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原发性肝神经内分泌肿瘤:一种罕见的实体瘤。

Primary hepatic neuroendocrine tumor: A rare entity.

作者信息

Jain Richa D, Sakpal Mallikarjun, Asthana Sonal, Shankar Mythri, Agarwal Vijay, Mn Vidya, Panchal Nijalingappa, Raichurkar Karthik, Kale Sudhir

机构信息

Department of Radiodiagnosis, Aster CMI Hospital, Bengaluru, India.

Department of Hepatobiliary Sciences, Aster CMI Hospital, Bengaluru, India.

出版信息

Radiol Case Rep. 2020 Sep 17;15(11):2362-2366. doi: 10.1016/j.radcr.2020.09.011. eCollection 2020 Nov.

Abstract

Liver is the most common site for neuroendocrine metastasis. However, primary neuroendocrine tumor is a rare focal hepatic lesion with a better prognosis than hepatocellular carcinoma and other malignant hepatic lesions. We present a case of primary hepatic neuroendocrine tumor in a 38-year-old female patient with a radiological diagnosis of atypical focal hepatic lesion, and a confirmed diagnosis on histopathology. Few radiology features like predominant cystic component with absence of focal lesion at any other site, aids the imaging diagnosis of primary hepatic neuroendocrine tumor.

摘要

肝脏是神经内分泌转移最常见的部位。然而,原发性神经内分泌肿瘤是一种罕见的肝脏局灶性病变,其预后比肝细胞癌和其他肝脏恶性病变要好。我们报告一例38岁女性原发性肝脏神经内分泌肿瘤病例,该病例经放射学诊断为非典型肝脏局灶性病变,并经组织病理学确诊。一些放射学特征,如以囊性成分为主且其他任何部位均无局灶性病变,有助于原发性肝脏神经内分泌肿瘤的影像诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c207/7502789/fef6065e0085/gr1.jpg

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