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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2021
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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. |
format | Online Article Text |
id | pubmed-7983612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
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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