Pancreatic intraductal papillary mucinous neoplasm with sarcomatous transformation. A case report

Álvaro López-Janeiro , Ana Margarita Rodriguez , Marta Mendiola , Rula Nasimi Sabbagh , Jaime Feliu , Arantxa Villadóniga , Maria del Carmen Mendez
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Abstract

Mixed pancreatic epithelial and mesenchymal tumors are rare, usually invasive, entities. Intraductal papillary mucinous neoplasm (IPMN) is a precursor of invasive ductal carcinoma and shares mutations with its invasive counterparts. We report the case of a 72-year-old female with a previously undescribed sarcomatous transformation of a residual IPMN with no evidence of an invasive component. The mesenchymal component showed no heterologous differentiation. Both the epithelial and the mesenchymal populations showed aberrant expression of p53 protein and the same point mutation in KRAS gene. After a 6 month follow up, there were no signs of local or distant relapse. The present case suggests that sarcomatous transformation is possible in non-invasive, intraductal pancreatic lesions.

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胰腺导管内乳头状粘液瘤伴肉瘤转化。病例报告
胰腺上皮和间充质混合瘤是罕见的,通常是侵袭性实体瘤。导管内乳头状黏液性肿瘤(IPMN)是浸润性导管癌的前兆,与侵袭性导管癌有相同的突变。我们报告了一例72岁的女性,其先前未描述的残余IPMN的肉瘤转化,没有侵入性成分的证据。间充质成分未显示异源分化。上皮和间充质群体均表现出p53蛋白的异常表达和KRAS基因的同点突变。经过6个月的随访,没有出现局部或远处复发的迹象。目前的病例表明,在非侵入性胰腺导管内病变中,肉瘤转化是可能的。
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来源期刊
Revista Espanola de Patologia
Revista Espanola de Patologia Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
53
审稿时长
34 days
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