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Ampullary and Pancreatic Neuroendocrine Tumors: A Series of Cases and Review of the Literature

The ampulla of Vater is a unique, highly vascularized pouch. Its anatomic transition is halfway along the second part of the duodenum from the foregut to the midgut. According to the World Health Organization’s (WHO) latest nomenclature, carcinoid tumors are now called neuroendocrine tumors (NETs)....

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Autores principales: Matli, Venkata Vinod Kumar, Wellman, Gregory, Jaganmohan, Sathya, Koticha, Kirtan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793321/
https://www.ncbi.nlm.nih.gov/pubmed/35111492
http://dx.doi.org/10.7759/cureus.21657
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author Matli, Venkata Vinod Kumar
Wellman, Gregory
Jaganmohan, Sathya
Koticha, Kirtan
author_facet Matli, Venkata Vinod Kumar
Wellman, Gregory
Jaganmohan, Sathya
Koticha, Kirtan
author_sort Matli, Venkata Vinod Kumar
collection PubMed
description The ampulla of Vater is a unique, highly vascularized pouch. Its anatomic transition is halfway along the second part of the duodenum from the foregut to the midgut. According to the World Health Organization’s (WHO) latest nomenclature, carcinoid tumors are now called neuroendocrine tumors (NETs). Knowledge of NETs is important because of their rarity, reclassification, prognosis, and management. NETs involving the ampulla of Vater are extremely rare, constituting <0.05% of gastrointestinal NETs, and involving the pancreas are rare to our knowledge. There are only a few reports of ampullary NETs. We report two rare NET cases involving the ampulla and pancreas and review the relevant literature. A 71-year-old patient with neurofibromatosis and multiple comorbidities presented with chronic intermittent abdominal pain. Abdominal imaging studies showed a suspicious mass at the level of the ampulla. Endoscopic retrograde cholangiopancreatography and endoscopic ultrasound revealed bulging papillae. Histopathology of the biopsied mass revealed a low-grade NET. Given his multiple comorbidities, the patient was scheduled for endoscopic resection. Our second patient was an 83-year-old lady presenting with nausea and vomiting. Abdominal imaging studies revealed a lobular mass over the body of the pancreas. Histopathological examination of fine-needle aspiration of the mass confirmed a well-differentiated low-grade NET. Octreoscan and dotatate scans showed pancreatic, multiple hepatic and metastatic lesions in the left lung and left shoulder. The patient is currently stable after completing peptide receptor radioligand therapy at a tertiary oncology center. Because of the patients’ comorbidities and staging, their management has taken different approaches. More data and more research are needed for accurate assessment of prognosis; however, a review of the latest literature recommends Whipple resection with lymphadenectomy for all ampullary NETs provided patients can tolerate the procedure. Endoscopic resection or surgical ampullary resection should be performed on contraindicated patients. The majority of ampullary and pancreatic NETs would have metastasized by the time patients sought treatment. Because of their rarity and ill-defined and highly variable presentation, NET diagnosis is always delayed and sometimes incidental; therefore, we emphasize the importance of early diagnosis and management to reduce mortality and morbidity.
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spelling pubmed-87933212022-02-01 Ampullary and Pancreatic Neuroendocrine Tumors: A Series of Cases and Review of the Literature Matli, Venkata Vinod Kumar Wellman, Gregory Jaganmohan, Sathya Koticha, Kirtan Cureus Internal Medicine The ampulla of Vater is a unique, highly vascularized pouch. Its anatomic transition is halfway along the second part of the duodenum from the foregut to the midgut. According to the World Health Organization’s (WHO) latest nomenclature, carcinoid tumors are now called neuroendocrine tumors (NETs). Knowledge of NETs is important because of their rarity, reclassification, prognosis, and management. NETs involving the ampulla of Vater are extremely rare, constituting <0.05% of gastrointestinal NETs, and involving the pancreas are rare to our knowledge. There are only a few reports of ampullary NETs. We report two rare NET cases involving the ampulla and pancreas and review the relevant literature. A 71-year-old patient with neurofibromatosis and multiple comorbidities presented with chronic intermittent abdominal pain. Abdominal imaging studies showed a suspicious mass at the level of the ampulla. Endoscopic retrograde cholangiopancreatography and endoscopic ultrasound revealed bulging papillae. Histopathology of the biopsied mass revealed a low-grade NET. Given his multiple comorbidities, the patient was scheduled for endoscopic resection. Our second patient was an 83-year-old lady presenting with nausea and vomiting. Abdominal imaging studies revealed a lobular mass over the body of the pancreas. Histopathological examination of fine-needle aspiration of the mass confirmed a well-differentiated low-grade NET. Octreoscan and dotatate scans showed pancreatic, multiple hepatic and metastatic lesions in the left lung and left shoulder. The patient is currently stable after completing peptide receptor radioligand therapy at a tertiary oncology center. Because of the patients’ comorbidities and staging, their management has taken different approaches. More data and more research are needed for accurate assessment of prognosis; however, a review of the latest literature recommends Whipple resection with lymphadenectomy for all ampullary NETs provided patients can tolerate the procedure. Endoscopic resection or surgical ampullary resection should be performed on contraindicated patients. The majority of ampullary and pancreatic NETs would have metastasized by the time patients sought treatment. Because of their rarity and ill-defined and highly variable presentation, NET diagnosis is always delayed and sometimes incidental; therefore, we emphasize the importance of early diagnosis and management to reduce mortality and morbidity. Cureus 2022-01-27 /pmc/articles/PMC8793321/ /pubmed/35111492 http://dx.doi.org/10.7759/cureus.21657 Text en Copyright © 2022, Matli et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Matli, Venkata Vinod Kumar
Wellman, Gregory
Jaganmohan, Sathya
Koticha, Kirtan
Ampullary and Pancreatic Neuroendocrine Tumors: A Series of Cases and Review of the Literature
title Ampullary and Pancreatic Neuroendocrine Tumors: A Series of Cases and Review of the Literature
title_full Ampullary and Pancreatic Neuroendocrine Tumors: A Series of Cases and Review of the Literature
title_fullStr Ampullary and Pancreatic Neuroendocrine Tumors: A Series of Cases and Review of the Literature
title_full_unstemmed Ampullary and Pancreatic Neuroendocrine Tumors: A Series of Cases and Review of the Literature
title_short Ampullary and Pancreatic Neuroendocrine Tumors: A Series of Cases and Review of the Literature
title_sort ampullary and pancreatic neuroendocrine tumors: a series of cases and review of the literature
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793321/
https://www.ncbi.nlm.nih.gov/pubmed/35111492
http://dx.doi.org/10.7759/cureus.21657
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