Intracholecystic Papillary Neoplasms Are Distinct From Papillary Gallbladder Cancers A Clinicopathologic and Exome-sequencing Study

被引:37
作者
Akita, Masayuki [1 ,2 ]
Fujikura, Kohei [1 ]
Ajiki, Tetsuo [2 ]
Fukumoto, Takumi [2 ]
Otani, Kyoko [1 ]
Hirose, Takanori [3 ]
Tominaga, Masahiro [4 ]
Itoh, Tomoo [1 ]
Zen, Yoh [1 ,5 ]
机构
[1] Kobe Univ, Grad Sch Med, Dept Diagnost Pathol, Kobe, Hyogo, Japan
[2] Kobe Univ, Grad Sch Med, Dept Hepatobiliary Pancreat Surg, Kobe, Hyogo, Japan
[3] Hyogo Canc Ctr, Dept Pathol, Akashi, Hyogo, Japan
[4] Hyogo Canc Ctr, Dept Gastroenterol Surg, Akashi, Hyogo, Japan
[5] Kings Coll Hosp London, Inst Liver Studies, London SE5 9RS, England
关键词
mucus; intraductal papillary neoplasm; STK11; APC; PEUTZ-JEGHERS-SYNDROME; BILIARY-TRACT; MUTATIONS; CARCINOMA; ADENOMAS; POLYPS;
D O I
10.1097/PAS.0000000000001237
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Although intracholecystic papillary neoplasms (ICPNs) have been increasingly recognized, their features remain unclear because of the lack of standardized definition. This study aimed to elucidate clinicopathologic and genetic features of ICPNs using stringent diagnostic criteria. On the basis of the recently proposed criteria, gallbladder neoplasms showing delicate papillary growth were diagnosed as ICPNs, while polypoid papillary adenocarcinomas arranged in a complex architecture were categorized as papillary gallbladder cancers (GBCs). Clinicopathologic features were compared among ICPNs (n= 7), papillary GBCs (n= 24), and nonpapillary GBCs (n= 44). Whole-exome and validation Sanger sequencing was also conducted. Gross mucin hypersecretion was detected in 3/7 ICPNs (43%), 1/24 papillary GBCs (4%), and 1/44 nonpapillary GBCs (2%) (P< 0.001). All patients with ICPN lacked lymphovascular invasion and nodal metastasis, while these features were occasionally observed in patients with papillary or nonpapillary GBC (13% to 59%). ICPNs were less advanced than papillary and nonpapillary GBCs (P< 0.001) with all cases of ICPNs being recurrence-free. Whole-exome and Sanger sequencing identified somatic mutations in STK11 (a causative gene of Peutz-Jegher syndrome; n= 3), CTNNB1 (n= 2), and APC (a gene of familial adenomatous polyposis; n= 1) in ICPNs, while those alterations were exceptional in papillary and nonpapillary GBCs. ICPNs more commonly showed cytoplasmic and/or nuclear expressions of ss-catenin than papillary and nonpapillary GBCs. In conclusion, the histologybased classification of gallbladder papillary neoplasms is useful for identifying ICPNs that share clinicopathologic features with the pancreatic counterpart. ICPNs meeting the criteria were genetically distinct from papillary and nonpapillary GBCs, with STK11, CTNNB1, and APC being identified as major driver genes for ICPNs.
引用
收藏
页码:783 / 791
页数:9
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