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Variant anatomy of the biliary system as a cause of pancreatic and peri-ampullary cancers

  • Takashi Muraki
    ,
  • Michelle D. Reid
    ,
  • Burcin Pehlivanoglu
    ,
  • Raul S. Gonzalez
    ,
  • Aarti Sekhar
    ,
  • Bahar Memis
*Corresponding author for this work
  • Emory University
    ,
  • Beth Israel Deaconess Medical Center
    ,
  • Piedmont Hospital
    ,
  • Samsung Medical Center, Sungkyunkwan university
    ,
  • Medical College of Wisconsin
    ,
  • Koc University
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Background: The cause of most pancreatic and periampullary cancers (PAC) is unknown. Recently, anatomic variations such as pancreatobiliary maljunction have been recognized as risk factors, similar to Barrett-related gastro-esophageal cancers. Methods: Pre-operative MRI from 860 pancreatic/biliary resections, including 322 PACs, were evaluated for low-union (cystic duct joining the common hepatic duct inside of the pancreas or within 5 mm of the pancreatic border) Results: Low-union, seen <10% of the population, was present in 44% of PACs (73% distal bile duct/cholangiocarcinoma, 42% pancreatic head, and 34% ampullary). It was significantly lower(11%) in conditions without connection to the ductal system (thus not exposed to the ductal/biliary tract contents), namely mucinous cystic neoplasms and intrahepatic cholangiocarcinomas(p < 0.0001). Intra-pancreatic type low-union was seen in 16% of PACs versus 2% of controls(p < 0.0001). Discussion: This study establishes an association between low-union and PACs, and points to an anatomy-induced chemical/bilious carcinogenesis. This may explain why most pancreas cancers are in the head. It is possible that the same chemical milieu, caused by conditions other than low-union/insertion, may also play a role in the remaining half of PACs. This opens various treatment opportunities including milieu modifications (chemoprevention), focused screening of at-risk patients, and early detection with possible corrective actions.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1675-1685 (11 pages)

Journal (Volume, Issue Number)

HPB (Volume 22, Issue 12)

Publication milestones

  • Accepted/In press - 2020
  • Published - 12/2020

Publication status

Published - 12/2020

ISSN

1365-182X

Publication IDs

  • Scopus: 85083637358
  • PubMed: 32336556

Publication metrics

Metrics

SciVal
citations
2
SciVal
FWCI
0.59
SciVal
Author count
21
SciVal
Paper percentile
78
Fractional count
1
Fractional count
0.05
Fractional count
20
Fractional count
0.95
Fractional count
1
Fractional count
1
Scopus
citations

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