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一例成年男性胰腺实性假乳头状瘤透明细胞变异型病例。

A case of clear cell variant of solid-pseudopapillary tumor of the pancreas in an adult male patient.

机构信息

Laboratory of Cancer Research, Department of Pathology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.

出版信息

Ann Diagn Pathol. 2012 Apr;16(2):134-40. doi: 10.1016/j.anndiagpath.2010.11.011. Epub 2011 Mar 10.

DOI:10.1016/j.anndiagpath.2010.11.011
PMID:21396870
Abstract

A clear cell variant of solid-pseudopapillary tumor (SPT) of the pancreas was initially reported in 2006 as a tumor that arose in the pancreatic body and tail in young adults; to date, only 4 cases of this entity have been reported. Here, we present the case of a 58-year-old man with clear cell variant of SPT with distinctive clinicopathologic features. The tumor was well demarcated, was 2.6 cm in size and mostly composed of multivacuolated clear cells with solid growth, and exhibited the characteristic immunohistochemical positivity of β-catenin in the cytoplasm and nuclei of the neoplastic cells. In contrast to classical SPT with nuclear positivity, this case was negative for E-cadherin. Direct DNA sequencing of exon 3 of β-catenin gene demonstrated a single amino acid substitution (serine to phenylalanine) in codon 37, which is the phosphorylation site by GSKβ and frequently found in classical SPT. Electron microscopy demonstrated enlarged mitochondria and endoplasmic reticulum. Despite the fact that previous cases of clear cell variant of SPT arose mainly in the pancreatic body and tail in female young adults (age, 26-32 years), this case suggested that it is possible for a clear cell variant of SPT to arise in the pancreatic head in a middle-aged man. Because the recognition of the clear cell variant of SPT is important for the appropriate diagnosis of primary pancreatic tumor, the present case with its distinctive characteristics may provide new information for a more profound understanding of the pancreatic SPT.

摘要

胰腺实性假乳头状瘤(SPT)的透明细胞型于 2006 年首次报道,为发生于胰体尾部的青年肿瘤;截至目前,该肿瘤仅报道 4 例。本文报道 1 例 58 岁男性胰腺透明细胞型 SPT,具有独特的临床病理特征。肿瘤边界清楚,大小为 2.6cm,主要由多泡透明细胞构成实性生长,特征性免疫组化β-连环蛋白胞质和胞核阳性。与核阳性的经典 SPT 不同,本病例 E-钙黏蛋白阴性。β-连环蛋白基因外显子 3 的直接 DNA 测序显示,第 37 位密码子发生单个氨基酸取代(丝氨酸突变为苯丙氨酸),该位置是 GSKβ 的磷酸化位点,常见于经典 SPT。电镜显示扩大的线粒体和内质网。尽管之前报道的胰腺透明细胞型 SPT 主要发生于胰体尾部的年轻女性(年龄 26-32 岁),但本病例提示胰腺头部也可能发生中年男性胰腺透明细胞型 SPT。由于识别胰腺透明细胞型 SPT 对于原发性胰腺肿瘤的恰当诊断非常重要,本病例具有独特的特征,可能为更深入了解胰腺 SPT 提供新的信息。

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引用本文的文献

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Histol Histopathol. 2020 Mar;35(3):257-268. doi: 10.14670/HH-18-156. Epub 2019 Sep 3.
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Retrospective analysis of clinicopathological features of solid pseudopapillary neoplasm of the pancreas.胰腺实性假乳头状瘤临床病理特征的回顾性分析
Kaohsiung J Med Sci. 2016 Jul;32(7):356-61. doi: 10.1016/j.kjms.2016.05.009. Epub 2016 Jun 11.
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