Department of Pathology, Tokai University School of Medicine, Isehara 259-1193, Japan.
World J Gastroenterol. 2013 Jun 7;19(21):3358-63. doi: 10.3748/wjg.v19.i21.3358.
Solid pseudopapillary neoplasm (SPN) is a rare and low-grade malignant pancreatic neoplasm composed of poorly cohesive monomorphic neoplastic cells forming solid and pseudopapillary structures with frequent hemorrhagic-cystic degeneration. Intraductal papillary mucinous neoplasm (IPMN) is a pancreatic exocrine tumor composed of intraductal papillary growth of mucin containing neoplastic cells in the main pancreatic duct or its major branches. In the case presented here, a 53-year-old, Japanese man was found to have multiple cystic lesions and dilatation of the main pancreatic duct in the neck of the pancreas. Histological examination revealed a main-duct and branch-duct type IPMN, of the gastric-type, involving the neck of the pancreas, associated with a 0.5 cm SPN in the caudal side of the IPMN. We diagnosed this case as synchronous SPN and IPMN. As far as we know, only one other case of synchronous SPN and IPMN has been reported. Both the present case and the previously reported case showed abnormal nuclear expression of β-catenin in SPN, whereas IPMN showed no abnormal nuclear expression. These results suggest that β-catenin abnormality is not a common pathogenetic factor of synchronous SPN and IPMN.
实性假乳头状瘤(SPN)是一种罕见的低度恶性胰腺肿瘤,由缺乏黏附性的单形性肿瘤细胞组成,形成实性和假乳头状结构,常伴有出血囊性变性。导管内乳头状黏液性肿瘤(IPMN)是一种胰腺外分泌肿瘤,由主胰管或其主要分支内的黏蛋白分泌性肿瘤细胞的导管内乳头状生长构成。在此例中,一名 53 岁的日本男性被发现胰腺颈部有多个囊性病变和主胰管扩张。组织学检查显示主胰管和分支胰管型 IPMN,胃型,累及胰腺颈部,与 IPMN 尾侧的 0.5 cm SPN 相关。我们诊断该病例为同步 SPN 和 IPMN。据我们所知,仅有一例同步 SPN 和 IPMN 的病例报告。本病例和先前报道的病例均显示 SPN 中β-连环蛋白的异常核表达,而 IPMN 中无异常核表达。这些结果表明β-连环蛋白异常不是同步 SPN 和 IPMN 的共同发病因素。