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首页> 外文期刊>Human Pathology >Mucinous nonneoplastic cyst of the pancreas: apomucin phenotype distinguishes this entity from intraductal papillary mucinous neoplasm.
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Mucinous nonneoplastic cyst of the pancreas: apomucin phenotype distinguishes this entity from intraductal papillary mucinous neoplasm.

机译:胰腺粘液性非肿瘤性囊肿:阿朴粘蛋白表型将此实体与导管内乳头状粘液性肿瘤区分开。

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摘要

Mucinous nonneoplastic cyst of the pancreas is a newly described and rare cystic lesion with unknown histogenesis. It is defined as a cystic lesion lined with mucinous epithelium, supported by hypocellular stroma and not communicating with the pancreatic ducts. It is very challenging to differentiate this lesion from other cystic mucinous neoplasms of the pancreas such as branch-duct intraductal papillary mucinous neoplasm by morphology. In this study, a total of 436 pancreatic specimens resected between 2002 and 2007 in our institution were reviewed. Fifteen (3.4%, 15/436) mucinous nonneoplastic cysts were identified. They included 3 males and 12 females, with a median age of 60 years. Forty-six percent of cases (7/15) occurred in pancreatic head, 27% (4/15) in neck, 7% (1/15) in body, and 20% (3/15) in tail. The size of lesions ranged from 0.5 to 3.5 cm in greatest dimension. In most cases (12/15, 80%), mucinous nonneoplastic cyst was associated or adjacent to acinar-ductal mucinous metaplasia. These morphologic data indicate that mucinous nonneoplastic cyst is not really a rare disease and may originate from acinar-duct mucinous metaplasia histogenestically. Furthermore, apomucin immunostains of mucinous nonneoplastic cyst showed MUC1 expressed in 27% (4/15) cases, MUC5AC in 67% (10/15 cases), and MUC2 was were negative in all cases, whereas intraductal papillary mucinous neoplasm (n = 17; 5 main duct type, 12 branch-duct type) showed focal and weak MUC1 positivity in 18% (3/17) cases, MUC2 positivity in 71% (12/17) cases, and all intraductal papillary mucinous neoplasm (17/17) were MUC5AC positive. The clonality assay with the HUMARA gene revealed that the mucinous nonneoplastic cysts were of polyclonal origin. For the first time, using HUMARA assay, we demonstrate the nonneoplastic nature of these cysts and further characterize morphologic and immunophenotypic properties that allow differentiation from intraductal papillary mucinous neooplasm.
机译:胰腺粘液性非肿瘤性囊肿是一种新近描述的罕见组织病性囊性病变。它被定义为衬有粘液上皮的囊性病变,由细胞下层基质支持,不与胰管连通。通过形态学将该病灶与胰腺的其他囊性粘液性肿瘤如分支导管导管内乳头状粘液性肿瘤区分开来是非常具有挑战性的。在本研究中,我们对2002年至2007年间切除的436个胰腺标本进行了回顾。鉴定出十五个(3.4%,15/436)粘液性非肿瘤性囊肿。他们包括3名男性和12名女性,平均年龄为60岁。 46%(7/15)的病例发生在胰头,27%(4/15)的颈部,7%(1/15)的身体和20%(3/15)的尾巴。病变的最大尺寸在0.5至3.5厘米之间。在大多数情况下(12 / 15,80%),粘液性非肿瘤性囊肿与腺泡导管粘液化生相关或相邻。这些形态学数据表明,粘液性非肿瘤性囊肿并不是真正罕见的疾病,可能是组织学上起源于腺泡管粘液化生。此外,黏液性非肿瘤性囊肿的载脂蛋白免疫染色显示,MUC1在27%(4/15)的病例中表达,MUC5AC在67%(10/15的病例)中表达,而MUC2在所有病例中均为阴性,而导管内乳头状黏液性肿瘤(n = 17) ; 5个主导管型,12个分支导管型)表现为局灶性MUC1阳性和弱MUC1阳性(3/17)例,MUC2阳性71%(12/17)例,所有导管内乳头状黏液性肿瘤(17/17) )为MUC5AC阳性。 HUMARA基因的克隆性分析表明,粘液性非肿瘤性囊肿是多克隆来源的。第一次,使用HUMARA分析,我们证明了这些囊肿的非肿瘤性质,并进一步表征了形态学和免疫表型特性,可以从导管内乳头状黏液性肿瘤中分化出来。

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