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Schwannoma mimicking pancreatic carcinoma: A case report

BACKGROUND: Schwannoma of the pancreas is extremely rare. We report a case of pancreatic schwannoma that was difficult to distinguish from pancreatic carcinoma before surgery. CASE SUMMARY: A 66-year-old male underwent a right-lobe hepatectomy for hepatocellular carcinoma. Post-surgical computed tom...

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Autores principales: Kimura, Koichi, Adachi, Eisuke, Toyohara, Ayako, Omori, Sachie, Ezaki, Kaoru, Ihara, Ryo, Higashi, Takahiro, Ohgaki, Kippei, Ito, Shuhei, Maehara, Shin-ichiro, Nakamura, Toshihiko, Fushimi, Fumiyoshi, Maehara, Yoshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173407/
https://www.ncbi.nlm.nih.gov/pubmed/34141813
http://dx.doi.org/10.12998/wjcc.v9.i17.4453
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author Kimura, Koichi
Adachi, Eisuke
Toyohara, Ayako
Omori, Sachie
Ezaki, Kaoru
Ihara, Ryo
Higashi, Takahiro
Ohgaki, Kippei
Ito, Shuhei
Maehara, Shin-ichiro
Nakamura, Toshihiko
Fushimi, Fumiyoshi
Maehara, Yoshihiko
author_facet Kimura, Koichi
Adachi, Eisuke
Toyohara, Ayako
Omori, Sachie
Ezaki, Kaoru
Ihara, Ryo
Higashi, Takahiro
Ohgaki, Kippei
Ito, Shuhei
Maehara, Shin-ichiro
Nakamura, Toshihiko
Fushimi, Fumiyoshi
Maehara, Yoshihiko
author_sort Kimura, Koichi
collection PubMed
description BACKGROUND: Schwannoma of the pancreas is extremely rare. We report a case of pancreatic schwannoma that was difficult to distinguish from pancreatic carcinoma before surgery. CASE SUMMARY: A 66-year-old male underwent a right-lobe hepatectomy for hepatocellular carcinoma. Post-surgical computed tomography showed a 10 mm long solid mass with ischemia, with no expansion into the main pancreatic duct. Upon magnetic resonance cholangiopancreatography, the tumor had high signal intensity in diffusion weighted images, consistent with pancreatic carcinoma. Endoscopic ultrasound (EUS) was performed to obtain more information about the tumor, and showed a 14 mm solid and hypoechoic mass in the pancreatic body. Contrast enhanced EUS revealed that the tumor showed a hyperechoic mass in the early phase, and the contrasting effect continuation was very short; findings also consistent with pancreatic carcinoma. Thus, we preoperatively diagnosed his condition as a pancreatic carcinoma and performed distal pancreatectomy with splenectomy. Microscopic examination showed that the tumor was in fact a benign schwannoma. Histology showed a proliferation of spindle-shaped cell in a vague fascicular and haphazard pattern, with palisading arrangement. CONCLUSION: Schwannoma of the pancreas is very rare, however, clinicians should consider schwannoma as the differential diagnosis for pancreatic tumors.
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spelling pubmed-81734072021-06-16 Schwannoma mimicking pancreatic carcinoma: A case report Kimura, Koichi Adachi, Eisuke Toyohara, Ayako Omori, Sachie Ezaki, Kaoru Ihara, Ryo Higashi, Takahiro Ohgaki, Kippei Ito, Shuhei Maehara, Shin-ichiro Nakamura, Toshihiko Fushimi, Fumiyoshi Maehara, Yoshihiko World J Clin Cases Case Report BACKGROUND: Schwannoma of the pancreas is extremely rare. We report a case of pancreatic schwannoma that was difficult to distinguish from pancreatic carcinoma before surgery. CASE SUMMARY: A 66-year-old male underwent a right-lobe hepatectomy for hepatocellular carcinoma. Post-surgical computed tomography showed a 10 mm long solid mass with ischemia, with no expansion into the main pancreatic duct. Upon magnetic resonance cholangiopancreatography, the tumor had high signal intensity in diffusion weighted images, consistent with pancreatic carcinoma. Endoscopic ultrasound (EUS) was performed to obtain more information about the tumor, and showed a 14 mm solid and hypoechoic mass in the pancreatic body. Contrast enhanced EUS revealed that the tumor showed a hyperechoic mass in the early phase, and the contrasting effect continuation was very short; findings also consistent with pancreatic carcinoma. Thus, we preoperatively diagnosed his condition as a pancreatic carcinoma and performed distal pancreatectomy with splenectomy. Microscopic examination showed that the tumor was in fact a benign schwannoma. Histology showed a proliferation of spindle-shaped cell in a vague fascicular and haphazard pattern, with palisading arrangement. CONCLUSION: Schwannoma of the pancreas is very rare, however, clinicians should consider schwannoma as the differential diagnosis for pancreatic tumors. Baishideng Publishing Group Inc 2021-06-16 2021-06-16 /pmc/articles/PMC8173407/ /pubmed/34141813 http://dx.doi.org/10.12998/wjcc.v9.i17.4453 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (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
Kimura, Koichi
Adachi, Eisuke
Toyohara, Ayako
Omori, Sachie
Ezaki, Kaoru
Ihara, Ryo
Higashi, Takahiro
Ohgaki, Kippei
Ito, Shuhei
Maehara, Shin-ichiro
Nakamura, Toshihiko
Fushimi, Fumiyoshi
Maehara, Yoshihiko
Schwannoma mimicking pancreatic carcinoma: A case report
title Schwannoma mimicking pancreatic carcinoma: A case report
title_full Schwannoma mimicking pancreatic carcinoma: A case report
title_fullStr Schwannoma mimicking pancreatic carcinoma: A case report
title_full_unstemmed Schwannoma mimicking pancreatic carcinoma: A case report
title_short Schwannoma mimicking pancreatic carcinoma: A case report
title_sort schwannoma mimicking pancreatic carcinoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173407/
https://www.ncbi.nlm.nih.gov/pubmed/34141813
http://dx.doi.org/10.12998/wjcc.v9.i17.4453
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