , Humanos , Incidencia , Masculino , Persona de Mediana Edad , Tinción con Nitrato de Plata , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción
5.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 21(6): 625-8, 2004 Dec.
Artículo en Zh | MEDLINE | ID: mdl-15583998

RESUMEN

OBJECTIVE: To characterize the profiles of chromosome imbalance in esophageal squamous cell carcinoma (SCC) and gastric cardia adenocarcinoma (GCA) from the high incidence area in Henan. METHODS: Chromosomal aberrations of 37 samples of SCC and 30 GCA were analyzed by comparative genomic hybridization comparative genomic hybridization (CGH). RESULTS: It was found that the most frequently detected gains were on chromosome arm 8q (78%), and followed by 3q, 5p, 6q and 7p. The most frequent loss was found on 3p (57%), and followed by 8p, 9q and 11q in SCC. For GCA, the most frequent gain was found on chromosome arm 20q (43%), and followed by 6q, 8q and 6p. The most frequent loss was on the chromosome 17p (57%), and followed by 19p, 1p and 4p. CONCLUSION: The present findings demonstrate that gains of 8q, 3q and 5p, and losses of 3p, 8p, and 9q are characteristic profile of chromosome imbalance in SCC, and the gains of 20q, 6q and losses of 17p, 19p and 1p are characteristic profile of chromosome imbalance in GCA, which provide important theoretic information for identifying and cloning novel SCC/GCA-related genes.


Asunto(s)
Cardias , Neoplasias Esofágicas/genética , Amplificación de Genes , Eliminación de Gen , Neoplasias Gástricas/genética , Adenocarcinoma/genética , Carcinoma de Células Escamosas/epidemiología , Carcinoma de Células Escamosas/genética , Cromosomas Humanos Par 17 , Cromosomas Humanos Par 20 , Cromosomas Humanos Par 3 , Cromosomas Humanos Par 8 , ADN de Neoplasias/genética , Neoplasias Esofágicas/epidemiología , Humanos , Hibridación de Ácido Nucleico/métodos , Neoplasias Gástricas/epidemiología
6.
Cancer Lett ; 2013 Sep 26.
Artículo en Inglés | MEDLINE | ID: mdl-15882929

RESUMEN

This article has been withdrawn at the request of the author(s) and/or editor. The Publisher apologizes for any inconvenience this may cause. The full Elsevier Policy on Article Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy.

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