Department of Pathology, Mount Sinai School of Medicine, One Gustave L Levy Place, 1194, New York, NY 10029, USA.
Endocr Pathol. 2013 Mar;24(1):30-5. doi: 10.1007/s12022-012-9231-x.
Pancreatic neuroendocrine tumors of the main pancreatic duct are rare and usually small due to symptoms of pancreatic duct obstruction. We present a case of a large (3 cm), well-differentiated (G1) lipid-rich polypoid neuroendocrine tumor of the pancreas completely occluding the main pancreatic duct with non-neoplastic-entrapped ductules and CK19 positivity. Clinical, radiological, gross, microscopic, immunohistochemical, and ultrastructural findings are discussed. The literature pertaining to the unique features of this case is reviewed including clinical and pathologic pitfalls and the possible etiologic and prognostic significance of these findings.
胰腺主胰管内神经内分泌肿瘤罕见,且由于胰管阻塞的症状通常较小。我们报告了一例大(3 厘米)、分化良好(G1)、富含脂质的息肉样胰腺神经内分泌肿瘤,该肿瘤完全阻塞主胰管,伴有非肿瘤性包裹的小管和 CK19 阳性。讨论了临床、放射学、大体、显微镜下、免疫组织化学和超微结构表现。回顾了与该病例独特特征相关的文献,包括临床和病理陷阱,以及这些发现的可能病因和预后意义。