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A successfully treated case of Lemmel syndrome with pancreaticobiliary maljunction: A case report
BACKGROUND: Lemmel syndrome is a rare condition that leads to cholangitis and/or pancreatitis due to intraduodenal diverticulum. Surgery is considered for the treatment of severe or repeated symptoms in patients with this condition. CASE PRESENTATION: An 81-year-old woman was admitted to our hospita...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327874/ https://www.ncbi.nlm.nih.gov/pubmed/32698288 http://dx.doi.org/10.1016/j.ijscr.2020.06.080 |
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author | Yanagaki, Mitsuru Shiba, Hiroaki Hagiwara, Shin Hoshino, Masato Sakuda, Hitoshi Furukawa, Yoshiyuki Yanaga, Katsuhiko |
author_facet | Yanagaki, Mitsuru Shiba, Hiroaki Hagiwara, Shin Hoshino, Masato Sakuda, Hitoshi Furukawa, Yoshiyuki Yanaga, Katsuhiko |
author_sort | Yanagaki, Mitsuru |
collection | PubMed |
description | BACKGROUND: Lemmel syndrome is a rare condition that leads to cholangitis and/or pancreatitis due to intraduodenal diverticulum. Surgery is considered for the treatment of severe or repeated symptoms in patients with this condition. CASE PRESENTATION: An 81-year-old woman was admitted to our hospital, complaining of general fatigue, BT 38.8 degree, and right hypochondoralgia. Her hepatobiliary enzyme levels were elevated, and enhanced abdominal computed tomography revealed dilation of the common bile duct and intraduodenal diverticulum. After restarting oral intake, her symptoms were exacerbated. Endoscopic retrograde cholangio-pancreatography (ERCP) revealed pancreaticobiliary maljunction and parapapillary diverticulum. Under a diagnosis of Lemmel syndrome with pancreaticobiliary maljunction complicated by acute pancreatitis and cholangitis, we performed extrahepatic bile duct resection with cholecystectomy and papilloplasty. Her postoperative course was uneventful, and the patient was discharged 20 days after surgery. She remains well at 5 months after surgery. CONCLUSION: We herein report a successfully diagnosed and treated case of Lemmel syndrome with pancreaticobiliary maljunction. |
format | Online Article Text |
id | pubmed-7327874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-73278742020-07-06 A successfully treated case of Lemmel syndrome with pancreaticobiliary maljunction: A case report Yanagaki, Mitsuru Shiba, Hiroaki Hagiwara, Shin Hoshino, Masato Sakuda, Hitoshi Furukawa, Yoshiyuki Yanaga, Katsuhiko Int J Surg Case Rep Article BACKGROUND: Lemmel syndrome is a rare condition that leads to cholangitis and/or pancreatitis due to intraduodenal diverticulum. Surgery is considered for the treatment of severe or repeated symptoms in patients with this condition. CASE PRESENTATION: An 81-year-old woman was admitted to our hospital, complaining of general fatigue, BT 38.8 degree, and right hypochondoralgia. Her hepatobiliary enzyme levels were elevated, and enhanced abdominal computed tomography revealed dilation of the common bile duct and intraduodenal diverticulum. After restarting oral intake, her symptoms were exacerbated. Endoscopic retrograde cholangio-pancreatography (ERCP) revealed pancreaticobiliary maljunction and parapapillary diverticulum. Under a diagnosis of Lemmel syndrome with pancreaticobiliary maljunction complicated by acute pancreatitis and cholangitis, we performed extrahepatic bile duct resection with cholecystectomy and papilloplasty. Her postoperative course was uneventful, and the patient was discharged 20 days after surgery. She remains well at 5 months after surgery. CONCLUSION: We herein report a successfully diagnosed and treated case of Lemmel syndrome with pancreaticobiliary maljunction. Elsevier 2020-06-24 /pmc/articles/PMC7327874/ /pubmed/32698288 http://dx.doi.org/10.1016/j.ijscr.2020.06.080 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yanagaki, Mitsuru Shiba, Hiroaki Hagiwara, Shin Hoshino, Masato Sakuda, Hitoshi Furukawa, Yoshiyuki Yanaga, Katsuhiko A successfully treated case of Lemmel syndrome with pancreaticobiliary maljunction: A case report |
title | A successfully treated case of Lemmel syndrome with pancreaticobiliary maljunction: A case report |
title_full | A successfully treated case of Lemmel syndrome with pancreaticobiliary maljunction: A case report |
title_fullStr | A successfully treated case of Lemmel syndrome with pancreaticobiliary maljunction: A case report |
title_full_unstemmed | A successfully treated case of Lemmel syndrome with pancreaticobiliary maljunction: A case report |
title_short | A successfully treated case of Lemmel syndrome with pancreaticobiliary maljunction: A case report |
title_sort | successfully treated case of lemmel syndrome with pancreaticobiliary maljunction: a case report |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327874/ https://www.ncbi.nlm.nih.gov/pubmed/32698288 http://dx.doi.org/10.1016/j.ijscr.2020.06.080 |
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