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Duodenal neuroendocrine tumor-tertiary care centre experience:A case report
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作者 Uma Devi Malladi Suraj Kumar Chimata +4 位作者 Ramesh Kumar Bhashyakarla Sahitya Reddy Lingampally Vikas Reddy Venkannagari Zeeshan Ali Mohammed Rahul Vijay Vargiya 《World Journal of Translational Medicine》 2023年第1期1-8,共8页
BACKGROUND Neuroendocrine neoplasms(NENs)are a heterogeneous group of neoplasms arising from neuroendocrine cells,which contribute a small fraction of gastrointestinal malignancies.Duodenal neuroendocrine tumors(dNETs... BACKGROUND Neuroendocrine neoplasms(NENs)are a heterogeneous group of neoplasms arising from neuroendocrine cells,which contribute a small fraction of gastrointestinal malignancies.Duodenal neuroendocrine tumors(dNETs)represent 2%of all gastroenteropancreatic NENs.NENs are heterogeneous in terms of clinical symptoms,location,and prognosis.Non-functional NETs are mostly asymptomatic and need a high degree of clinical suspicion.Diagnosis of NETs is by endoscopic,endosonographic biopsy,and histopathological examination with immunohistochemistry staining for synaptophysin and chromogranin A.CASE SUMMARY We present case reports of 5 patients obtained over a period of 10 years in our center with dNETs.One patient had moderately differentiated NET and the remaining four had well-differentiated NET.Surveillance endoscopy was recommended in all the patients and is kept under regular follow-up after performing endoscopic therapy using endoscopic mucosal resection in 4 of them and one patient was advised to undergo a Whipple procedure.CONCLUSION Recently,the number of reported cases of NETs has increased due to advancements in diagnostic modalities and prevalence because of longer survival duration.The management differs based on the site,size,proliferation grade,and locally invasive pattern.They are slow-growing tumors with a good overall prognosis.The prognosis correlates with local lymph node status and metastasis. 展开更多
关键词 Chromogranin A Endoscopic mucosal resection-endoscopic submucosal resection Endoscopic submucosal dissection Ki-67 protein peptide receptor radionuclide Malladi UD et al.Duodenal neuroendocrine tumor
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Clinicopathological analysis of paraganglioma with literature review 被引量:6
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作者 Ning Feng Wen-Yan Zhang Xiao-Ting Wu 《World Journal of Gastroenterology》 SCIE CAS CSCD 2009年第24期3003-3008,共6页
AIM: To investigate the 152 cases of paragangliomas resected over the past 32 years in West China Hospital dinicopathologically.METHODS: All cases of paragangliomas diagnosed at the Department of Gastrointestinal Su... AIM: To investigate the 152 cases of paragangliomas resected over the past 32 years in West China Hospital dinicopathologically.METHODS: All cases of paragangliomas diagnosed at the Department of Gastrointestinal Surgery and Department of Pathology, West China Hospital, China were reviewed. The pathological documents were supplied by the Department of Pathology, West China Hospital, and other necessary data were extracted from the hospital records. The statistical analyses were performed by survival analysis (Kaplan-Meier method), descriptive statistical analyses and Х^2 analysis.RESULTS: The neuroendocrine marker vimentin was found to be selectively expressed in the benign tumors, and there were significant differences in the expression of those markers in both benign and malignant tumors. The survival analysis revealed that survival correlated significantly with the malignancy, metastasis and nodal status.CONCLUSION: Vimentin may be useful in the differential diagnosis between malignant and benign tumors. The difference in the expression of this marker in the tumors could be a clue to the future clinical diagnosis. The malignancy, metastasis and the nodal status may predict the prognosis of this disease. 展开更多
关键词 PARAGANGLIOMA Retroperitoneal tumor CARCINOMA neuroendocrine tumors neuroendocrine peptide VIMENTIN Survival analysis
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