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Imaging and pathological features of primary hepatic neuroendocrine carcinoma: An analysis of nine cases and review of the literature

The present study aimed to analyze the imaging features and pathological basis of primary hepatic neuroendocrine carcinoma (PHNEC). A retrospective analysis of the imaging and pathological features of nine PHNEC cases was carried out at The Second Xiangya Hospital of Central South University (Changs...

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Autores principales: CHEN, ZHU, XIAO, HUA-EN, RAMCHANDRA, PAUDEL, HUANG, HAI-JIANG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961293/
https://www.ncbi.nlm.nih.gov/pubmed/24944650
http://dx.doi.org/10.3892/ol.2014.1844
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author CHEN, ZHU
XIAO, HUA-EN
RAMCHANDRA, PAUDEL
HUANG, HAI-JIANG
author_facet CHEN, ZHU
XIAO, HUA-EN
RAMCHANDRA, PAUDEL
HUANG, HAI-JIANG
author_sort CHEN, ZHU
collection PubMed
description The present study aimed to analyze the imaging features and pathological basis of primary hepatic neuroendocrine carcinoma (PHNEC). A retrospective analysis of the imaging and pathological features of nine PHNEC cases was carried out at The Second Xiangya Hospital of Central South University (Changsha, China). The nine patients were subjected to dynamic contrast-enhanced computed tomography (CT) scanning of the liver and pathological diagnosis of the tissue samples. In addition, two patients were subjected to magnetic resonance imaging (MRI). CT scanning revealed the presence of single or multiple masses in the liver with a maximum diameter of 1–10 cm. These hepatic masses were of low density as showed by plain CT. These masses showed uneven or annular enhancement at their margins in the arterial phase. The venous portal phase showed consistent or declined enhancement and the delayed phase showed light enhancement in these masses. In addition, multiple intrahepatic nodules with long T1 and T2 signal intensities and obvious enhancement were observed by MRI in one patient, while intrahepatic lesions with moderate length T2 signal intensities and light enhancement not visible on the T1 image were observed in another patient. Pathological analysis revealed that the tumor cells exhibited morphological diversity. Immunohistochemical staining revealed that the tumor cells were chromogranin A- and synaptophysin-positive, and carcinoembryonic antigen-, hepatocytic antigen- and α-fetoprotein-negative. Imaging methods, including CT and MRI, are useful for the diagnosis of PHNEC; however, pathological examination is required for a final, definite diagnosis.
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spelling pubmed-39612932014-06-18 Imaging and pathological features of primary hepatic neuroendocrine carcinoma: An analysis of nine cases and review of the literature CHEN, ZHU XIAO, HUA-EN RAMCHANDRA, PAUDEL HUANG, HAI-JIANG Oncol Lett Articles The present study aimed to analyze the imaging features and pathological basis of primary hepatic neuroendocrine carcinoma (PHNEC). A retrospective analysis of the imaging and pathological features of nine PHNEC cases was carried out at The Second Xiangya Hospital of Central South University (Changsha, China). The nine patients were subjected to dynamic contrast-enhanced computed tomography (CT) scanning of the liver and pathological diagnosis of the tissue samples. In addition, two patients were subjected to magnetic resonance imaging (MRI). CT scanning revealed the presence of single or multiple masses in the liver with a maximum diameter of 1–10 cm. These hepatic masses were of low density as showed by plain CT. These masses showed uneven or annular enhancement at their margins in the arterial phase. The venous portal phase showed consistent or declined enhancement and the delayed phase showed light enhancement in these masses. In addition, multiple intrahepatic nodules with long T1 and T2 signal intensities and obvious enhancement were observed by MRI in one patient, while intrahepatic lesions with moderate length T2 signal intensities and light enhancement not visible on the T1 image were observed in another patient. Pathological analysis revealed that the tumor cells exhibited morphological diversity. Immunohistochemical staining revealed that the tumor cells were chromogranin A- and synaptophysin-positive, and carcinoembryonic antigen-, hepatocytic antigen- and α-fetoprotein-negative. Imaging methods, including CT and MRI, are useful for the diagnosis of PHNEC; however, pathological examination is required for a final, definite diagnosis. D.A. Spandidos 2014-04 2014-01-31 /pmc/articles/PMC3961293/ /pubmed/24944650 http://dx.doi.org/10.3892/ol.2014.1844 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
CHEN, ZHU
XIAO, HUA-EN
RAMCHANDRA, PAUDEL
HUANG, HAI-JIANG
Imaging and pathological features of primary hepatic neuroendocrine carcinoma: An analysis of nine cases and review of the literature
title Imaging and pathological features of primary hepatic neuroendocrine carcinoma: An analysis of nine cases and review of the literature
title_full Imaging and pathological features of primary hepatic neuroendocrine carcinoma: An analysis of nine cases and review of the literature
title_fullStr Imaging and pathological features of primary hepatic neuroendocrine carcinoma: An analysis of nine cases and review of the literature
title_full_unstemmed Imaging and pathological features of primary hepatic neuroendocrine carcinoma: An analysis of nine cases and review of the literature
title_short Imaging and pathological features of primary hepatic neuroendocrine carcinoma: An analysis of nine cases and review of the literature
title_sort imaging and pathological features of primary hepatic neuroendocrine carcinoma: an analysis of nine cases and review of the literature
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961293/
https://www.ncbi.nlm.nih.gov/pubmed/24944650
http://dx.doi.org/10.3892/ol.2014.1844
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