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胰腺导管的鳞状样囊肿:胰腺中一种独特类型的囊性病变。

Squamoid cyst of pancreatic ducts: A distinct type of cystic lesion in the pancreas.

作者信息

Othman Mohammad, Basturk Olca, Groisman Gabe, Krasinskas Alyssa, Adsay N Volkan

机构信息

Department of Pathology, Wayne State University and Karmanos Cancer Institute, Detroit, MI 48021, USA.

出版信息

Am J Surg Pathol. 2007 Feb;31(2):291-7. doi: 10.1097/01.pas.0000213349.42143.ec.

Abstract

The clinicopathologic features of a hitherto unrecognized cystic tumor of the pancreas are documented, and its possible relationship to a more common incidental microscopic lesion is analyzed. Six patients (3 men and 3 women) had undergone resection specifically for this cyst type. The mean age of the patients was 63 years (range 52 to 79 y) and the mean size of the tumors was 2.6 cm (median 1.5, range 0.8 to 9 cm). The cysts had variable lining ranging from attenuated, flat squamoid cells to transitional, to stratified squamous without keratinization (no granular layer). The cells forming the basal/parabasal region expressed p63 (transitional/squamous cell marker, not detected in any normal pancreas or nonsquamous neoplasia) and the surface cells were positive for MUC 1 and MUC 6 (markers present in intercalated duct cells), and negative for GLUT-1 (consistent marker of serous adenomas). The lesions appeared to be unilocular cystic dilatation of the ducts that typically contained distinctive muco-proteinaceous acidophilic acinar secretions forming concretions, confirming their communication with the acinar system, and suggesting a localized obstruction in their pathogenesis (a form of "retention" cyst). A thin fibrous wall devoid of any lymphoid tissue separated the cysts from unremarkable parenchyma. There was no evidence of pancreatitis (fibrosis or inflammation). Separately, 110 pancreata resected for various reasons were analyzed, and what seems to be microscopic/incidental version of this process was identified in 10 examples (8%). These microcysts were found lying within compact acinar tissue, and appeared to be transforming from intercalated ducts, some focally connected to acinar elements, and they had abortive (nonbridging) septae with pseudo-loculated appearance, irregular contours and often showed tightly packed clusters of ducts with similar morphology described in the cases underwent resection specifically for this cyst type. In conclusion, the distinctive morphologic, immunophenotypic, and clinical characteristics of this cystic lesion warrant its classification as a separate entity. We propose to refer to it as squamoid cyst of pancreatic ducts. It seems to be a metaplastic cystic transformation beginning in the intercalated ducts. Although obstructive etiology is suspected, a specific factor or surrogate evidence of obstruction such as chronic pancreatitis is typically lacking.

摘要

本文记录了一种此前未被认识的胰腺囊性肿瘤的临床病理特征,并分析了其与一种更常见的偶然发现的微观病变的可能关系。6例患者(3男3女)因这种囊肿类型接受了切除术。患者的平均年龄为63岁(范围52至79岁),肿瘤的平均大小为2.6厘米(中位数1.5,范围0.8至9厘米)。囊肿的内衬细胞多样,从变薄的扁平鳞状细胞到移行细胞,再到无角化的复层鳞状细胞(无颗粒层)。形成基底/副基底区域的细胞表达p63(移行/鳞状细胞标志物,在任何正常胰腺或非鳞状肿瘤中均未检测到),表面细胞MUC 1和MUC 6呈阳性(闰管细胞中存在的标志物),而GLUT-1呈阴性(浆液性腺瘤的一致标志物)。病变表现为导管的单房囊性扩张,通常含有独特的黏液蛋白嗜酸性腺泡分泌物形成的结石,证实其与腺泡系统相通,并提示其发病机制中存在局部梗阻(一种“潴留”囊肿形式)。一层无任何淋巴组织的薄纤维壁将囊肿与正常实质分隔开。没有胰腺炎(纤维化或炎症)的证据。另外,对因各种原因切除的110个胰腺进行了分析,在10个样本(8%)中发现了似乎是该过程的微观/偶然版本。这些微囊肿位于致密的腺泡组织内,似乎是从闰管转变而来,一些局部与腺泡成分相连,它们有发育不全(不相连)的间隔,呈假分叶状外观,轮廓不规则,并且经常显示出紧密排列的形态相似的导管簇,与专门针对这种囊肿类型进行切除的病例中描述的情况相似。总之,这种囊性病变独特的形态学、免疫表型和临床特征使其有理由被分类为一个独立的实体。我们建议将其称为胰腺导管鳞状囊肿。它似乎是一种起源于闰管的化生囊性转变。尽管怀疑有梗阻性病因,但通常缺乏诸如慢性胰腺炎等梗阻的特定因素或替代证据。

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