Intraductal papillary neoplasm of the bile duct (IPN-B): also a disease of western Caucasian patients. A literature review and case series

2016 ◽  
Vol 71 (1) ◽  
pp. e79-e87 ◽  
Author(s):  
D. Mondal ◽  
M.A. Silva ◽  
Z. Soonawalla ◽  
L.M. Wang ◽  
H.K. Bungay
HPB ◽  
2021 ◽  
Vol 23 ◽  
pp. S935-S936
Author(s):  
J.M. Ramia ◽  
M. Serradilla-Martin ◽  
P. Melgar-Requena ◽  
S. Paterna-Lopez ◽  
C. Villodre ◽  
...  

2018 ◽  
Vol 50 (3) ◽  
pp. 578-582 ◽  
Author(s):  
Ignacio Fuente ◽  
Marcos Gonzalez ◽  
Martin de Santibañes ◽  
Juan Pekolj ◽  
Oscar Mazza ◽  
...  

2019 ◽  
Vol 6 (7) ◽  
pp. 2579
Author(s):  
Nuray Colapkulu ◽  
Gurhan Bas ◽  
Fatih Buyuker ◽  
Damla Beyazadam ◽  
Ibrahim A. Ozemir ◽  
...  

A 67 year old male with right upper quadrant abdominal pain diagnosed with intraductal papillary neoplasm of bile ducts (IPNB) by endoscopic biopsy. The patient was treated surgically and disease free on first year follow-up. Intraductal papillary neoplasm of bile duct (IPNB) is a rare entity with malignant counterparts and recently classified by The World Health Organization. The aim of this study is to present a case of IPNB and review the literature. Pubmed/MEDLINE was searched and articles were extracted. Twenty four case reports and 17 retrospective case series were evaluated. From 41 studies, 824 cases were included. There was slight male predominancy among patients and almost all cases were from eastern countries. Even though the etiology remains unclear, hepatolithiasis was the most common potential etiological association. Most cases were treated with surgical intervention. More than half of the 577 resected specimens had invasive component. Incidence rate of histopathological subtypes were as fallowed: Intestinal (35%), pancreaticobiliary (32%), gastric (19%) and oncocytic (12%). Intraductal papillary neoplasm of bile duct has an increased malignancy rates at postoperative pathological diagnosis, consequently early surgical management is important.


2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Rumi Matono ◽  
Mizuki Ninomiya ◽  
Kazutoyo Morita ◽  
Takahiro Tomino ◽  
Yumi Oshiro ◽  
...  

2015 ◽  
Vol 100 (11-12) ◽  
pp. 1443-1448
Author(s):  
Norio Kubo ◽  
Hideki Suzuki ◽  
Norihiro Ishii ◽  
Mariko Tsukagoshi ◽  
Akira Watanabe ◽  
...  

Duodenum mucinous carcinoma is very rare, and the prognosis of the patient is very bad, especially when the tumor is invasive to other organs. In this case, duodenum carcinoma was invasive to common bile duct and transverse colon. Mucinous fluid, which was secreted from a duodenum tumor, was found in the dilatated bile duct. The intraductal papillary neoplasm of the bile duct was considered a differential diagnosis. We performed aggressive resection and had a good prognosis. A 74-year-old woman received a diagnosis of cholangitis and was treated with antibiotic drugs. Endoscopic retrograde cholangiopancreatography revealed a defect in the lower common bile duct with the mucoid fluid. We suspected intraductal papillary neoplasm of the bile duct, but no malignant cells were detected. One year later, gastrointestinal fiberscopy revealed a villous tumor in the postbulbar portion of the duodenum; adenocarcinoma was detected in biopsy specimens. Computed tomography revealed dilatation of the duodenum with an enhanced tumor, and dilatation of both the common and intrahepatic bile ducts. Magnetic resonance cholangiopancreatography revealed that the duodenum was connected with the common bile duct and ascending colon. We resected the segmental duodenum, extrahepatic bile duct, left lobe of liver, a partial of the transverse colon, and associated lymph nodes. Although the advanced duodenal carcinoma had poor prognosis, the patient was alive, without recurrence, 5 years after the operation.


2013 ◽  
Vol 1 (6) ◽  
pp. 965-969 ◽  
Author(s):  
MITSURU FUJITA ◽  
NORITAKA WAKUI ◽  
YOSHIYA YAMAUCHI ◽  
YUKI TAKEDA ◽  
TAKEMASA SATO ◽  
...  

2008 ◽  
Vol 453 (6) ◽  
pp. 589-598 ◽  
Author(s):  
Kee-Taek Jang ◽  
Seung-Mo Hong ◽  
Kyu Taek Lee ◽  
Jong Gyun Lee ◽  
Seoung Ho Choi ◽  
...  

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