Two cases of pancreatic neuroendocrine tumors with ectopic ACTH syndrome during their disease course

被引：0

作者：

Masatoshi Murakami

Keisuke Hirahata

Nao Fujimori

Takeo Yamamoto

Yoshinao Oda

Shingo Kozono

Keijiro Ueda

Testuhide Ito

Masafumi Nakamura

Yoshihiro Ogawa

机构：

[1] Kyushu University,Department of Medicine and Bioregulatory Science, Graduate School of Medical Sciences

[2] Kyushu University,Department of Anatomic Pathology, Pathological Sciences, Graduate School of Medical Sciences

[3] Kitakyushu Municipal Medical Center,Department of Surgery

[4] Fukuoka Sanno Hospital,Neuroendocrine Tumor Centre

[5] International University of Health and Welfare,Department of Gastroenterology, Graduate School of Medical Sciences

[6] Kyushu University,Department of Surgery and Oncology, Graduate School of Medical Sciences

来源：

Clinical Journal of Gastroenterology | 2024年 / 17卷

关键词：

Pancreatic neuroendocrine tumor; Ectopic ACTH syndrome; Cushing’s syndrome; PTHrP; Secondary hormone secretion;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Pancreatic neuroendocrine tumors (PanNETs) are rare malignant tumors that occur in the pancreas. They are divided into functioning and non-functioning tumors based on the presence or absence of their specific hormonal hyper-expression symptoms. Adrenocorticotropic hormone (ACTH)-producing PanNETs are rare, functional tumors, and their clinical characteristics and outcomes have not been well reported.

引用

页码：363 / 370

页数：7

共 50 条

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