Benign neuroendocrine and other rare benign tumors of the pancreas

被引：0

作者：

Happel, B. ^{[1
]}

Niederle, B. ^{[2
]}

Puespoek, A. ^{[3
]}

Ba-Ssalamah, A. ^{[1
]}

Schima, W. ^{[4
]}

机构：

[1] Med Univ Wien, Univ Klin Radiodiag, A-1090 Vienna, Austria

[2] Med Univ Wien, Univ Klin Chirurg, A-1090 Vienna, Austria

[3] Med Univ Wien, Univ Klin Inner Med 3, Klin Abt Gastroenterol & Hepatol, A-1090 Vienna, Austria

[4] KH Gottlicher Heiland, Abt Radiol & Bildgebende Diag, Vienna, Austria

来源：

RADIOLOGE | 2008年 / 48卷 / 08期

关键词：

neuroendocrine tumor; intrapancreatic accessory spleen; computed tomography (CT); magnetic resonance imaging (MRI); sonography; angiography;

D O I：

10.1007/s00117-008-1672-3

中图分类号：

R8 [特种医学]; R445 [影像诊断学];

学科分类号：

1002 ; 100207 ; 1009 ;

摘要：

Neuroendocrine tumors (NET) of the pancreas are rare neoplasms, which arise from cells of the islets of Langerhans. The most common NET are the insulinoma, gastrinoma and hormone inactive NET. Very rare entities are the schwannoma, leiomyoma, teratoma, intrapancreatic lipoma, hemangioma and the intrapancreatic accessory spleen. Essential for therapy, which in most cases is difficult, are an exact localization and various modalities of imaging diagnostics.

引用

页码：752 / 763

页数：12

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