Chang Xiao-yan, Lu Zhao-hui, Li Xing-qi, Chen Jie
Department of Pathology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Science, Beijing 100730, China.
Zhonghua Bing Li Xue Za Zhi. 2013 Apr;42(4):248-51. doi: 10.3760/cma.j.issn.0529-5807.2013.04.008.
To study the pathologic features, diagnosis, differential diagnosis and molecular characteristics of intraductal tubulopapillary neoplasm of the pancreas (ITPN).
The clinical findings, morphologic features, immunophenotype (by EnVision method) and KRAS gene alterations (by reverse transcriptase-polymerase chain reaction) of 6 cases of ITPN encountered during the period from January, 2001 to June, 2010 were analyzed.
There were altogether 2 males and 4 females. The mean age of the patients was 64 years. Gross examination showed that the tumors were located in large pancreatic ducts and appeared as polypoid nodules with ductal obstruction. Solid tumor nodules associated with adjoining dilated ducts were identified in one case. Histologically, the tumors were characterized by tubulopapillary growth pattern without luminal mucin. The tumor cells showed high-grade nuclear atypia with scanty intracytoplasmic mucin. Intraductal necrotic foci were frequently observed. Immunohistochemical study showed that the tumor cells expressed CK7 and CK19. Focal positivity for MUC5AC was demonstrated. Two cases expressed MUC1. The staining for MUC2 was negative. KRAS gene mutations were identified in 2 cases, with a single-amino-acid substitution in codon 12 (35G > A and 35G > T/34G > A).
ITPN is a newly described pancreatic intraductal neoplasm and different from intraductal papillary mucinous neoplasm. ITPN is characterized by intraductal tubulopapillary growth pattern, severe cytologic atypia and scanty mucin secretion.
研究胰腺导管内管状乳头状肿瘤(ITPN)的病理特征、诊断、鉴别诊断及分子特征。
分析2001年1月至2010年6月间遇到的6例ITPN的临床资料、形态学特征、免疫表型(采用EnVision法)及KRAS基因改变(采用逆转录聚合酶链反应)。
6例患者中男性2例,女性4例。患者平均年龄64岁。大体检查显示肿瘤位于胰腺大导管内,呈息肉样结节伴导管阻塞。1例可见与相邻扩张导管相关的实性肿瘤结节。组织学上,肿瘤以无管腔内黏液的管状乳头状生长模式为特征。肿瘤细胞显示高级别核异型性,胞质内黏液稀少。导管内坏死灶常见。免疫组织化学研究显示肿瘤细胞表达CK7和CK19。MUC5AC呈局灶阳性。2例表达MUC1。MUC2染色阴性。2例检测到KRAS基因突变,密码子12发生单氨基酸替换(35G>A和35G>T/34G>A)。
ITPN是一种新描述的胰腺导管内肿瘤,与导管内乳头状黏液性肿瘤不同。ITPN的特征为导管内管状乳头状生长模式、严重的细胞学异型性及黏液分泌稀少。