1.To further improve the effects of surgical treatment for hilar cholangiocarcinoma.
Xiao-ping CHEN ; Zhi-yong HUANG
Chinese Journal of Surgery 2009;47(15):1121-1122
Bile Duct Neoplasms
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pathology
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surgery
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Bile Ducts, Intrahepatic
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Cholangiocarcinoma
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pathology
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surgery
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Hepatectomy
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methods
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Hepatic Artery
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pathology
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surgery
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Humans
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Lymph Node Excision
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methods
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Portal Vein
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pathology
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surgery
2.Application of ultrasound guided mammotome minimally invasive biopsy system in 42 cases of breast mass
Linjun YANG ; Ping YIN ; Yong CHEN
China Oncology 2001;0(03):-
Purpose:To evaluate the Application of Ultrasound Guided Mammotome Minimallay Invasive Biopsy System in diagnosis and treatment of breast masses. Methods:68 breast lesions in 42 patients were performed by Ultrasound Guided Mammotome Minimallay Invasive Biopsy System in order to evaluateits diagnostic and therapeutic ifficacy. Results:40 lesions were diagnosed as fibroadenoma , 19 lesions as fibroadenomatoid hyperplasia, 7 lesions as breast adenosis,2 lesions diagnosed as galactocele in operation but fibre and fat tissue after operation by pathology. 67 lesions were excised by mammotome system. 1 lesion was stopped duete hmorrage,1 case had serious hematoma. 1 case had machine failure but was resolved. The excision times were on the average 28 in every lesion,the lengh of incision is only 3mm,and the duration of operation was 30 minutes. No evidence of recurrence was found by physical examination and the ultrasound evaluation during the follow up 1~6 monthes. Conclusions:Ultrasound guided mammotome minimallay invasive biopsy system excision for benign breast mass was complete and the postoperative breast appearance was satisfactory.
4.Study on the polymorphisms and promoter methylation and expression of the glutathione S-transferases P1 gene in hepatocellular carcinoma
You-Cai ZHANG ; Yong-Ping CHEN ; Jin-Xia CHEN ;
Chinese Journal of Digestion 2001;0(07):-
Objective To study the relationships between hepatocellular carcinoma (HCC) and the polymorphisms,promoter methylation,and expression of glutathione S-transferases P1 gene (GST) P1 gene.Methods Using methylation-special PCR (MSP),the methylated status of CpG islands of GSTP1 gene in tumor tissues of 53 HCC and its adjacent nontumor tissues were studied.The enzyme activities of GSTP1 were evaluated by ultraviolet colormetry.And using PCR-RFLP,the genetic polymorphisms of the GSTP1 genes of 74 healthy controls and 53 HCC patients were studied.Results The diffe-rences of the frequency of GSTP1 Ile/Ile,Ile/Val and Val/Val genotypes between HCC patients and the normal controls did not reach statistical significance (X~2=0.84,v=2,P=0.656).The frequency of methyla- tion of CpG islands of GSTP1 gene was significantly higher among the HCC tumor tissues when com- pared to the corresponding nontumor tissues (X~2=19.08,P<0.001),and significantly higher in stageⅢ-Ⅳcases when compared to the stageⅠ-Ⅱcases (X~2=4.84,P=0.028).GSTP1 enzyme activities of cytoplasm in tumor cells were lower significantly than that in the adjacent nontumor tissues (t=2.49, P=0.014),and significantly higher in stageⅠ-Ⅱcases when compared to the stageⅢ-Ⅳcases (t= 2.31,P=0.025).On the other hand,the GSTP1 enzyme activities of cytoplasm in tumor cells with methylated status of GSTP1 gene were significantly lower than that in tumor cells with unmethylation (t=3.50,P=0.001).Conclusion GSTP1 inactivation via CpG island hypermethylation may contrib- ute to the pathogenesis of HCC.
6.Management of the multi-fracture of dental instruments in tooth root canal by microscope ultrasonic technique
Yong XIA ; Weixu CHEN ; Ping ZHANG ; Jiating LIN ; Qiuyan CHEN
Journal of Practical Stomatology 2014;(6):857-859
This paper summarizes 6 cases with multi-fracture of dental instruments in tooth root canal treated in our hospital from June 2011 to July 2013,the creation of a straight pathway,establishment of collateral bypass ,ultrasonic vibration,prevention of root perforation and secondary instrument fracture were emphasized,a reference in dealing with similar situations was provided.
7.Deficiency of TGF-?_1 in leukemic cells and the effects of exogenous TGF-?_1 gene on HL-60 cells
Yuanzhong CHEN ; Yong WU ; Ping CHEN ; Huifang HUANG
Chinese Journal of Pathophysiology 1986;0(01):-
AIM: To explore the existence of deficiency of TGF-?_1 in leukemia cells and its possible mechanism in the pathogenesis of leukemia. METHODS: The levels of TGF-?_1 were detected by ELISA in the cultured supernatant of leukemia cell lines and primary cells from patients with acute leukemia. TGF-?_1 gene was transduced into HL-60 cells by lipofectin-mediated DNA transfection. In the presence of G418, the HL-60 clone expressing TGF-?_1 was selected. The effects of exogenous TGF-?_1 gene on the proliferation and apoptosis of HL-60 cells were studied by leukemic colony assay, tumorigenicity in athymic nude mice, DNA fragmentation and cell cycle analysis. The expression of intrinsic TGF-?_1, [STBX]bcl-2 oncogene, hTERT mRNA on the apoptosis of HL-60 cells induced by exogenous TGF-?_1 gene were detected by RT-PCR. RESULTS: The levels of TGF-?_1 were obviously lower in the supernatant of leukemia cell lines and primary cells from patients with acute leukemia, as compared with normal controls (P
8. Application of precision medicine in rare neurodegenerative diseases
Journal of International Pharmaceutical Research 2017;44(2):145-150
Technological development has paved the way for accelerated genomic discovery and brought precision medicine into view. Genetics, bioinformatics, molecular imaging and management provide tools for realizing the idea of precision medicine. The goal of precision medicine is to deliver optimally targeted and timed interventions tailored to an individual’s molecular drivers of disease. It is very important for the implementation of precision medicine in rare neurodegenerative diseases, which are difficult to diagnose and treat. Precision medicine contributes to the identification of causative genes, the classification of genotypes and phenotypes of diseases, discovery of biomarkers with high sensitivity and specificity, and development of promising modified therapies. However, like the disadvantage encountered in other diseases, implementation of precision medicine in rare neurodegenerative diseases still confronts numerous challenges.
9.Clinical analysis of otogenic Mouret abscess: a case report.
Xin Ping HAO ; Biao CHEN ; Yong Xin LI
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2018;32(6):472-473
Mouret abscess is a rare extracranial complication of suppurative otitis media. It is generally believed to be a deep neck abscess caused by inflammation leading to the rupture of the bony tip of the mastoid tip. The location of Mouret abscess is deep. The symptoms are insidious at the onset, but may eventually spread to the surrounding tissue, and even lead to mediastinal abscess, cavernous sinus thrombosis, meningitis, dyspnea and other serious complications. At present, with the popularization of antibiotics, the occurrence rate of Mouret abscess is very low, and only sporadic cases have been reported.In this paper, a case of Mouret abscess caused by cholesteatoma was analyzed to explore Mouret abscess in terms of the route of infection, clinical manifestations, imaging features, diagnosis and treatment.
Abscess
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diagnosis
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drug therapy
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therapy
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Cholesteatoma
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complications
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Humans
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Mastoid
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pathology
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Meningitis
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Neck
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pathology
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Otitis Media
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Otitis Media, Suppurative
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complications