pancreas divisum
Recently Published Documents


TOTAL DOCUMENTS

626
(FIVE YEARS 65)

H-INDEX

41
(FIVE YEARS 3)

2021 ◽  
Vol 8 (4) ◽  
Author(s):  
Gennaro CASABURO ◽  
Marcella CERRATO ◽  
Giovanna B. FIERRO ◽  
Gaetano CIMMINO ◽  
Giuseppe PANASCÌ

2021 ◽  
pp. 1579-1594
Author(s):  
Alberto Mariani ◽  
Sabrina Testoni ◽  
Paolo Giorgio Arcidiacono

2021 ◽  
Vol 9 ◽  
Author(s):  
Guixian Pan ◽  
Kaihua Yang ◽  
Biao Gong ◽  
Zhaohui Deng

Background: Endoscopic retrograde cholangiopancreatography (ERCP) has been increasingly performed in children with symptomatic pancreas divisum (PD).Aim: To investigate the safety and efficacy of ERCP in the treatment of children with symptomatic PD.Methods: We performed a retrospective analysis on children with PD who were treated with ERCP at Shanghai Children's Medical Center between June 2015 and May 2020. Pertinent patient, clinical and procedural data were collected to assess the therapeutic effects and identify the risk factors for post-ERCP pancreatitis (PEP).Results: Overall, 114 ERCPs were performed in 46 children with PD. With a median follow-up of 28.5 months (12–71 months), 40 (87.0%) children achieved clinical remission, the median number of acute pancreatitis episodes decreased from four times per year pre-operatively to once per year post-operatively (P < 0.001), and the nutritional score improved post-operatively (P = 0.004). The incidence of PEP was 7.9%, and female sex, stone extraction, and gene mutations were identified as possible risk factors for PEP on univariate analysis. However, there was no statistical significance on multivariate analysis (P > 0.05).Conclusion: Therapeutic ERCP is an effective and safe intervention for children with symptomatic PD.


2021 ◽  
Vol 49 (11) ◽  
pp. 030006052110601
Author(s):  
Kunyi Liu ◽  
Xuechen Liu ◽  
Chengyi Shi ◽  
Siqi Liu ◽  
Hongwei Du ◽  
...  

Pancreas divisum (PD) is a common pancreatic malformation caused by the failure of fusion between ventral and dorsal pancreatic ducts. There is a small branch of communication between the two systems in incomplete PD, and this variation has an incidence of 15%. A 43-year-old female patient presented to our department with recurrent abdominal pain. Magnetic resonance cholangiopancreatography (MRCP) showed that the ventral pancreatic duct was curved, with a local pouchlike dilatation. Endoscopic ultrasonography supported the diagnosis of incomplete PD and showed a thin branch of communication between ventral and dorsal pancreatic ducts. Endoscopic retrograde cholangiopancreatography (ERCP) and papillotomy of the minor papilla with double plastic stent implantation were performed. One pancreatic plastic stent was inserted across the minor and major papilla over the guide wire, creating a U-shape. The other wire-guided plastic stent was inserted through the minor papilla into the dorsal pancreatic duct. The pancreatic fluid drained smoothly after stent placement. During the 6-month follow-up, the patient remained well, without recurrence of pancreatitis.


DEN Open ◽  
2021 ◽  
Vol 2 (1) ◽  
Author(s):  
Shinya Kawaguchi ◽  
Tatsunori Satoh ◽  
Shuzo Terada ◽  
Shinya Endo ◽  
Naofumi Shirane

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Naoto Takahashi ◽  
Hiroyuki Nitta ◽  
Akira Umemura ◽  
Hirokatsu Katagiri ◽  
Shoji Kanno ◽  
...  

Abstract Background The complication of duplication of alimentary tracts and pancreas divisum (PD) is a rare malformation and the development of pancreatic ductal adenocarcinoma (PDAC) in this malformation is also extremely rare. There have been some reports of complication of malignancy in a gastric duplication cyst (GDC) and PD. However, there have been no reports of complication of PDAC in cases with GDC and PD. Case presentation A 54-year-old woman was followed up at the previous hospital due to a history of ovarian endometrial adenocarcinoma. She also had a surgical history of partial excision for a GDC and pancreatic tail of PD in her childhood. A gynecological follow-up computed tomography (CT) examination revealed the pancreatic body tumor and the bifurcated main pancreatic duct dilatation. Furthermore, magnetic resonance cholangiopancreatography also revealed that the ventral main pancreatic duct communicated with the GDC. The initial levels of tumor markers were high, but we could not achieve preoperative histopathological diagnosis. The preoperative diagnosis was PDAC occurring in a case with PD and GDC. She received two courses of neoadjuvant chemotherapy with gemcitabine and nab-paclitaxel. A CT examination after neoadjuvant chemotherapy revealed the shrinkage of the tumor, and then we performed distal pancreatectomy with splenectomy and GDC resection. A histopathological examination revealed invasive PDAC and lymph node metastases; pathological staging was T1N1M0, stage III. Furthermore, PD and GDC were also histopathologically detected. The postoperative course was uneventful, and she was discharged on the postoperative day 25. She received S-1 monotherapy for 6 months, and no recurrence has been detected at 1 year after radical resection. Conclusions We herein presented an extremely rare combined case of PD, GDC and PDAC. We successfully treated it by neoadjuvant chemotherapy and distal pancreatectomy with GDC resection, and postoperative chemotherapy.


2021 ◽  
Vol 2 (12) ◽  
pp. 48-55
Author(s):  
Eduardo Salloum Filho ◽  
Rafael Portella Almeida Grattapaglia ◽  
Luana Dantas Barbosa ◽  
Liliana Sampaio Costa Mendes

Introdução: Pancreas Divisum é uma anomalia anatômica do ducto pancreático em que a maioria do suco pancreático passa pela papila menor e a minoria pela papila maior. Relato de caso: Paciente com 54 anos com Pâncreas Divisumque obteve diagnóstico de pâncreas divisum ocasionalmente durante investigação para elucidação de enzimas hepáticas alteradas e dispepsia. Discussão: Pâncreas Divisum é uma entidade pouco abordada devido à falta de sintomatologia na maioria dos casos, mas há indícios mais recentes que apontam que essa entidade poderia estar relacionada com a maior incidência de outras patologias como pancreatites e tumor pancreático. Conclusão: Por ser uma doença rara e assintomática e, pela possibilidade de evoluir com complicações, deve-se pensar preemptivamente no intuito de prever diagnósticos mais precoces para que se possa intervir em casos de necessidade e evitar desfechos desfavoráveis.


Sign in / Sign up

Export Citation Format

Share Document