Primary hepatic neuroendocrine tumor

Summary Primary hepatic neuroendocrine tumor (PHNET) is a rare type of neuroendocrine tumor (NET) that is also a primary hepatic tumor. Patients are present with almost no specific clinical symptoms and typically present with negative test results and atypical imaging characteristics; therefore, the...

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Published in:Endocrinology, diabetes & metabolism case reports Vol. 2021; no. 1; pp. 1 - 7
Main Authors: Tuan Linh, Le, Minh Duc, Nguyen, Tu Minh, Hoang, Ngoc Cuong, Nguyen, Thu Ha, Vuong, Luan, Dao-Thi, Tra My, Thieu-Thi, Van Lenh, Bui
Format: Journal Article
Language:English
Published: England Bioscientifica Ltd 01-06-2021
Bioscientifica
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Summary:Summary Primary hepatic neuroendocrine tumor (PHNET) is a rare type of neuroendocrine tumor (NET) that is also a primary hepatic tumor. Patients are present with almost no specific clinical symptoms and typically present with negative test results and atypical imaging characteristics; therefore, the differentiation of PHNET from other types of primary hepatic masses can be very difficult. In this article, we describe a case of PHNET that mimicked a liver helminth infection in a 57-year-old man. The diagnosis of PHNET in this patient was challenging, and the final diagnosis was based on imaging, histopathology features, and long-term follow-up. Learning points An uncommon type of neuroendocrine tumor (NET) is a primary hepatic neuroendocrine tumor (PHNET). Primary hepatic neuroendocrine tumors are rare NET lesions found in the liver, characterized by non-specific clinical and imaging results, which can be easily confused with other liver lesions, including HCC and parasitic lesions. To have a conclusive diagnosis and classification, a mixture of many medical assessment techniques, such as imaging, gastrointestinal endoscopy, nuclear medicine, anatomy, including histopathology, and immunohistochemistry, is essential.
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L T Linh and N M Duc contributed equally to this work
ISSN:2052-0573
2052-0573
DOI:10.1530/EDM-20-0220