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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Main Authors: Pak Chiu Wong, Wong Hoi She, Ui Soon Khoo, Tan To Cheung
Format: Article
Language:English
Published: Karger Publishers 2021-02-01
Series:Case Reports in Oncology
Subjects:
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.
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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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