Primary Hepatic Neuroendocrine Tumor: A Case Report and Literature Review

被引：7

作者：

Elayan, Ahmad ^{[1
]}

Batah, Hamzeh ^{[1
]}

Badawi, Moath ^{[2
]}

Saadeh, Ahmad ^{[3
]}

Hafez, Sufian Abdel ^{[4
]}

机构：

[1] Jordan Minist Hlth, Radiol, Amman, Jordan

[2] Jordan Minist Hlth, Pathol, Amman, Jordan

[3] Univ Jordan, Fac Med, Gen Practice, Amman, Jordan

[4] Univ Jordan, Fac Med, Internal Med, Amman, Jordan

来源：

CUREUS JOURNAL OF MEDICAL SCIENCE | 2022年 / 14卷 / 02期

关键词：

surgical case report; immunohistochemistry staining; zollinger-ellison syndrome; solitary hepatic mass; primary neuroendocrine tumor; LIVER;

D O I：

10.7759/cureus.22370

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Primary hepatic neuroendocrine tumors (PHNETs) are an utterly rare subtype of neuroendocrine tumors (NETs) that arise from cells of the neuroendocrine system. Due to the rarity and lack of distinctive radiological features, diagnosis and management of this tumor are challenging. Herein, we report a case of PHNET in a 19-year-old previously healthy female patient whose diagnosis was confirmed by histopathology and immunohistochemistry. This case emphasizes the importance of considering PHNETs in the differential diagnosis of a hepatic mass, management of patients with this disease, and post-operative follow-up.

引用

页数：5

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