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Pancreaticopleural fistula in a child with chronic pancreatitis harboring compound SPINK1 variants

BACKGROUND: Pancreaticopleural fistula (PPF) is a rare complication of chronic pancreatitis (CP) that requires a high index of clinical suspicion in the patient who presents with a pleural effusion. Visualizing the fistula tract from the pancreatic duct to the pleural space by radiological imaging p...

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Autores principales: Kijmassuwan, Teera, Aanpreung, Prapun, Prachayakul, Varayu, Tovichien, Prakarn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8199822/
https://www.ncbi.nlm.nih.gov/pubmed/34118876
http://dx.doi.org/10.1186/s12876-021-01842-1
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author Kijmassuwan, Teera
Aanpreung, Prapun
Prachayakul, Varayu
Tovichien, Prakarn
author_facet Kijmassuwan, Teera
Aanpreung, Prapun
Prachayakul, Varayu
Tovichien, Prakarn
author_sort Kijmassuwan, Teera
collection PubMed
description BACKGROUND: Pancreaticopleural fistula (PPF) is a rare complication of chronic pancreatitis (CP) that requires a high index of clinical suspicion in the patient who presents with a pleural effusion. Visualizing the fistula tract from the pancreatic duct to the pleural space by radiological imaging provides confirmation of this complication. CASE PRESENTATION: A 9-year-old boy who presented with massive right pleural effusion secondary to PPF, a complication of CP from a genetic mutation involving two mutations of SPINK1. We successfully managed the case with by endoscopic pancreatic duct stent placement after failure of conservative treatment approaches. CONCLUSIONS: PPF is a rare but serious complication of CP in all ages. The diagnosis of PPF in children requires a high index of clinical suspicion and should be considered in the differential diagnosis of massive pleural effusion where pancreatic pathology is present. A high level of pleural fluid amylase and the results from radiological imaging when the patients have symptoms play essential roles in the diagnosis of PPF. Currently, Magnetic resonance cholangiopancreatigraphy (MRCP) is the imaging modality of choice. Endoscopic therapy and surgery are treatment options for patients who do not respond to conservative therapy.
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spelling pubmed-81998222021-06-15 Pancreaticopleural fistula in a child with chronic pancreatitis harboring compound SPINK1 variants Kijmassuwan, Teera Aanpreung, Prapun Prachayakul, Varayu Tovichien, Prakarn BMC Gastroenterol Case Report BACKGROUND: Pancreaticopleural fistula (PPF) is a rare complication of chronic pancreatitis (CP) that requires a high index of clinical suspicion in the patient who presents with a pleural effusion. Visualizing the fistula tract from the pancreatic duct to the pleural space by radiological imaging provides confirmation of this complication. CASE PRESENTATION: A 9-year-old boy who presented with massive right pleural effusion secondary to PPF, a complication of CP from a genetic mutation involving two mutations of SPINK1. We successfully managed the case with by endoscopic pancreatic duct stent placement after failure of conservative treatment approaches. CONCLUSIONS: PPF is a rare but serious complication of CP in all ages. The diagnosis of PPF in children requires a high index of clinical suspicion and should be considered in the differential diagnosis of massive pleural effusion where pancreatic pathology is present. A high level of pleural fluid amylase and the results from radiological imaging when the patients have symptoms play essential roles in the diagnosis of PPF. Currently, Magnetic resonance cholangiopancreatigraphy (MRCP) is the imaging modality of choice. Endoscopic therapy and surgery are treatment options for patients who do not respond to conservative therapy. BioMed Central 2021-06-12 /pmc/articles/PMC8199822/ /pubmed/34118876 http://dx.doi.org/10.1186/s12876-021-01842-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Kijmassuwan, Teera
Aanpreung, Prapun
Prachayakul, Varayu
Tovichien, Prakarn
Pancreaticopleural fistula in a child with chronic pancreatitis harboring compound SPINK1 variants
title Pancreaticopleural fistula in a child with chronic pancreatitis harboring compound SPINK1 variants
title_full Pancreaticopleural fistula in a child with chronic pancreatitis harboring compound SPINK1 variants
title_fullStr Pancreaticopleural fistula in a child with chronic pancreatitis harboring compound SPINK1 variants
title_full_unstemmed Pancreaticopleural fistula in a child with chronic pancreatitis harboring compound SPINK1 variants
title_short Pancreaticopleural fistula in a child with chronic pancreatitis harboring compound SPINK1 variants
title_sort pancreaticopleural fistula in a child with chronic pancreatitis harboring compound spink1 variants
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8199822/
https://www.ncbi.nlm.nih.gov/pubmed/34118876
http://dx.doi.org/10.1186/s12876-021-01842-1
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