Management of the late effects of disconnected pancreatic duct syndrome: A case report.

Case report Disconnected pancreatic duct syndrome Endoscopy Necrosis Pancreas Walled-off necrosis

Journal

World journal of clinical cases
ISSN: 2307-8960
Titre abrégé: World J Clin Cases
Pays: United States
ID NLM: 101618806

Informations de publication

Date de publication:
06 May 2019
Historique:
received: 18 01 2019
revised: 06 03 2019
accepted: 26 03 2019
entrez: 25 5 2019
pubmed: 28 5 2019
medline: 28 5 2019
Statut: ppublish

Résumé

There have been few reports about the late effects of disconnected pancreatic duct syndrome (DPDS). Although few reports have described the recurrence interval of pancreatitis, it might be rare for recurrence to occur more than 5 years later. Herein, we describe a case of recurrence in an 81-year-old man after the treatment of walled-off necrosis (WON) with pancreatic transection 7 years ago. An 81-year-old man visited our hospital with chief complaints of fever and abdominal pain 7 years after the onset of WON due to severe necrotic pancreatitis. His medical history included an abdominal aortic aneurysm (AAA), hypertension, dyslipidemia, and chronic kidney disease. Computed tomography (CT) scan showed that the pancreatic fluid collection (PFC) had spread to the aorta with inflammation surrounding it, and CT findings suggested that bleeding occurred from the vasodilation due to splenic vein occlusion. First, we attempted to perform transpapillary drainage because of venous dilation around the residual stomach and the PFC. However, pancreatic duct drainage failed because of complete main pancreatic duct disruption. Second, we performed endoscopic ultrasound-guided drainage. After transmural drainage, the inflammation improved and stenting for the AAA was performed successfully. The inflammation was resolved, and he has been free from infection for more than 2 years after the procedure. This case highlights the importance of continued follow-up of patients for recurrence after the treatment of WON with pancreatic transection.

Sections du résumé

BACKGROUND BACKGROUND
There have been few reports about the late effects of disconnected pancreatic duct syndrome (DPDS). Although few reports have described the recurrence interval of pancreatitis, it might be rare for recurrence to occur more than 5 years later. Herein, we describe a case of recurrence in an 81-year-old man after the treatment of walled-off necrosis (WON) with pancreatic transection 7 years ago.
CASE SUMMARY METHODS
An 81-year-old man visited our hospital with chief complaints of fever and abdominal pain 7 years after the onset of WON due to severe necrotic pancreatitis. His medical history included an abdominal aortic aneurysm (AAA), hypertension, dyslipidemia, and chronic kidney disease. Computed tomography (CT) scan showed that the pancreatic fluid collection (PFC) had spread to the aorta with inflammation surrounding it, and CT findings suggested that bleeding occurred from the vasodilation due to splenic vein occlusion. First, we attempted to perform transpapillary drainage because of venous dilation around the residual stomach and the PFC. However, pancreatic duct drainage failed because of complete main pancreatic duct disruption. Second, we performed endoscopic ultrasound-guided drainage. After transmural drainage, the inflammation improved and stenting for the AAA was performed successfully. The inflammation was resolved, and he has been free from infection for more than 2 years after the procedure.
CONCLUSION CONCLUSIONS
This case highlights the importance of continued follow-up of patients for recurrence after the treatment of WON with pancreatic transection.

Identifiants

pubmed: 31123678
doi: 10.12998/wjcc.v7.i9.1053
pmc: PMC6511923
doi:

Types de publication

Case Reports

Langues

eng

Pagination

1053-1059

Déclaration de conflit d'intérêts

Conflict-of-interest statement: The authors declare that they have no conflict of interest.

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Auteurs

Reiko Yamada (R)

Department of Gastroenterology and Hepatology, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan. reiko-t@clin.medic.mie-u.ac.jp.

Yuhei Umeda (Y)

Department of Gastroenterology and Hepatology, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.

Yasunori Shiono (Y)

Department of Gastroenterology and Hepatology, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.

Hiroaki Okuse (H)

Department of Gastroenterology and Hepatology, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.

Naoki Kuroda (N)

Department of Gastroenterology and Hepatology, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.

Junya Tsuboi (J)

Department of Endoscopy, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.

Hiroyuki Inoue (H)

Department of Gastroenterology and Hepatology, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.

Yasuhiko Hamada (Y)

Department of Endoscopy, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.

Kyosuke Tanaka (K)

Department of Endoscopy, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.

Noriyuki Horiki (N)

Department of Endoscopy, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.

Yoshiyuki Takei (Y)

Department of Gastroenterology and Hepatology, Mie University Graduate School of Medicine, Tsu, Mie 514-8507, Japan.

Classifications MeSH