| Literature DB >> 30923792 |
Takanori Aota1, Shoji Kubo1, Shigekazu Takemura1, Shogo Tanaka1, Ryosuke Amano1, Kenjiro Kimura1, Sadaaki Yamazoe1, Hiroji Shinkawa1, Go Ohira1, Toshihiko Shibata1, Masaki Horiike2.
Abstract
AIM: Pancreaticobiliary maljunction (PBM) with or without congenital biliary dilatation (CBD) is a risk factor for biliary tract cancer. We investigated long-term outcomes after biliary diversion operation with special reference to types of CBD.Entities:
Keywords: biliary tract cancer; cholangitis; congenital biliary dilation; hepatolithiasis; pancreaticobiliary maljunction
Year: 2019 PMID: 30923792 PMCID: PMC6422791 DOI: 10.1002/ags3.12239
Source DB: PubMed Journal: Ann Gastroenterol Surg ISSN: 2475-0328
Characteristic of patients who underwent excision of the extrahepatic bile duct for pancreaticobiliary maljunction according to the type of congenital biliary dilatation
| Findings | Types |
| |
|---|---|---|---|
| Ia, Ic, no dilatation | IV‐A | ||
| (n = 20) | (n = 20) | ||
| Age | 46 (20‐73) | 44 (26‐67) | .880 |
| Gender (male:female) | 02:18 | 06:14 | .235 |
| Comorbidity | |||
| Biliary stone | 2 | 6 | .235 |
| Pancreatitis | 1 | 1 | >.999 |
| Congenital diseases | 1 (IDD) | 1 (Annular pancreas) | >.999 |
| I PMN | 0 | 1 | >.999 |
| Previous operation | |||
| Cholecystectomy (alone) | 1 | 0 | >.999 |
| Choledochoduodenostomy | 1 | 4 | .342 |
| Choledochojejunostomy | 0 | 1 | >.999 |
| Liver resection | 1 | 0 | >.999 |
| With hepatectomy | 1 | 4 | .342 |
IDD, intraductal duodenal diverticulum; IPMN, intraductal papillary mucinous neoplasm.
Type Ia (n = 9), Ic (n = 9), no dilatation (n = 2).
Posterior segmentectomy of the liver without excision of extrahepatic bile duct.
Characteristics of patients with biliary or pancreatic cancer after excision of extrahepatic bile duct for pancreaticobiliary maljunction
| Age/sex | Previous operation | Type of biliary dilatation | Duration between operation and cancer detection | Site of cancer | Treatment for cancer |
|---|---|---|---|---|---|
| 31/M | Choledocho‐duodenostomy | IV‐A | 24 y | Intrapancreatic BD | Pancreatoduodenectomy |
| 48/F | None | IV‐A | 3 y, 2 mo | Hilar BD | Chemotherapy |
| 67/F | None | IV‐A | 4 y, 1 mo | Intrahepatic BD | PTBD |
| 44/F | None | IV‐A | 5 y, 8 mo | Pancreas | Chemotherapy |
BD, bile duct; PTBD, percutaneous transhepatic biliary drainage.
Figure 1Cholangiocarcinoma and pancreatic cancer detected after the biliary diversion operation. A, Cholangiocarcinoma (arrow) is present around the residual bile duct in the pancreas. B, Space‐occupying lesion (hilar cholangiocarcinoma) is present (arrow). C, Space‐occupying lesion (intrahepatic cholangiocarcinoma) is present (arrow). D, Space‐occupying lesion (pancreatic cancer) is present (arrow)
Outcomes after excision of extrahepatic bile ducts according to the type of congenital biliary dilatation
| Outcomes | Types |
| |
|---|---|---|---|
| Ia, Ic, no dilatation(n = 20) | IV‐A(n = 20) | ||
| Repeated cholangitis | 1 | 8 | .0197 |
| Hepatolithiasis | 1 | 7 | .0436 |
| Death | 0 | 5 | .0471 |
| Cholangiocarcinoma | 0 | 3 | |
| Pancreatic cancer | 0 | 1 | |
| Hepatic failure | 0 | 1 | |
| Re‐operation | 0 | 5 | .0471 |
Figure 2Survival rates after the biliary diversion operation according to the types of congenital biliary dilatation. Group A comprised 20 patients classified as type Ia, Ic, or no dilation of the bile ducts, while group B comprised 20 patients classified as type IV‐A