作者: W. Meyer , J. Köhler , C. Gebhardt
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摘要: Introduction: Among the rare cystic pancreatic tumors, serous and mucinous cystadenoma cystadenocarcinoma are most often diagnosed. Case: We report on a total of 21 patients with neoplasms who underwent surgery, 11 whom had cystadenocarcinoma. Of 10 remaining patients, were diagnosed in two groups five. A common feature all is slow growth, leading to clinical symptoms at an advanced stage, tumors frequently becoming enormous. Results: In approximately half cases, diagnosis was possible by means ultrasound, computed tomography and, three instances, preoperative percutaneous aspiration. Differential pseudocysts proved be difficult. Conclusion: Given low operative risk, resection should always performed instances where findings cannot clearly identified. Moreover, compared ductal carcinomas, prognosis after early extremely favorable, so that postponing might reduce patient's prospects being cured.