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1.
Chinese Journal of Surgery ; (12): 324-329, 2006.
Article in Chinese | WPRIM | ID: wpr-317158

ABSTRACT

<p><b>OBJECTIVE</b>To inquiry into clinical-pathological factors influencing cytological accuracy of pancreatic head lesions.</p><p><b>METHODS</b>Cytology was retrospectively evaluated in 94 inpatients with a mass in head of pancreas existing with chronic pancreatitis in the past decade, the results of cytology were compared with clinical pathology or clinical follow-up to estimate the value and accuracy of cytology in detecting pancreatic cancer. Pancreatic clinical-pathology includes size of mass and component of mass which was composed of cancerous mode of development including shape of conglomeration, nest and pervasion, and pancreatic ductal epithelium inside the vicinity of 1 cm around the mass. Pancreatic ductal epithelium were divided into PanIN1, PanIN2 and PanIN3 three types according to classified criterion of pancreatic intraepithelial neoplasia (PanIN).</p><p><b>RESULT</b>Forty-six patients were pathologically diagnosed as pancreatic cancer and five patients as chronic pancreatitis, accordingly, 29 malignant, 5 suspicious, 10 atypical hyperplasia among of them 5 malignant, 3 hyperplastic ductal epithelium, 1 nondiagnostic results due to interfered by blood and 3 insufficient specimens. 43 patients were clinically diagnosed as chronic pancreatitis. Cytologic evaluation of pancreatic cancer has an 84.2% accuracy less than or equal to 2.5 cm and 71.9% larger than 2.5 cm. Shape of conglomeration, and nest have more accurate than pervasion in cytological diagnosis.</p><p><b>CONCLUSIONS</b>Cancerous mode of development is a vital factor influencing accuracy of cytology, cytological estimation of atypical hyperplasia and is still waiting for further investigation.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Biopsy, Needle , Chi-Square Distribution , False Negative Reactions , False Positive Reactions , Pancreas , Pathology , Pancreatic Neoplasms , Pathology , Pancreatitis, Chronic , Pathology , Retrospective Studies , Sensitivity and Specificity
2.
Chinese Journal of Oncology ; (12): 433-437, 2006.
Article in Chinese | WPRIM | ID: wpr-236923

ABSTRACT

<p><b>OBJECTIVE</b>To explore the significance of mitochondrial D-loop alterations in hyperplastic pancreatic ductal cells in vicinity of pancreatic cancer coexisting with chronic pancreatitis.</p><p><b>METHODS</b>Malignant lesions and foci of pancreatic ductal intraepithelial neoplasia of the pancreas and paired normal gastric mucosal epithelial cells from the same patients, respectively, were assessed by polymerase chain reaction. Somatic point mutations and sequence variants of D-loop were searched by direct sequencing of the mitochondrial genome. D-loops were sequenced by BLAST to identify their mutations.</p><p><b>RESULTS</b>Eleven of 12 pancreatic cancers displayed at least one D-loop variants and one tumor presented heteroplasmy. There was an apparent increase in incidence of D-loop mutational rate from PanIN1 (33.3%) to PanIN3 (75%, P < 0.01).</p><p><b>CONCLUSION</b>Mitochondrial D-loop alterations in the pancreas occur in the earliest premalignant lesions and exhibite an increasing occurence that parallels histological severity. These alterations may serve as a valuable marker to follow the histopathological progression of the lesions. Large number of further studies are required to clarify clinical implications of the mitochondrial DNA alterations.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Adenoma , Genetics , Base Sequence , DNA, Mitochondrial , Genetics , Epithelial Cells , Metabolism , Pathology , Mutation , Pancreatic Ducts , Metabolism , Pathology , Pancreatic Neoplasms , Genetics , Pancreatitis, Chronic , Genetics , Precancerous Conditions , Genetics , Sequence Analysis, DNA
3.
Chinese Journal of Epidemiology ; (12): 339-343, 2005.
Article in Chinese | WPRIM | ID: wpr-331881

ABSTRACT

<p><b>OBJECTIVE</b>To understand the environmental risk factors on attempted suicide, and to study the interaction between factors as gene polymorphism of catechol-O-methyltransferase (COMT) associated to attempted suicide.</p><p><b>METHODS</b>Paired case-control study of 205 suicide attempters (89 male, 116 female) and molecular biological techniques were used to study the relation between gene polymorphism of COMT, environmental factors and the rate of attempted suicide. Controls were paired with cases according to the same gender, similar age (no more than 3 years) and in the same district.</p><p><b>RESULTS</b>There were no significant differences in gene types and gene frequency between case and control groups. Multivariate conditional logistic regression model analysis showed that COMT Val/Val 158/108, low education level, cigarette smoking, emotional conflicts, psychologic disorders and depression were risk factors of attempted suicide with OR values as 2.43 (95% CI: 1.10 - 5.40), 5.70 (95% CI: 1.88 - 17.27), 3.54 (95% CI: 1.02 - 12.36), 10.96 (95% CI: 4.74 - 25.34), 6.35 (95% CI: 1.68 - 24.05) and 11.30 (95% CI: 4.58 - 27.89) respectively. There was no first level interaction between any two risk factors.</p><p><b>CONCLUSION</b>The study supported that low education level, cigarette smoking, affective conflicts, psychiatric disorders, depression were risk factors of attempted suicide and COMT Val/Val 158/108 was suspected to be a susceptible gene type of attempted suicide but needs further study. The study also suggested that 116 bp in gene atlas be possibly correlated to high activity of COMT.</p>


Subject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Case-Control Studies , Catechol O-Methyltransferase , Genetics , China , Epidemiology , Depression , Logistic Models , Polymorphism, Genetic , Risk Factors , Smoking , Suicide, Attempted
4.
Chinese Journal of Epidemiology ; (12): 794-798, 2004.
Article in Chinese | WPRIM | ID: wpr-247472

ABSTRACT

<p><b>OBJECTIVE</b>To determine the risk factors in the development of central nervous system (CNS) congenital malformations.</p><p><b>METHODS</b>A hospital-based 1:2 matched case-control study was conducted. Each case was matched with two normal controls on sex and residential area, date of birth, within half a year. By means of simple and multivariable conditional logistic regression, 48 factors were analyzed.</p><p><b>RESULTS</b>Maternal exposure to pesticide or having cold with fever, family history of positive congenital malformations, preference eating pickled vegetables, negative life events, large consumption of meat, eggs, beans and milk during pregnancy and paternal exposure to poisonous chemicals were significantly associated with CNS congenital malformations, with odds ratios 16.471, 12.621, 10.246, 7.274, 3.730, 0.229, 5.616, respectively.</p><p><b>CONCLUSIONS</b>Maternal exposure to pesticides, cold with fever, positive congenital malformations family history, preference of eating pickled vegetables, negative life events during pregnancy, and paternal exposure to poisonous chemicals were the key risk factors contributing to CNS congenital malformations, while maternal exposure to big consumption of meat, eggs, beans and milk during pregnancy was protective factors that reducing CNS congenital malformations.</p>


Subject(s)
Adult , Female , Humans , Male , Pregnancy , Case-Control Studies , China , Epidemiology , Environmental Exposure , Maternal Exposure , Nervous System Malformations , Epidemiology , Neural Tube Defects , Epidemiology , Paternal Exposure , Risk Factors
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