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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Format: | Article |
Language: | English |
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Karger Publishers
2021-02-01
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Series: | Case Reports in Oncology |
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Online Access: | https://www.karger.com/Article/FullText/510935 |
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author | Pak Chiu Wong Wong Hoi She Ui Soon Khoo Tan To Cheung |
author_facet | Pak Chiu Wong Wong Hoi She Ui Soon Khoo Tan To Cheung |
author_sort | Pak Chiu Wong |
collection | DOAJ |
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. |
first_indexed | 2024-12-13T14:47:08Z |
format | Article |
id | doaj.art-a7b71e8bddd74c658fb55ffce7af7e41 |
institution | Directory Open Access Journal |
issn | 1662-6575 |
language | English |
last_indexed | 2024-12-13T14:47:08Z |
publishDate | 2021-02-01 |
publisher | Karger Publishers |
record_format | Article |
series | Case Reports in Oncology |
spelling | doaj.art-a7b71e8bddd74c658fb55ffce7af7e412022-12-21T23:41:27ZengKarger PublishersCase Reports in Oncology1662-65752021-02-01141909710.1159/000510935510935A Case of Primary Hepatic Neuroendocrine Tumor and Literature ReviewPak Chiu WongWong Hoi SheUi Soon KhooTan To CheungWe 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.https://www.karger.com/Article/FullText/510935primary hepatic neuroendocrine tumorliver neoplasmcarcinoid tumor |
spellingShingle | Pak Chiu Wong Wong Hoi She Ui Soon Khoo Tan To Cheung A Case of Primary Hepatic Neuroendocrine Tumor and Literature Review Case Reports in Oncology primary hepatic neuroendocrine tumor liver neoplasm carcinoid tumor |
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 | primary hepatic neuroendocrine tumor liver neoplasm carcinoid tumor |
url | https://www.karger.com/Article/FullText/510935 |
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