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A Case of Primary Hepatic Neuroendocrine Tumor and Literature Review

We report an unusual presentation of primary hepatic neuroendocrine tumor which was initially misdiagnosed as intrahepatic cholangiocarcinoma. The diagnosis was only revealed after a major liver resection by histopathology. With adjuvant lanreotide injection, the patient survived for more than 16 mo...

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Detalles Bibliográficos
Autores principales: Wong, Pak Chiu, She, Wong Hoi, Khoo, Ui Soon, Cheung, Tan To
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983612/
https://www.ncbi.nlm.nih.gov/pubmed/33776688
http://dx.doi.org/10.1159/000510935
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author Wong, Pak Chiu
She, Wong Hoi
Khoo, Ui Soon
Cheung, Tan To
author_facet Wong, Pak Chiu
She, Wong Hoi
Khoo, Ui Soon
Cheung, Tan To
author_sort Wong, Pak Chiu
collection PubMed
description We report an unusual presentation of primary hepatic neuroendocrine tumor which was initially misdiagnosed as intrahepatic cholangiocarcinoma. The diagnosis was only revealed after a major liver resection by histopathology. With adjuvant lanreotide injection, the patient survived for more than 16 months after the operation without tumor recurrence. Diagnosis of this rare tumor has been a major challenge and we emphasize the importance of a preoperative diagnosis. Surgical resection remains the mainstay for curative treatment, while peptide receptor radionuclide therapy is an emerging treatment option which has provided promising results.
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spelling pubmed-79836122021-03-26 A Case of Primary Hepatic Neuroendocrine Tumor and Literature Review Wong, Pak Chiu She, Wong Hoi Khoo, Ui Soon Cheung, Tan To Case Rep Oncol Case Report We report an unusual presentation of primary hepatic neuroendocrine tumor which was initially misdiagnosed as intrahepatic cholangiocarcinoma. The diagnosis was only revealed after a major liver resection by histopathology. With adjuvant lanreotide injection, the patient survived for more than 16 months after the operation without tumor recurrence. Diagnosis of this rare tumor has been a major challenge and we emphasize the importance of a preoperative diagnosis. Surgical resection remains the mainstay for curative treatment, while peptide receptor radionuclide therapy is an emerging treatment option which has provided promising results. S. Karger AG 2021-02-25 /pmc/articles/PMC7983612/ /pubmed/33776688 http://dx.doi.org/10.1159/000510935 Text en Copyright © 2021 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Wong, Pak Chiu
She, Wong Hoi
Khoo, Ui Soon
Cheung, Tan To
A Case of Primary Hepatic Neuroendocrine Tumor and Literature Review
title A Case of Primary Hepatic Neuroendocrine Tumor and Literature Review
title_full A Case of Primary Hepatic Neuroendocrine Tumor and Literature Review
title_fullStr A Case of Primary Hepatic Neuroendocrine Tumor and Literature Review
title_full_unstemmed A Case of Primary Hepatic Neuroendocrine Tumor and Literature Review
title_short A Case of Primary Hepatic Neuroendocrine Tumor and Literature Review
title_sort case of primary hepatic neuroendocrine tumor and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983612/
https://www.ncbi.nlm.nih.gov/pubmed/33776688
http://dx.doi.org/10.1159/000510935
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