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Duodenal gangliocytic paraganglioma with lymph node metastases: A case report and comparative review of 31 cases

Gangliocytic paraganglioma (GP) is a rare tumor of uncertain origin most often located in the second portion of the duodenum. It is composed of three cellular components: Epithelioid endocrine cells, spindle-like/sustentacular cells, and ganglion-like cells. While this tumor most often behaves in a...

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Autores principales: Cathcart, Sahara J, Sasson, Aaron R, Kozel, Jessica A, Oliveto, Jennifer M, Ly, Quan P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480070/
https://www.ncbi.nlm.nih.gov/pubmed/28685135
http://dx.doi.org/10.12998/wjcc.v5.i6.222
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author Cathcart, Sahara J
Sasson, Aaron R
Kozel, Jessica A
Oliveto, Jennifer M
Ly, Quan P
author_facet Cathcart, Sahara J
Sasson, Aaron R
Kozel, Jessica A
Oliveto, Jennifer M
Ly, Quan P
author_sort Cathcart, Sahara J
collection PubMed
description Gangliocytic paraganglioma (GP) is a rare tumor of uncertain origin most often located in the second portion of the duodenum. It is composed of three cellular components: Epithelioid endocrine cells, spindle-like/sustentacular cells, and ganglion-like cells. While this tumor most often behaves in a benign manner, cases with metastasis are reported. We describe the case of a 62-year-old male with a periampullary GP with metastases to two regional lymph nodes who was successfully treated with pancreaticoduodenectomy. Using PubMed, EMBASE, EBSCOhost MEDLINE and CINAHL, and Google Scholar, we searched the literature for cases of GP with regional lymph node metastasis and evaluated the varying presentations, diagnostic workup, and disease management of identified cases. Thirty-one cases of GP with metastasis were compiled (30 with at least lymph node metastases and one with only distant metastasis to bone), with age at diagnosis ranging from 16 to 74 years. Ratio of males to females was 19:12. The most common presenting symptoms were abdominal pain (55%) and gastrointestinal bleeding or sequelae (42%). Twenty-five patients underwent pancreaticoduodenectomy. Five patients were treated with local resection alone. One patient died secondary to metastatic disease, and one died secondary to perioperative decompensation. The remainder did well, with no evidence of disease at follow-up from the most recent procedure (except two in which residual disease was deliberately left behind). Of the 26 cases with sufficient histological description, 16 described a primary tumor that infiltrated deep to the submucosa, and 3 described lymphovascular invasion. Of the specific immunohistochemistry staining patterns studied, synaptophysin (SYN) stained all epithelioid endocrine cells (18/18). Neuron specific enolase (NSE) and SYN stained most ganglion-like cells (7/8 and 13/18 respectively), and S-100 stained all spindle-like/sustentacular cells (21/21). Our literature review of published cases of GP with lymph node metastasis underscores the excellent prognosis of GP regardless of specific treatment modality. We question the necessity of aggressive surgical intervention in select patients, and argue that local resection of the mass and metastasis may be adequate. We also emphasize the importance of pre-surgical assessment with imaging studies, as well as post-surgical follow-up surveillance for disease recurrence.
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spelling pubmed-54800702017-07-06 Duodenal gangliocytic paraganglioma with lymph node metastases: A case report and comparative review of 31 cases Cathcart, Sahara J Sasson, Aaron R Kozel, Jessica A Oliveto, Jennifer M Ly, Quan P World J Clin Cases Case Report Gangliocytic paraganglioma (GP) is a rare tumor of uncertain origin most often located in the second portion of the duodenum. It is composed of three cellular components: Epithelioid endocrine cells, spindle-like/sustentacular cells, and ganglion-like cells. While this tumor most often behaves in a benign manner, cases with metastasis are reported. We describe the case of a 62-year-old male with a periampullary GP with metastases to two regional lymph nodes who was successfully treated with pancreaticoduodenectomy. Using PubMed, EMBASE, EBSCOhost MEDLINE and CINAHL, and Google Scholar, we searched the literature for cases of GP with regional lymph node metastasis and evaluated the varying presentations, diagnostic workup, and disease management of identified cases. Thirty-one cases of GP with metastasis were compiled (30 with at least lymph node metastases and one with only distant metastasis to bone), with age at diagnosis ranging from 16 to 74 years. Ratio of males to females was 19:12. The most common presenting symptoms were abdominal pain (55%) and gastrointestinal bleeding or sequelae (42%). Twenty-five patients underwent pancreaticoduodenectomy. Five patients were treated with local resection alone. One patient died secondary to metastatic disease, and one died secondary to perioperative decompensation. The remainder did well, with no evidence of disease at follow-up from the most recent procedure (except two in which residual disease was deliberately left behind). Of the 26 cases with sufficient histological description, 16 described a primary tumor that infiltrated deep to the submucosa, and 3 described lymphovascular invasion. Of the specific immunohistochemistry staining patterns studied, synaptophysin (SYN) stained all epithelioid endocrine cells (18/18). Neuron specific enolase (NSE) and SYN stained most ganglion-like cells (7/8 and 13/18 respectively), and S-100 stained all spindle-like/sustentacular cells (21/21). Our literature review of published cases of GP with lymph node metastasis underscores the excellent prognosis of GP regardless of specific treatment modality. We question the necessity of aggressive surgical intervention in select patients, and argue that local resection of the mass and metastasis may be adequate. We also emphasize the importance of pre-surgical assessment with imaging studies, as well as post-surgical follow-up surveillance for disease recurrence. Baishideng Publishing Group Inc 2017-06-16 2017-06-16 /pmc/articles/PMC5480070/ /pubmed/28685135 http://dx.doi.org/10.12998/wjcc.v5.i6.222 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Case Report
Cathcart, Sahara J
Sasson, Aaron R
Kozel, Jessica A
Oliveto, Jennifer M
Ly, Quan P
Duodenal gangliocytic paraganglioma with lymph node metastases: A case report and comparative review of 31 cases
title Duodenal gangliocytic paraganglioma with lymph node metastases: A case report and comparative review of 31 cases
title_full Duodenal gangliocytic paraganglioma with lymph node metastases: A case report and comparative review of 31 cases
title_fullStr Duodenal gangliocytic paraganglioma with lymph node metastases: A case report and comparative review of 31 cases
title_full_unstemmed Duodenal gangliocytic paraganglioma with lymph node metastases: A case report and comparative review of 31 cases
title_short Duodenal gangliocytic paraganglioma with lymph node metastases: A case report and comparative review of 31 cases
title_sort duodenal gangliocytic paraganglioma with lymph node metastases: a case report and comparative review of 31 cases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480070/
https://www.ncbi.nlm.nih.gov/pubmed/28685135
http://dx.doi.org/10.12998/wjcc.v5.i6.222
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